2024
Hong, F., Aldhous, T. P., Kemmitt, P. D., & Bower, J. F. (2024). A directed enolization strategy enables by-product-free construction of contiguous stereocentres en route to complex amino acids.. Nature chemistry. doi:10.1038/s41557-024-01473-5DOI: 10.1038/s41557-024-01473-5
de Carvalho, R. L., Wood, J. M., Almeida, R. G., Berry, N. G., da Silva Júnior, E. N., & Bower, J. F. (2024). The Synthesis and Reactivity of Naphthoquinonynes.. Angewandte Chemie (International ed. in English), e202400188. doi:10.1002/anie.202400188DOI: 10.1002/anie.202400188
1,3,5,7-Tetramethyl-8-phenyl-2,4,6-trioxa-8-phosphatricyclo[3.3.1.13,7]decane (Chapter)
Adams, R., Pringle, P., & Bower, J. (2024). 1,3,5,7-Tetramethyl-8-phenyl-2,4,6-trioxa-8-phosphatricyclo[3.3.1.13,7]decane. In Encyclopedia of Reagents for Organic Synthesis. doi:10.1002/047084289X.rn02530DOI: 10.1002/047084289X.rn02530
2023
Smith, M. J. S., Tu, W., Robertson, C. M., & Bower, J. F. (2023). Stereospecific Aminative Cyclizations Triggered by Intermolecular Aza-Prilezhaev Alkene Aziridination.. Angewandte Chemie (International ed. in English), 62(48), e202312797. doi:10.1002/anie.202312797DOI: 10.1002/anie.202312797
Jing, C., Mao, W., & Bower, J. F. (2023). Iridium-Catalyzed Enantioselective Alkene Hydroalkylation via a Heteroaryl-Directed Enolization-Decarboxylation Sequence.. Journal of the American Chemical Society, 145(44), 23918-23924. doi:10.1021/jacs.3c10163DOI: 10.1021/jacs.3c10163
Scott, S. C., Cadge, J. A., Boden, G. K., Bower, J. F., & Russell, C. A. (2023). A Hemilabile NHC-Gold Complex and its Application to the Redox Neutral 1,2-Oxyarylation of Feedstock Alkenes. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 62(23). doi:10.1002/anie.202301526DOI: 10.1002/anie.202301526
Zhu, Y., Smith, M. J. S., Tu, W., & Bower, J. F. (2023). A Stereospecific Alkene 1,2-Aminofunctionalization Platform for the Assembly of Complex Nitrogen-Containing Ring Systems. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION. doi:10.1002/anie.202301262DOI: 10.1002/anie.202301262
C-C Bond Activations of Minimally Activated Cyclopropanes (Journal article)
Sokolova, O. O., Dalling, A. G., & Bower, J. F. (2023). C-C Bond Activations of Minimally Activated Cyclopropanes. SYNLETT, 34(12), 1317-1326. doi:10.1055/s-0042-1753177DOI: 10.1055/s-0042-1753177
2022
Cadge, J. A., Gates, P. J., Bower, J. F., & Russell, C. A. (2022). Migratory Insertion of CO into a Au-C Bond. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY. doi:10.1021/jacs.2c10432DOI: 10.1021/jacs.2c10432
Cooper, P., Dalling, A. G., Farrar, E. H. E., Aldhous, T. P., Grelaud, S., Lester, E., . . . Bower, J. F. (2022). Atom and step economical synthesis of acyclic quaternary centers <i>via</i> iridium-catalyzed hydroarylative cross-coupling of 1,1-disubstituted alkenes. CHEMICAL SCIENCE, 13(37), 11183-11189. doi:10.1039/d2sc02790aDOI: 10.1039/d2sc02790a
Jing, C., Jones, B. T., Adams, R. J., & Bower, J. F. (2022). Cyclopropane-Fused N-Heterocycles via Aza-Heck-Triggered C(sp<SUP>3</SUP>)-H Functionalization Cascades. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY. doi:10.1021/jacs.2c08304DOI: 10.1021/jacs.2c08304
Sokolova, O. O., & Bower, J. F. (2022). An <i>endo</i>-Directing-Group Strategy Unlocks Enantioselective (3+1+2) Carbonylative Cycloadditions of Aminocyclopropanes. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 61(32). doi:10.1002/anie.202205007DOI: 10.1002/anie.202205007
Calow, A. D. J., Dailler, D., & Bower, J. F. (2022). Carbonylative N-Heterocyclization via Nitrogen-Directed C-C Bond Activation of Nonactivated Cyclopropanes. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 144(25), 11069-11074. doi:10.1021/jacs.2c02921DOI: 10.1021/jacs.2c02921
Jardim, G. A. M., de Carvalho, R. L., Nunes, M. P., Machado, L. A., Almeida, L. D., Bahou, K. A., . . . da Silva Junior, E. N. (2022). Looking deep into C-H functionalization: the synthesis and application of cyclopentadienyl and related metal catalysts. CHEMICAL COMMUNICATIONS, 58(19), 3101-3121. doi:10.1039/d1cc07040aDOI: 10.1039/d1cc07040a
2021
O'Neil, L. G., & Bower, J. F. (2021). Electrophilic Aminating Agents in Total Synthesis. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 60(49), 25640-25666. doi:10.1002/anie.202102864DOI: 10.1002/anie.202102864
Cadge, J. A., Bower, J. F., & Russell, C. A. (2021). A Systematic Study of the Effects of Complex Structure on Aryl Iodide Oxidative Addition at Bipyridyl-Ligated Gold(I) Centers. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 60(47), 24976-24983. doi:10.1002/anie.202108744DOI: 10.1002/anie.202108744
Jing, C., Farndon, J. J., & Bower, J. F. (2021). Dearomatizing Amination Reactions. CHEMICAL RECORD, 21(10), 2909-2926. doi:10.1002/tcr.202100104DOI: 10.1002/tcr.202100104
Jones, B. T., Garcia-Carceles, J., Caiger, L., Hazelden, I. R., Lewis, R. J., Langer, T., & Bower, J. F. (2021). Complex Polyheterocycles and the Stereochemical Reassignment of Pileamartine A via Aza-Heck Triggered Aryl C-H Functionalization Cascades. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 143(38), 15593-15598. doi:10.1021/jacs.1c08615DOI: 10.1021/jacs.1c08615
Aldhous, T. P., Chung, R. W. M., Dalling, A. G., & Bower, J. F. (2021). Enantioselective Intermolecular Murai-Type Alkene Hydroarylation Reactions. SYNTHESIS-STUTTGART, 53(17), 2961-2975. doi:10.1055/s-0040-1720406DOI: 10.1055/s-0040-1720406
Sokolova, O. O., & Bower, J. F. (2021). Selective Carbon-Carbon Bond Cleavage of Cyclopropylamine Derivatives.. Chemical Reviews, 121(1), 80-109. doi:10.1021/acs.chemrev.0c00166DOI: 10.1021/acs.chemrev.0c00166
Naphthoquinones and Derivatives for Chemotherapy: Perspectives and Limitations of their Anti-trypanosomatids Activities (Journal article)
Dantas-Pereira, L., Cunha-Junior, E. F., Andrade-Neto, V. V., Bower, J. F., Jardim, G. A. M., da Silva, E. N. J., . . . Menna-Barreto, R. F. S. (2021). Naphthoquinones and Derivatives for Chemotherapy: Perspectives and Limitations of their Anti-trypanosomatids Activities. CURRENT PHARMACEUTICAL DESIGN, 27(15), 1807-1824. doi:10.2174/1381612826666201109111802DOI: 10.2174/1381612826666201109111802
2020
Wang, G. -W., Sokolova, O. O., Young, T. A., Christodoulou, E. M. S., Butts, C. P., & Bower, J. F. (2020). Carbonylative C-C Bond Activation of Aminocyclopropanes Using a Temporary Directing Group Strategy. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 142(45), 19006-19011. doi:10.1021/jacs.0c08973DOI: 10.1021/jacs.0c08973
Garcia-Carceles, J., Bahou, K. A., & Bower, J. F. (2020). Recent Methodologies That Exploit Oxidative Addition of C-N Bonds to Transition Metals. ACS CATALYSIS, 10(21), 12738-12759. doi:10.1021/acscatal.0c03341DOI: 10.1021/acscatal.0c03341
Wood, J. M., Satam, N. S., Almeida, R. G., Cristani, V. S., de Lima, D. P., Dantas-Pereira, L., . . . da Silva Júnior, E. N. (2020). Strategies towards potent trypanocidal drugs: Application of Rh-catalyzed [2 + 2 + 2] cycloadditions, sulfonyl phthalide annulation and nitroalkene reactions for the synthesis of substituted quinones and their evaluation against Trypanosoma cruzi. Bioorganic and Medicinal Chemistry, 28(15). doi:10.1016/j.bmc.2020.115565DOI: 10.1016/j.bmc.2020.115565
Pseudo-enantiomeric carbohydrate-based N-heterocyclic carbenes as promising chiral ligands for enantiotopic discrimination (Journal article)
Henderson, A. S., Bower, J. F., & Galan, M. C. (2020). Pseudo-enantiomeric carbohydrate-based N-heterocyclic carbenes as promising chiral ligands for enantiotopic discrimination. ORGANIC & BIOMOLECULAR CHEMISTRY, 18(16), 3012-3016. doi:10.1039/d0ob00155dDOI: 10.1039/d0ob00155d
Oxidative Addition of Alkenyl and Alkynyl Iodides to a Au<SUP>I</SUP> Complex (Journal article)
Cadge, J. A., Sparkes, H. A., Bower, J. F., & Russell, C. A. (2020). Oxidative Addition of Alkenyl and Alkynyl Iodides to a Au<SUP>I</SUP> Complex. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 59(16), 6617-6621. doi:10.1002/anie.202000473DOI: 10.1002/anie.202000473
Rhodacyclopentanones as Linchpins for the Atom Economical Assembly of Diverse Polyheterocycles (Journal article)
Wang, G. -W., Boyd, O., Young, T. A., Bertrand, S. M., & Bower, J. F. (2020). Rhodacyclopentanones as Linchpins for the Atom Economical Assembly of Diverse Polyheterocycles. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 142(4), 1740-1745. doi:10.1021/jacs.9b12421DOI: 10.1021/jacs.9b12421
Rh-Catalyzed [2+2+2] Cycloadditions with Benzoquinones: De Novo Access to Naphthoquinones for Lignan and Type II Polyketide Synthesis (Journal article)
Wood, J. M., da Silva Junior, E. N., & Bower, J. F. (2020). Rh-Catalyzed [2+2+2] Cycloadditions with Benzoquinones: De Novo Access to Naphthoquinones for Lignan and Type II Polyketide Synthesis. ORGANIC LETTERS, 22(1), 265-269. doi:10.1021/acs.orglett.9b04266DOI: 10.1021/acs.orglett.9b04266
2019
Modular Access to Eight-Membered N-Heterocycles by Directed Carbonylative C-C Bond Activation of Aminocyclopropanes (Journal article)
Boyd, O., Wang, G. -W., Sokolova, O. O., Calow, A. D. J., Bertrand, S. M., & Bower, J. F. (2019). Modular Access to Eight-Membered N-Heterocycles by Directed Carbonylative C-C Bond Activation of Aminocyclopropanes. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 58(52), 18844-18848. doi:10.1002/anie.201910276DOI: 10.1002/anie.201910276
Rhodium(I)‐Catalyzed Reductive Carbon–Carbon Bond Formation (Chapter)
Calow, A. D. J., & Bower, J. F. (2019). Rhodium(I)‐Catalyzed Reductive Carbon–Carbon Bond Formation. In Unknown Book (pp. 133-160). Wiley. doi:10.1002/9783527811908.ch7DOI: 10.1002/9783527811908.ch7
Enantioselective Aza-Heck Cyclizations of N-(Tosyloxy)carbamates: Synthesis of Pyrrolidines and Piperidines (Journal article)
Ma, X., Hazelden, I. R., Langer, T., Munday, R. H., & Bower, J. F. (2019). Enantioselective Aza-Heck Cyclizations of N-(Tosyloxy)carbamates: Synthesis of Pyrrolidines and Piperidines. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 141(8), 3356-3360. doi:10.1021/jacs.8b12689DOI: 10.1021/jacs.8b12689
Carbonylative C-C Bond Activation of Electron-Poor Cyclopropanes: Rhodium-Catalyzed (3+1+2) Cycloadditions of Cyclopropylamides (Journal article)
Dalling, A. G., Yamauchi, T., McCreanor, N. G., Cox, L., & Bower, J. F. (2019). Carbonylative C-C Bond Activation of Electron-Poor Cyclopropanes: Rhodium-Catalyzed (3+1+2) Cycloadditions of Cyclopropylamides. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 58(1), 221-225. doi:10.1002/anie.201811460DOI: 10.1002/anie.201811460
2018
Stereospecific Alkene Aziridination Using a Bifunctional Amino-Reagent: An Aza-Prilezhaev Reaction (Journal article)
Farndon, J. J., Young, T. A., & Bower, J. F. (2018). Stereospecific Alkene Aziridination Using a Bifunctional Amino-Reagent: An Aza-Prilezhaev Reaction. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 140(51), 17846-17850. doi:10.1021/jacs.8b10485DOI: 10.1021/jacs.8b10485
Iridium-Catalyzed α-Selective Arylation of Styrenes by Dual C-H Functionalization (Journal article)
Cooper, P., Crisenza, G. E. M., Feron, L. J., & Bower, J. F. (2018). Iridium-Catalyzed α-Selective Arylation of Styrenes by Dual C-H Functionalization. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 57(43), 14198-14202. doi:10.1002/anie.201808299DOI: 10.1002/anie.201808299
Synthesis of Nitrogen Heterocycles <i>via</i> Directed Carbonylative C-C Bond Activation of Cyclopropanes (Journal article)
Dalling, A. G., & Bower, J. F. (2018). Synthesis of Nitrogen Heterocycles <i>via</i> Directed Carbonylative C-C Bond Activation of Cyclopropanes. CHIMIA, 72(9), 595-600. doi:10.2533/chimia.2018.595DOI: 10.2533/chimia.2018.595
Branch-Selective and Enantioselective Iridium-Catalyzed Alkene Hydroarylation via Anilide-Directed C-H Oxidative Addition (Journal article)
Grelaud, S., Cooper, P., Feron, L. J., & Bower, J. F. (2018). Branch-Selective and Enantioselective Iridium-Catalyzed Alkene Hydroarylation via Anilide-Directed C-H Oxidative Addition. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 140(30), 9351-9356. doi:10.1021/jacs.8b04627DOI: 10.1021/jacs.8b04627
Pyrrolidines and Piperidines by Ligand-Enabled Aza-Heck Cyclizations and Cascades of <i>N</i>-(Pentafluorobenzoyloxy)carbamates (Journal article)
Hazelden, I. R., Carmona, R. C., Langer, T., Pringle, P. G., & Bower, J. F. (2018). Pyrrolidines and Piperidines by Ligand-Enabled Aza-Heck Cyclizations and Cascades of <i>N</i>-(Pentafluorobenzoyloxy)carbamates. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 57(18), 5124-5128. doi:10.1002/anie.201801109DOI: 10.1002/anie.201801109
Oxidative Addition, Transmetalation, and Reductive Elimination at a 2,2 '-Bipyridyl-Ligated Gold Center (Journal article)
Harper, M. J., Arthur, C. J., Crosby, J., Emmett, E. J., Falconer, R. L., Fensham-Smith, A. J., . . . Russell, C. A. (2018). Oxidative Addition, Transmetalation, and Reductive Elimination at a 2,2 '-Bipyridyl-Ligated Gold Center. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 140(12), 4440-4445. doi:10.1021/jacs.8b01411DOI: 10.1021/jacs.8b01411
Modular Access to Azepines by Directed Carbonylative C-C Bond Activation of Aminocyclopropanes (Journal article)
Wang, G. -W., & Bower, J. F. (2018). Modular Access to Azepines by Directed Carbonylative C-C Bond Activation of Aminocyclopropanes. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 140(8), 2743-2747. doi:10.1021/jacs.7b13087DOI: 10.1021/jacs.7b13087
2017
A Simple and Broadly Applicable C-N Bond Forming Dearomatization Protocol Enabled by Bifunctional Amino Reagents (Journal article)
Ma, X., Farndon, J. J., Young, T. A., Fey, N., & Bower, J. F. (2017). A Simple and Broadly Applicable C-N Bond Forming Dearomatization Protocol Enabled by Bifunctional Amino Reagents. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 56(46), 14531-14535. doi:10.1002/anie.201708176DOI: 10.1002/anie.201708176
A Simple and Broadly Applicable C−N Bond Forming Dearomatization Protocol Enabled by Bifunctional Amino Reagents (Journal article)
Ma, X., Farndon, J. J., Young, T. A., Fey, N., & Bower, J. F. (2017). A Simple and Broadly Applicable C−N Bond Forming Dearomatization Protocol Enabled by Bifunctional Amino Reagents. Angewandte Chemie, 129(46), 14723-14727. doi:10.1002/ange.201708176DOI: 10.1002/ange.201708176
Reductive Coupling of Acrylates with Ketones and Ketimines by a Nickel-Catalyzed Transfer-Hydrogenative Strategy (Journal article)
Buxton, C. S., Blakemore, D. C., & Bower, J. F. (2017). Reductive Coupling of Acrylates with Ketones and Ketimines by a Nickel-Catalyzed Transfer-Hydrogenative Strategy. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 56(44), 13824-13828. doi:10.1002/anie.201707531DOI: 10.1002/anie.201707531
Transition Metal Free C-N Bond Forming Dearomatizations and Aryl C-H Aminations by in Situ Release of a Hydroxylamine-Based Aminating Agent (Journal article)
Farndon, J. J., Ma, X., & Bower, J. F. (2017). Transition Metal Free C-N Bond Forming Dearomatizations and Aryl C-H Aminations by in Situ Release of a Hydroxylamine-Based Aminating Agent. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 139(40), 14005-14008. doi:10.1021/jacs.7b07830DOI: 10.1021/jacs.7b07830
Oxidative 1,2-Difunctionalization of Ethylene via Gold-Catalyzed Oxyarylation (Journal article)
Harper, M. J., Emmett, E. J., Bower, J. F., & Russell, C. A. (2017). Oxidative 1,2-Difunctionalization of Ethylene via Gold-Catalyzed Oxyarylation. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 139(36), 12386-12389. doi:10.1021/jacs.7b06668DOI: 10.1021/jacs.7b06668
Rhodium-catalyzed C-H bond activation for the synthesis of quinonoid compounds: Significant Anti-<i>Trypanosoma cruzi</i> activities and electrochemical studies of functionalized quinones (Journal article)
Jardim, G. A. M., Silva, T. L., Goulart, M. O. F., de Simone, C. A., Barbosa, J. M. C., Salomao, K., . . . da Silva Junior, E. N. (2017). Rhodium-catalyzed C-H bond activation for the synthesis of quinonoid compounds: Significant Anti-<i>Trypanosoma cruzi</i> activities and electrochemical studies of functionalized quinones. EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 136, 406-419. doi:10.1016/j.ejmech.2017.05.011DOI: 10.1016/j.ejmech.2017.05.011
Recent developments in the use of aza-Heck cyclizations for the synthesis of chiral N-heterocycles (Journal article)
Race, N. J., Hazelden, I. R., Faulkner, A., & Bower, J. F. (2017). Recent developments in the use of aza-Heck cyclizations for the synthesis of chiral N-heterocycles. CHEMICAL SCIENCE, 8(8), 5248-5260. doi:10.1039/c7sc01480eDOI: 10.1039/c7sc01480e
Recent Methodologies That Exploit C-C Single-Bond Cleavage of Strained Ring Systems by Transition Metal Complexes (Journal article)
Fumagalli, G., Stanton, S., & Bower, J. F. (2017). Recent Methodologies That Exploit C-C Single-Bond Cleavage of Strained Ring Systems by Transition Metal Complexes. CHEMICAL REVIEWS, 117(13), 9404-9432. doi:10.1021/acs.chemrev.6b00599DOI: 10.1021/acs.chemrev.6b00599
Enantioselective Narasaka-Heck cyclizations: synthesis of tetrasubstituted nitrogen-bearing stereocenters (Journal article)
Race, N. J., Faulkner, A., Fumagalli, G., Yamauchi, T., Scott, J. S., Ryden-Landergren, M., . . . Bower, J. F. (2017). Enantioselective Narasaka-Heck cyclizations: synthesis of tetrasubstituted nitrogen-bearing stereocenters. CHEMICAL SCIENCE, 8(3), 1981-1985. doi:10.1039/c6sc04466bDOI: 10.1039/c6sc04466b
2016
New Initiation Modes for Directed Carbonylative C-C Bond Activation: Rhodium-Catalyzed (3+1+2) Cycloadditions of Aminomethylcyclopropanes (Journal article)
Wang, G. -W., McCreanor, N. G., Shaw, M. H., Whittingham, W. G., & Bower, J. F. (2016). New Initiation Modes for Directed Carbonylative C-C Bond Activation: Rhodium-Catalyzed (3+1+2) Cycloadditions of Aminomethylcyclopropanes. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 138(41), 13501-13504. doi:10.1021/jacs.6b08608DOI: 10.1021/jacs.6b08608
Synthesis and applications of rhodacyclopentanones derived from C-C bond activation (Journal article)
Shaw, M. H., & Bower, J. F. (2016). Synthesis and applications of rhodacyclopentanones derived from C-C bond activation. CHEMICAL COMMUNICATIONS, 52(72), 10817-10829. doi:10.1039/c6cc04359cDOI: 10.1039/c6cc04359c
Rh-Catalyzed Reactions of 1,4-Benzoquinones with Electrophiles: C-H Iodination, Bromination, and Phenylselenation (Journal article)
Jardim, G. A. M., Bower, J. F., & da Silva Junior, E. N. (2016). Rh-Catalyzed Reactions of 1,4-Benzoquinones with Electrophiles: C-H Iodination, Bromination, and Phenylselenation. ORGANIC LETTERS, 18(18), 4454-4457. doi:10.1021/acs.orglett.6b01586DOI: 10.1021/acs.orglett.6b01586
Capture-Collapse Heterocyclization: 1,3-Diazepanes by C-N Reductive Elimination from Rhodacyclopentanones (Journal article)
McCreanor, N. G., Stanton, S., & Bower, J. F. (2016). Capture-Collapse Heterocyclization: 1,3-Diazepanes by C-N Reductive Elimination from Rhodacyclopentanones. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 138(36), 11465-11468. doi:10.1021/jacs.6b07046DOI: 10.1021/jacs.6b07046
Diverse <i>N</i>-Heterocyclic Ring Systems via Aza-Heck Cyclizations of <i>N</i>-(Pentafluorobenzoyloxy)sulfonamides (Journal article)
Hazelden, I. R., Ma, X., Langer, T., & Bower, J. F. (2016). Diverse <i>N</i>-Heterocyclic Ring Systems via Aza-Heck Cyclizations of <i>N</i>-(Pentafluorobenzoyloxy)sulfonamides. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 55(37), 11198-11202. doi:10.1002/anie.201605152DOI: 10.1002/anie.201605152
C2-Alkenylation of N-heteroaromatic compounds <i>via</i> Bronsted acid catalysis (Journal article)
Crisenza, G. E. M., Dauncey, E. M., & Bower, J. F. (2016). C2-Alkenylation of N-heteroaromatic compounds <i>via</i> Bronsted acid catalysis. ORGANIC & BIOMOLECULAR CHEMISTRY, 14(24), 5820-5825. doi:10.1039/c6ob00705hDOI: 10.1039/c6ob00705h
Directed carbonylative (3+1+2) cycloadditions of amino-substituted cyclopropanes and alkynes: reaction development and increased efficiencies using a cationic rhodium system (Journal article)
Shaw, M. H., Whittingham, W. G., & Bower, J. E. (2016). Directed carbonylative (3+1+2) cycloadditions of amino-substituted cyclopropanes and alkynes: reaction development and increased efficiencies using a cationic rhodium system. TETRAHEDRON, 72(22), 2731-2741. doi:10.1016/j.tet.2015.08.052DOI: 10.1016/j.tet.2015.08.052
Overcoming naphthoquinone deactivation: rhodium-catalyzed C-5 selective C-H iodination as a gateway to functionalized derivatives (Journal article)
Jardim, G. A. M., da Silva Junior, E. N., & Bower, J. F. (2016). Overcoming naphthoquinone deactivation: rhodium-catalyzed C-5 selective C-H iodination as a gateway to functionalized derivatives. CHEMICAL SCIENCE, 7(6), 3780-3784. doi:10.1039/c6sc00302hDOI: 10.1039/c6sc00302h
Editorial (Journal article)
Bower, J., Hansson, P., & Karton, A. (2016). Editorial. Chemical Data Collections, 2, A1-A2. doi:10.1016/j.cdc.2016.07.002DOI: 10.1016/j.cdc.2016.07.002
Carbohydrates as enantioinduction components in stereoselective catalysis (Journal article)
Henderson, A. S., Bower, J. F., & Galan, M. C. (2016). Carbohydrates as enantioinduction components in stereoselective catalysis. ORGANIC & BIOMOLECULAR CHEMISTRY, 14(17), 4008-4017. doi:10.1039/c6ob00368kDOI: 10.1039/c6ob00368k
Dichotomous mechanistic behavior in Narasaka-Heck cyclizations: electron rich Pd-catalysts generate iminyl radicals (Journal article)
Race, N. J., Faulkner, A., Shaw, M. H., & Bower, J. F. (2016). Dichotomous mechanistic behavior in Narasaka-Heck cyclizations: electron rich Pd-catalysts generate iminyl radicals. CHEMICAL SCIENCE, 7(2), 1508-1513. doi:10.1039/c5sc04037jDOI: 10.1039/c5sc04037j
Branch Selective Mural-type Alkene Hydroarylation Reactions (Journal article)
Crisenza, G. E. M., & Bower, J. F. (2016). Branch Selective Mural-type Alkene Hydroarylation Reactions. CHEMISTRY LETTERS, 45(1), 2-9. doi:10.1246/cl.150913DOI: 10.1246/cl.150913
Catalytic chirality generation: new strategies for heterocyclic chemistry (Conference Paper)
Bower, J. (2016). Catalytic chirality generation: new strategies for heterocyclic chemistry. In ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY Vol. 252. Retrieved from https://www.webofscience.com/
2015
Branch-Selective Alkene Hydroarylation by Cooperative Destabilization: Iridium-Catalyzed <i>ortho</i>-Alkylation of Acetanilides (Journal article)
Crisenza, G. E. M., Sokolova, O. O., & Bower, J. F. (2015). Branch-Selective Alkene Hydroarylation by Cooperative Destabilization: Iridium-Catalyzed <i>ortho</i>-Alkylation of Acetanilides. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 54(49), 14866-14870. doi:10.1002/anie.201506581DOI: 10.1002/anie.201506581
ChemInform Abstract: An Umpolung Approach to Alkene Carboamination: Palladium Catalyzed 1,2‐Amino‐Acylation, ‐Carboxylation, ‐Arylation, ‐Vinylation, and ‐Alkynylation. (Journal article)
Faulkner, A., Scott, J. S., & Bower, J. F. (2015). ChemInform Abstract: An Umpolung Approach to Alkene Carboamination: Palladium Catalyzed 1,2‐Amino‐Acylation, ‐Carboxylation, ‐Arylation, ‐Vinylation, and ‐Alkynylation.. ChemInform, 46(46). doi:10.1002/chin.201546136DOI: 10.1002/chin.201546136
Nucleophilic Aromatic Substitution (S<sub>N</sub>Ar) as an Approach to Challenging Carbohydrate-Aryl Ethers (Journal article)
Henderson, A. S., Medina, S., Bower, J. F., & Galan, M. C. (2015). Nucleophilic Aromatic Substitution (S<sub>N</sub>Ar) as an Approach to Challenging Carbohydrate-Aryl Ethers. ORGANIC LETTERS, 17(19), 4846-4849. doi:10.1021/acs.orglett.5b02413DOI: 10.1021/acs.orglett.5b02413
Modular Access to Substituted Azocanes via a Rhodium-Catalyzed Cycloaddition-Fragmentation Strategy (Journal article)
Shaw, M. H., Croft, R. A., Whittingham, W. G., & Bower, J. F. (2015). Modular Access to Substituted Azocanes via a Rhodium-Catalyzed Cycloaddition-Fragmentation Strategy. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 137(25), 8054-8057. doi:10.1021/jacs.5b05215DOI: 10.1021/jacs.5b05215
An Umpolung Approach to Alkene Carboamination: Palladium Catalyzed 1,2-Amino-Acylation, -Carboxylation, -Arylation, -Vinylation, and -Alkynylation (Journal article)
Faulkner, A., Scott, J. S., & Bower, J. F. (2015). An Umpolung Approach to Alkene Carboamination: Palladium Catalyzed 1,2-Amino-Acylation, -Carboxylation, -Arylation, -Vinylation, and -Alkynylation. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 137(22), 7224-7230. doi:10.1021/jacs.5b03732DOI: 10.1021/jacs.5b03732
Stereoselective synthesis of glycosides using (salen)Co catalysts as promoters (Journal article)
Medina, S., Henderson, A. S., Bower, J. F., & Galan, M. C. (2015). Stereoselective synthesis of glycosides using (salen)Co catalysts as promoters. CHEMICAL COMMUNICATIONS, 51(43), 8939-8941. doi:10.1039/c5cc02552dDOI: 10.1039/c5cc02552d
Reversible C-C Bond Activation Enables Stereocontrol in Rh-Catalyzed Carbonylative Cycloadditions of Aminocyclopropanes (Journal article)
Shaw, M. H., McCreanor, N. G., Whittingham, W. G., & Bower, J. F. (2015). Reversible C-C Bond Activation Enables Stereocontrol in Rh-Catalyzed Carbonylative Cycloadditions of Aminocyclopropanes. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 137(1), 463-468. doi:10.1021/ja511335vDOI: 10.1021/ja511335v
2014
Carbohydrate-based N-heterocyclic carbenes for enantioselective catalysis (Journal article)
Henderson, A. S., Bower, J. F., & Galan, M. C. (2014). Carbohydrate-based N-heterocyclic carbenes for enantioselective catalysis. ORGANIC & BIOMOLECULAR CHEMISTRY, 12(45), 9180-9183. doi:10.1039/c4ob02056aDOI: 10.1039/c4ob02056a
Branch-Selective, Iridium-Catalyzed Hydroarylation of Monosubstituted Alkenes via a Cooperative Destabilization Strategy (Journal article)
Crisenza, G. E. M., McCreanor, N. G., & Bower, J. F. (2014). Branch-Selective, Iridium-Catalyzed Hydroarylation of Monosubstituted Alkenes via a Cooperative Destabilization Strategy. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 136(29), 10258-10261. doi:10.1021/ja505776mDOI: 10.1021/ja505776m
Copper catalyzed Heck-like cyclizations of oxime esters (Journal article)
Faulkner, A., Race, N. J., Scott, J. S., & Bower, J. F. (2014). Copper catalyzed Heck-like cyclizations of oxime esters. CHEMICAL SCIENCE, 5(6), 2416-2421. doi:10.1039/c4sc00652fDOI: 10.1039/c4sc00652f
2013
Palladium Catalyzed Cyclizations of Oxime Esters with 1,2-Disubstituted Alkenes: Synthesis of Dihydropyrroles (Journal article)
Race, N. J., & Bower, J. F. (2013). Palladium Catalyzed Cyclizations of Oxime Esters with 1,2-Disubstituted Alkenes: Synthesis of Dihydropyrroles. ORGANIC LETTERS, 15(17), 4616-4619. doi:10.1021/ol4023112DOI: 10.1021/ol4023112
Directing Group Enhanced Carbonylative Ring Expansions of Amino-Substituted Cyclopropanes: Rhodium-Catalyzed Multicomponent Synthesis of N-Heterobicyclic Enones (Journal article)
Shaw, M. H., Melikhova, E. Y., Kloer, D. P., Whittingham, W. G., & Bower, J. F. (2013). Directing Group Enhanced Carbonylative Ring Expansions of Amino-Substituted Cyclopropanes: Rhodium-Catalyzed Multicomponent Synthesis of N-Heterobicyclic Enones. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 135(13), 4992-4995. doi:10.1021/ja401936cDOI: 10.1021/ja401936c
A Robust First-Pass Protocol for the Heck-Mizoroki Reaction (Journal article)
Murray, P. M., Bower, J. F., Cox, D. K., Galbraith, E. K., Parker, J. S., & Sweeney, J. B. (2013). A Robust First-Pass Protocol for the Heck-Mizoroki Reaction. ORGANIC PROCESS RESEARCH & DEVELOPMENT, 17(3), 397-405. doi:10.1021/op300364pDOI: 10.1021/op300364p
Palladium catalyzed cyclizations of oxime esters with 1,1-disubstituted alkenes: synthesis of α,α-disubstituted dihydropyrroles and studies towards an asymmetric protocol (Journal article)
Faulkner, A., Scott, J. S., & Bower, J. F. (2013). Palladium catalyzed cyclizations of oxime esters with 1,1-disubstituted alkenes: synthesis of α,α-disubstituted dihydropyrroles and studies towards an asymmetric protocol. CHEMICAL COMMUNICATIONS, 49(15), 1521-1523. doi:10.1039/c2cc38944dDOI: 10.1039/c2cc38944d
Catalytic chirality generation: new strategies for <i>N</i>-heterocyclic chemistry (Conference Paper)
Bower, J. F. (2013). Catalytic chirality generation: new strategies for <i>N</i>-heterocyclic chemistry. In JOURNAL OF LABELLED COMPOUNDS & RADIOPHARMACEUTICALS Vol. 56 (pp. 55). Retrieved from https://www.webofscience.com/
2012
Olefin cross-metathesis for the synthesis of heteroaromatic compounds (Journal article)
Donohoe, T. J., Bower, J. F., & Chan, L. K. M. (2012). Olefin cross-metathesis for the synthesis of heteroaromatic compounds. ORGANIC & BIOMOLECULAR CHEMISTRY, 10(7), 1322-1328. doi:10.1039/c2ob06659aDOI: 10.1039/c2ob06659a
Highly Efficient Narasaka-Heck Cyclizations Mediated by P(3,5-(CF3)2C6H3)3: Facile Access to N-Heterobicyclic Scaffolds (Journal article)
Faulkner, A., & Bower, J. F. (2012). Highly Efficient Narasaka-Heck Cyclizations Mediated by P(3,5-(CF3)2C6H3)3: Facile Access to N-Heterobicyclic Scaffolds. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 51(7), 1675-1679. doi:10.1002/anie.201107511DOI: 10.1002/anie.201107511
2011
Synthesis of 2,4,6-trisubstituted pyridines <i>via</i> an olefin cross-metathesis/Heck-cyclisation-elimination sequence (Journal article)
Donohoe, T. J., Bower, J. F., Baker, D. B., Basutto, J. A., Chan, L. K. M., & Gallagher, P. (2011). Synthesis of 2,4,6-trisubstituted pyridines <i>via</i> an olefin cross-metathesis/Heck-cyclisation-elimination sequence. CHEMICAL COMMUNICATIONS, 47(38), 10611-10613. doi:10.1039/c1cc14257gDOI: 10.1039/c1cc14257g
Heteroaromatic Synthesis <i>via</i> Olefin Cross-Metathesis: Entry to Polysubstituted Pyridines (Journal article)
Donohoe, T. J., Basutto, J. A., Bower, J. F., & Rathi, A. (2011). Heteroaromatic Synthesis <i>via</i> Olefin Cross-Metathesis: Entry to Polysubstituted Pyridines. ORGANIC LETTERS, 13(5), 1036-1039. doi:10.1021/ol103088rDOI: 10.1021/ol103088r
Formation of C-C Bonds via Iridium-Catalyzed Hydrogenation and Transfer Hydrogenation (Journal article)
Bower, J. F., & Krische, M. J. (2011). Formation of C-C Bonds via Iridium-Catalyzed Hydrogenation and Transfer Hydrogenation. IRIDIUM CATALYSIS, 34, 107-138. doi:10.1007/978-3-642-15334-1_5DOI: 10.1007/978-3-642-15334-1_5
2010
Olefin cross-metathesis-based approaches to furans: procedures for the preparation of di- and trisubstituted variants (Journal article)
Donohoe, T. J., Bower, J. F., & Basutto, J. A. (2010). Olefin cross-metathesis-based approaches to furans: procedures for the preparation of di- and trisubstituted variants. NATURE PROTOCOLS, 5(12), 2005-2010. doi:10.1038/nprot.2010.147DOI: 10.1038/nprot.2010.147
Substituted Pyrroles via Olefin Cross-Metathesis (Journal article)
Donohoe, T. J., Race, N. J., Bower, J. F., & Callens, C. K. A. (2010). Substituted Pyrroles via Olefin Cross-Metathesis. ORGANIC LETTERS, 12(18), 4094-4097. doi:10.1021/ol101681rDOI: 10.1021/ol101681r
<i>N</i>-Heterocycle construction <i>via</i> cyclic sulfamidates. Applications in synthesis (Journal article)
Bower, J. F., Rujirawanicha, J., & Gallagher, T. (2010). <i>N</i>-Heterocycle construction <i>via</i> cyclic sulfamidates. Applications in synthesis. ORGANIC & BIOMOLECULAR CHEMISTRY, 8(7), 1505-1519. doi:10.1039/b921842dDOI: 10.1039/b921842d
An expedient route to substituted furans via olefin cross-metathesis (Journal article)
Donohoe, T. J., & Bower, J. F. (2010). An expedient route to substituted furans via olefin cross-metathesis. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 107(8), 3373-3376. doi:10.1073/pnas.0913466107DOI: 10.1073/pnas.0913466107
2009
Ring-closing metathesis for the synthesis of heteroaromatics: evaluating routes to pyridines and pyridazines (Journal article)
Donohoe, T. J., Bower, J. F., Basutto, J. A., Fishlock, L. P., Procopiou, P. A., & Callens, C. K. A. (2009). Ring-closing metathesis for the synthesis of heteroaromatics: evaluating routes to pyridines and pyridazines. TETRAHEDRON, 65(44), 8969-8980. doi:10.1016/j.tet.2009.07.076DOI: 10.1016/j.tet.2009.07.076
Synthesis of substituted pyridines and pyridazines <i>via</i> ring closing metathesis (Journal article)
Donohoe, T. J., Fishlock, L. P., Basutto, J. A., Bower, J. F., Procopiou, P. A., & Thompson, A. L. (2009). Synthesis of substituted pyridines and pyridazines <i>via</i> ring closing metathesis. CHEMICAL COMMUNICATIONS, (21), 3008-3010. doi:10.1039/b904363bDOI: 10.1039/b904363b
Catalytic Carbonyl Addition through Transfer Hydrogenation: A Departure from Preformed Organometallic Reagents (Journal article)
Bower, J. F., Kim, I. S., Patman, R. L., & Krische, M. J. (2009). Catalytic Carbonyl Addition through Transfer Hydrogenation: A Departure from Preformed Organometallic Reagents. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 48(1), 34-46. doi:10.1002/anie.200802938DOI: 10.1002/anie.200802938
2008
Formation of C-C Bonds via Catalytic Hydrogenation and Transfer Hydrogenation: Vinylation, Allylation, and Enolate Addition (Journal article)
Patman, R. L., Bower, J. F., Kim, I. S., & Krische, M. J. (2008). Formation of C-C Bonds via Catalytic Hydrogenation and Transfer Hydrogenation: Vinylation, Allylation, and Enolate Addition. ALDRICHIMICA ACTA, 41(4), 95-104. Retrieved from https://www.webofscience.com/
Kepner-Tregoe Decision Analysis as a Tool To Aid Route Selection. Part 3. Application to a Back-Up Series of Compounds in the PDK Project (Journal article)
Parker, J. S., Bower, J. F., Murray, P. M., Patel, B., & Talavera, P. (2008). Kepner-Tregoe Decision Analysis as a Tool To Aid Route Selection. Part 3. Application to a Back-Up Series of Compounds in the PDK Project. ORGANIC PROCESS RESEARCH & DEVELOPMENT, 12(6), 1060-1077. doi:10.1021/op8000355DOI: 10.1021/op8000355
Diene Hydroacylation from the Alcohol or Aldehyde Oxidation Level via Ruthenium-Catalyzed C-C Bond-Forming Transfer Hydrogenation: Synthesis of β,γ-Unsaturated Ketones (Journal article)
Shibahara, F., Bower, J. F., & Krische, M. J. (2008). Diene Hydroacylation from the Alcohol or Aldehyde Oxidation Level via Ruthenium-Catalyzed C-C Bond-Forming Transfer Hydrogenation: Synthesis of β,γ-Unsaturated Ketones. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 130(43), 14120-14122. doi:10.1021/ja805356jDOI: 10.1021/ja805356j
Carbonyl propargylation from the alcohol or aldehyde oxidation level employing 1,3-enynes as surrogates to preformed allenylmetal reagents: A ruthenium-catalyzed C-C bond-forming transfer hydrogenation (Journal article)
Patman, R. L., Williams, V. M., Bower, J. F., & Krische, M. J. (2008). Carbonyl propargylation from the alcohol or aldehyde oxidation level employing 1,3-enynes as surrogates to preformed allenylmetal reagents: A ruthenium-catalyzed C-C bond-forming transfer hydrogenation. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 47(28), 5220-5223. doi:10.1002/anie.200801359DOI: 10.1002/anie.200801359
Ruthenium-catalyzed C-C bond forming transfer hydrogenation: Carbonyl allylation from the alcohol or aldehyde oxidation level employing acyclic 1,3-dienes as surrogates to preformed allyl metal reagents (Journal article)
Shibahara, F., Bower, J. F., & Krische, M. J. (2008). Ruthenium-catalyzed C-C bond forming transfer hydrogenation: Carbonyl allylation from the alcohol or aldehyde oxidation level employing acyclic 1,3-dienes as surrogates to preformed allyl metal reagents. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 130(20), 6338-+. doi:10.1021/ja801213xDOI: 10.1021/ja801213x
Iridium-catalyzed C-C coupling via transfer hydrogenation: Carbonyl addition from the alcohol or aldehyde oxidation level employing 1,3-cyclohexadiene (Journal article)
Bower, J. F., Patman, R. L., & Krische, M. J. (2008). Iridium-catalyzed C-C coupling via transfer hydrogenation: Carbonyl addition from the alcohol or aldehyde oxidation level employing 1,3-cyclohexadiene. ORGANIC LETTERS, 10(5), 1033-1035. doi:10.1021/ol800159wDOI: 10.1021/ol800159w
2007
Catalytic C-C coupling via transfer hydrogenation: Reverse prenylation, crotylation, and allylation from the alcohol or aldehyde oxidation level (Journal article)
Bower, J. F., Skucas, E., Patman, R. L., & Krische, M. J. (2007). Catalytic C-C coupling via transfer hydrogenation: Reverse prenylation, crotylation, and allylation from the alcohol or aldehyde oxidation level. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 129(49), 15134-+. doi:10.1021/ja077389bDOI: 10.1021/ja077389b
Cyclic sulfamidates as precursors to alkylidene pyrrolidines and piperidines (Journal article)
Bower, J. F., Szeto, P., & Gallagher, T. (2007). Cyclic sulfamidates as precursors to alkylidene pyrrolidines and piperidines. ORGANIC LETTERS, 9(23), 4909-4912. doi:10.1021/ol7022104DOI: 10.1021/ol7022104
Carbonyl allylation in the absence of preformed allyl metal reagents: Reverse Prenylation via iridium-catalyzed hydrogenative coupling of dimethylallene (Journal article)
Skucas, E., Bower, J. F., & Krische, M. J. (2007). Carbonyl allylation in the absence of preformed allyl metal reagents: Reverse Prenylation via iridium-catalyzed hydrogenative coupling of dimethylallene. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 129(42), 12678-+. doi:10.1021/ja075971uDOI: 10.1021/ja075971u
Reactivity of cyclic sulfamidates towards phosphonate-stabilised enolates:: synthesis and applications of α-phosphono lactams (Journal article)
Bower, J. F., Williams, A. J., Woodward, H. L., Szeto, P., Lawrence, R. M., & Gallagher, T. (2007). Reactivity of cyclic sulfamidates towards phosphonate-stabilised enolates:: synthesis and applications of α-phosphono lactams. ORGANIC & BIOMOLECULAR CHEMISTRY, 5(16), 2636-2644. doi:10.1039/b706315fDOI: 10.1039/b706315f
Enantiopure 1,4-benzoxazines via 1,2-cyclic sulfamidates. Synthesis of levofloxacin (Journal article)
Bower, J. F., Szeto, P., & Gallagher, T. (2007). Enantiopure 1,4-benzoxazines via 1,2-cyclic sulfamidates. Synthesis of levofloxacin. ORGANIC LETTERS, 9(17), 3283-3286. doi:10.1021/ol0712475DOI: 10.1021/ol0712475
Stereospecific construction of substituted piperidines. Synthesis of (-)-paroxetine and (+)-laccarin (Journal article)
Bower, J. F., Riis-Johannessen, T., Szeto, P., Whitehead, A. J., & Gallagher, T. (2007). Stereospecific construction of substituted piperidines. Synthesis of (-)-paroxetine and (+)-laccarin. CHEMICAL COMMUNICATIONS, (7), 728-730. doi:10.1039/b617260aDOI: 10.1039/b617260a
Cyclic sulfamidates as versatile lactam precursors. An evaluation of synthetic strategies towards (-)-aphanorphine (Journal article)
Bower, J. F., Szeto, P., & Gallagher, T. (2007). Cyclic sulfamidates as versatile lactam precursors. An evaluation of synthetic strategies towards (-)-aphanorphine. ORGANIC & BIOMOLECULAR CHEMISTRY, 5(1), 143-150. doi:10.1039/b614999eDOI: 10.1039/b614999e
2006
Reactivity of cyclic sulfamidates towards sulfur-stabilised enolates. Stereocontrolled synthesis of functionalised lactams (Journal article)
Bower, J. F., Chakthong, S., Svenda, J., Williams, A. J., Lawrence, R. M., Szeto, P., & Gallagher, T. (2006). Reactivity of cyclic sulfamidates towards sulfur-stabilised enolates. Stereocontrolled synthesis of functionalised lactams. ORGANIC & BIOMOLECULAR CHEMISTRY, 4(10), 1868-1877. doi:10.1039/b601804aDOI: 10.1039/b601804a
2005
Cyclic sulfamidates as lactam precursors. An efficient asymmetric synthesis of (-)-aphanorphine (Journal article)
Bower, J. F., Szeto, P., & Gallagher, T. (2005). Cyclic sulfamidates as lactam precursors. An efficient asymmetric synthesis of (-)-aphanorphine. CHEMICAL COMMUNICATIONS, (46), 5793-5795. doi:10.1039/b510761jDOI: 10.1039/b510761j
2004
Cyclic sulfamidates as vehicles for the synthesis of substituted lactams (Journal article)
Bower, J. F., Svenda, J., Williams, A. J., Charmant, J. P. H., Lawrence, R. M., Szeto, P., & Gallagher, T. (2004). Cyclic sulfamidates as vehicles for the synthesis of substituted lactams. ORGANIC LETTERS, 6(25), 4727-4730. doi:10.1021/ol048036+DOI: 10.1021/ol048036+
2003
Praseodymium complexes of 2,2′-bipyridine;: the crystal and molecular structures of Pr(bipy)<sub>3</sub>(NCS)<sub>3</sub>, Pr(bipy)<sub>2</sub>(NO<sub>3</sub>)<sub>3</sub>, Pr(bipy)<sub>2</sub>Cl<sub>3</sub>(OH<sub>2</sub>)•EtOH and Pr(bipy)(S<sub>2</sub>CNEt<sub>2</sub>)<sub>3</sub> (Journal article)
Bower, J. F., Cotton, S. A., Fawcett, J., Hughes, R. S., & Russell, D. R. (2003). Praseodymium complexes of 2,2′-bipyridine;: the crystal and molecular structures of Pr(bipy)<sub>3</sub>(NCS)<sub>3</sub>, Pr(bipy)<sub>2</sub>(NO<sub>3</sub>)<sub>3</sub>, Pr(bipy)<sub>2</sub>Cl<sub>3</sub>(OH<sub>2</sub>)•EtOH and Pr(bipy)(S<sub>2</sub>CNEt<sub>2</sub>)<sub>3</sub>. POLYHEDRON, 22(2), 347-354. doi:10.1016/S0277-5387(02)01359-1DOI: 10.1016/S0277-5387(02)01359-1
