| Year |
Citation |
Score |
| 2024 |
de Carvalho R, Wood J, Almeida R, Berry N, da Silva Júnior E, Bower J. The Synthesis and Reactivity of Naphthoquinonynes. Angewandte Chemie (International Ed. in English). e202400188. PMID 38445547 DOI: 10.1002/anie.202400188 |
0.332 |
|
| 2023 |
Jing C, Mao W, Bower JF. Iridium-Catalyzed Enantioselective Alkene Hydroalkylation via a Heteroaryl-Directed Enolization-Decarboxylation Sequence. Journal of the American Chemical Society. 145: 23918-23924. PMID 37879082 DOI: 10.1021/jacs.3c10163 |
0.377 |
|
| 2023 |
Smith MJS, Tu W, Robertson CM, Bower JF. Stereospecific Aminative Cyclizations Triggered by Intermolecular Aza-Prilezhaev Alkene Aziridination. Angewandte Chemie (International Ed. in English). e202312797. PMID 37846756 DOI: 10.1002/anie.202312797 |
0.34 |
|
| 2023 |
Zhu Y, Smith MJS, Tu W, Bower JF. A Stereospecific Alkene 1,2-Aminofunctionalization Platform for the Assembly of Complex Nitrogen-Containing Ring Systems. Angewandte Chemie (International Ed. in English). e202301262. PMID 36812298 DOI: 10.1002/anie.202301262 |
0.343 |
|
| 2022 |
Cooper P, Dalling AG, Farrar EHE, Aldhous TP, Grélaud S, Lester E, Feron LJ, Kemmitt PD, Grayson MN, Bower JF. Atom and step economical synthesis of acyclic quaternary centers iridium-catalyzed hydroarylative cross-coupling of 1,1-disubstituted alkenes. Chemical Science. 13: 11183-11189. PMID 36320466 DOI: 10.1039/d2sc02790a |
0.318 |
|
| 2022 |
Cadge JA, Gates PJ, Bower JF, Russell CA. Migratory Insertion of CO into a Au-C Bond. Journal of the American Chemical Society. 144: 19719-19725. PMID 36282061 DOI: 10.1021/jacs.2c10432 |
0.315 |
|
| 2022 |
Jing C, Jones BT, Adams RJ, Bower JF. Cyclopropane-Fused -Heterocycles via Aza-Heck-Triggered C(sp)-H Functionalization Cascades. Journal of the American Chemical Society. PMID 36083505 DOI: 10.1021/jacs.2c08304 |
0.337 |
|
| 2022 |
Calow ADJ, Dailler D, Bower JF. Carbonylative N-Heterocyclization via Nitrogen-Directed C-C Bond Activation of Nonactivated Cyclopropanes. Journal of the American Chemical Society. PMID 35715228 DOI: 10.1021/jacs.2c02921 |
0.379 |
|
| 2022 |
Sokolova OO, Bower J. An endo-Directing-Group Strategy Unlocks Enantioselective (3+1+2) Carbonylative Cycloadditions of Aminocyclopropanes. Angewandte Chemie (International Ed. in English). PMID 35611866 DOI: 10.1002/anie.202205007 |
0.379 |
|
| 2021 |
Jones BT, García-Cárceles J, Caiger L, Hazelden IR, Lewis RJ, Langer T, Bower JF. Complex Polyheterocycles and the Stereochemical Reassignment of Pileamartine A via Aza-Heck Triggered Aryl C-H Functionalization Cascades. Journal of the American Chemical Society. PMID 34546043 DOI: 10.1021/jacs.1c08615 |
0.373 |
|
| 2021 |
Jing C, Farndon JJ, Bower JF. Dearomatizing Amination Reactions. Chemical Record (New York, N.Y.). PMID 34240537 DOI: 10.1002/tcr.202100104 |
0.37 |
|
| 2021 |
O'Neil LG, Bower JF. Electrophilic Aminating Agents in Total Synthesis. Angewandte Chemie (International Ed. in English). PMID 33942955 DOI: 10.1002/anie.202102864 |
0.308 |
|
| 2020 |
Wang GW, Sokolova OO, Young TA, Christodoulou EMS, Butts CP, Bower JF. Carbonylative C-C Bond Activation of Aminocyclopropanes Using a Temporary Directing Group Strategy. Journal of the American Chemical Society. PMID 33125219 DOI: 10.1021/jacs.0c08973 |
0.317 |
|
| 2020 |
Wood JM, Satam NS, Almeida RG, Cristani VS, de Lima DP, Dantas-Pereira L, Salomão K, Menna-Barreto RFS, Namboothiri INN, Bower JF, da Silva Júnior EN. 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 & Medicinal Chemistry. 28: 115565. PMID 32631558 DOI: 10.1016/J.Bmc.2020.115565 |
0.388 |
|
| 2020 |
Sokolova OO, Bower JF. Selective Carbon-Carbon Bond Cleavage of Cyclopropylamine Derivatives. Chemical Reviews. PMID 32567848 DOI: 10.1021/Acs.Chemrev.0C00166 |
0.463 |
|
| 2020 |
Henderson AS, Bower JF, Galan MC. Pseudo-enantiomeric carbohydrate-based N-heterocyclic carbenes as promising chiral ligands for enantiotopic discrimination. Organic & Biomolecular Chemistry. PMID 32267909 DOI: 10.1039/D0Ob00155D |
0.459 |
|
| 2020 |
Wang GW, Boyd O, Young TA, Bertrand SM, Bower JF. Rhodacyclopentanones as Linchpins for the Atom Economical Assembly of Diverse Polyheterocycles. Journal of the American Chemical Society. PMID 31961154 DOI: 10.1021/Jacs.9B12421 |
0.33 |
|
| 2020 |
Russell CA, Bower J, Cadge J, Sparkes H. Oxidative addition of alkenyl and alkynyl iodides to a Au(I) complex. Angewandte Chemie (International Ed. in English). PMID 31951062 DOI: 10.1002/Anie.202000473 |
0.361 |
|
| 2019 |
Wood JM, da Silva Júnior EN, Bower JF. Rh-Catalyzed [2 + 2 + 2] Cycloadditions with Benzoquinones: De Novo Access to Naphthoquinones for Lignan and Type II Polyketide Synthesis. Organic Letters. PMID 31850764 DOI: 10.1021/Acs.Orglett.9B04266 |
0.382 |
|
| 2019 |
Boyd O, Wang G, Sokolova O, Calow A, Bertrand S, Bower J. Modular Access to Eight-Membered N-Heterocycles by Directed Carbonylative C-C Bond Activation of Aminocyclopropanes. Angewandte Chemie (International Ed. in English). PMID 31585028 DOI: 10.1002/Anie.201910276 |
0.456 |
|
| 2019 |
Ma X, Hazelden IR, Langer T, Munday RH, Bower JF. Enantioselective Aza-Heck Cyclizations of N-(Tosyloxy)carbamates: Synthesis of Pyrrolidines and Piperidines. Journal of the American Chemical Society. PMID 30775918 DOI: 10.1021/Jacs.8B12689 |
0.398 |
|
| 2018 |
Farndon JJ, Young TA, Bower JF. Stereospecific Alkene Aziridination Using a Bifunctional Amino-Reagent: An Aza-Prilezhaev Reaction. Journal of the American Chemical Society. PMID 30543287 DOI: 10.1021/Jacs.8B10485 |
0.368 |
|
| 2018 |
Dalling AG, Yamauchi T, McCreanor NG, Cox L, Bower J. Carbonylative C-C Bond Activation of Electron-Poor Cyclopropanes: Rhodium-Catalyzed (3+1+2) Cycloadditions of Cyclopropylamides. Angewandte Chemie (International Ed. in English). PMID 30397992 DOI: 10.1002/Anie.201811460 |
0.454 |
|
| 2018 |
Dalling AG, Bower JF. Synthesis of Nitrogen Heterocycles Directed Carbonylative C-C Bond Activation of Cyclopropanes. Chimia. 72: 595-600. PMID 30257733 DOI: 10.2533/Chimia.2018.595 |
0.486 |
|
| 2018 |
Cooper P, Crisenza G, Feron L, Bower J. Iridium-Catalyzed α-Selective Arylation of Styrenes by Dual C-H Functionalization. Angewandte Chemie (International Ed. in English). PMID 30171652 DOI: 10.1002/Anie.201808299 |
0.782 |
|
| 2018 |
Grélaud S, Cooper P, Feron LJ, Bower JF. Branch-Selective and Enantioselective Iridium-Catalyzed Alkene Hydroarylation via Anilide-Directed C-H Oxidative Addition. Journal of the American Chemical Society. PMID 30024748 DOI: 10.1021/Jacs.8B04627 |
0.52 |
|
| 2018 |
Harper MJ, Arthur CJ, Crosby J, Emmett EJ, Falconer RL, Fensham-Smith AJ, Gates PJ, Leman T, McGrady JE, Bower JF, Russell CA. Oxidative Addition, Transmetalation, and Reductive Elimination at a 2,2'-Bipyridyl-Ligated Gold Center. Journal of the American Chemical Society. PMID 29553258 DOI: 10.1021/Jacs.8B01411 |
0.421 |
|
| 2018 |
Hazelden IR, Carmona RC, Langer T, Pringle PG, Bower JF. Pyrrolidines and Piperidines by Ligand-Enabled Aza-Heck Cyclizations and Cascades of N-(Pentafluorobenzoyloxy)carbamates. Angewandte Chemie (International Ed. in English). PMID 29488677 DOI: 10.1002/Anie.201801109 |
0.379 |
|
| 2018 |
Wang GW, Bower JF. Modular Access to Azepines by Directed Carbonylative C-C Bond Activation of Aminocyclopropanes. Journal of the American Chemical Society. PMID 29461050 DOI: 10.1021/Jacs.7B13087 |
0.473 |
|
| 2017 |
Race NJ, Hazelden IR, Faulkner A, Bower JF. Recent developments in the use of aza-Heck cyclizations for the synthesis of chiral N-heterocycles. Chemical Science. 8: 5248-5260. PMID 28959424 DOI: 10.1039/C7Sc01480E |
0.432 |
|
| 2017 |
Farndon JJ, Ma X, Bower JF. 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. PMID 28953364 DOI: 10.1021/Jacs.7B07830 |
0.452 |
|
| 2017 |
Ma X, Farndon J, Young T, Fey N, Bower J. A Simple and Broadly Applicable C-N Bond Forming Dearomatization Protocol Enabled by Bifunctional Amino-Reagents. Angewandte Chemie (International Ed. in English). PMID 28925055 DOI: 10.1002/Anie.201708176 |
0.47 |
|
| 2017 |
Buxton CS, Blakemore DC, Bower JF. Reductive Coupling of Acrylates with Ketones and Ketimines by a Nickel-Catalyzed Transfer-Hydrogenative Strategy. Angewandte Chemie (International Ed. in English). PMID 28868751 DOI: 10.1002/Anie.201707531 |
0.508 |
|
| 2017 |
Harper MJ, Emmett EJ, Bower JF, Russell CA. Oxidative 1,2-Difunctionalization of Ethylene via Gold-Catalyzed Oxyarylation. Journal of the American Chemical Society. PMID 28829593 DOI: 10.1021/Jacs.7B06668 |
0.371 |
|
| 2017 |
Jardim GAM, Silva TL, Goulart MOF, de Simone CA, Barbosa JMC, Salomão K, de Castro SL, Bower JF, da Silva Júnior EN. Rhodium-catalyzed C-H bond activation for the synthesis of quinonoid compounds: Significant Anti-Trypanosoma cruzi activities and electrochemical studies of functionalized quinones. European Journal of Medicinal Chemistry. 136: 406-419. PMID 28521262 DOI: 10.1016/J.Ejmech.2017.05.011 |
0.427 |
|
| 2017 |
Race NJ, Faulkner A, Fumagalli G, Yamauchi T, Scott JS, Rydén-Landergren M, Sparkes HA, Bower JF. Enantioselective Narasaka-Heck cyclizations: synthesis of tetrasubstituted nitrogen-bearing stereocenters. Chemical Science. 8: 1981-1985. PMID 28451314 DOI: 10.1039/C6Sc04466B |
0.448 |
|
| 2017 |
Fumagalli G, Stanton S, Bower JF. Recent Methodologies That Exploit C-C Single-Bond Cleavage of Strained Ring Systems by Transition Metal Complexes. Chemical Reviews. PMID 28075115 DOI: 10.1021/Acs.Chemrev.6B00599 |
0.415 |
|
| 2017 |
Race NJ, Faulkner A, Fumagalli G, Yamauchi T, Scott JS, Rydén-Landergren M, Sparkes HA, Bower JF. Enantioselective Narasaka–Heck Cyclization Synfacts. 13: 182-182. DOI: 10.1055/S-0036-1589900 |
0.444 |
|
| 2017 |
Buxton C, Blakemore D, Bower J. Reductive Coupling of Acrylates with Ketones and Ketimines via a Nickel‐Catalyzed Transfer Hydrogenative Reductant Relay Strategy Angewandte Chemie. DOI: 10.1002/Ange.201707531 |
0.498 |
|
| 2016 |
Jardim GAM, da Silva Júnior EN, Bower JF. Overcoming naphthoquinone deactivation: rhodium-catalyzed C-5 selective C-H iodination as a gateway to functionalized derivatives. Chemical Science. 7: 3780-3784. PMID 30155019 DOI: 10.1039/C6Sc00302H |
0.477 |
|
| 2016 |
Race NJ, Faulkner A, Shaw MH, Bower JF. Dichotomous mechanistic behavior in Narasaka-Heck cyclizations: electron rich Pd-catalysts generate iminyl radicals. Chemical Science. 7: 1508-1513. PMID 29899895 DOI: 10.1039/C5Sc04037J |
0.41 |
|
| 2016 |
Wang GW, McCreanor NG, Shaw MH, Whittingham WG, Bower JF. New Initiation Modes for Directed Carbonylative C-C Bond Activation: Rhodium-Catalyzed (3 + 1 + 2) Cycloadditions of Aminomethylcyclopropanes. Journal of the American Chemical Society. PMID 27709913 DOI: 10.1021/Jacs.6B08608 |
0.434 |
|
| 2016 |
Jardim GA, Bower JF, da Silva Júnior EN. Rh-Catalyzed Reactions of 1,4-Benzoquinones with Electrophiles: C-H Iodination, Bromination, and Phenylselenation. Organic Letters. 18: 4454-7. PMID 27599589 DOI: 10.1021/Acs.Orglett.6B01586 |
0.793 |
|
| 2016 |
McCreanor NG, Stanton S, Bower JF. Capture-Collapse Heterocyclization: 1,3-Diazepanes by C-N Reductive Elimination from Rhodacyclopentanones. Journal of the American Chemical Society. 138: 11465-8. PMID 27589060 DOI: 10.1021/Jacs.6B07046 |
0.4 |
|
| 2016 |
Hazelden IR, Ma X, Langer T, Bower JF. Diverse N-Heterocyclic Ring Systems via Aza-Heck Cyclizations of N-(Pentafluorobenzoyloxy)sulfonamides. Angewandte Chemie (International Ed. in English). PMID 27460965 DOI: 10.1002/Anie.201605152 |
0.388 |
|
| 2016 |
Shaw MH, Bower JF. Synthesis and applications of rhodacyclopentanones derived from C-C bond activation. Chemical Communications (Cambridge, England). PMID 27385089 DOI: 10.1039/C6Cc04359C |
0.441 |
|
| 2016 |
Crisenza GE, Dauncey EM, Bower JF. C2-Alkenylation of N-heteroaromatic compounds via Brønsted acid catalysis. Organic & Biomolecular Chemistry. 14: 5820-5. PMID 27138371 DOI: 10.1039/C6Ob00705H |
0.782 |
|
| 2016 |
Henderson AS, Bower JF, Galan MC. Carbohydrates as enantioinduction components in stereoselective catalysis. Organic & Biomolecular Chemistry. PMID 27064817 DOI: 10.1039/C6Ob00368K |
0.38 |
|
| 2016 |
Crisenza GEM, Bower JF. Branch selective Murai-type alkene hydroarylation reactions Chemistry Letters. 45: 2-9. DOI: 10.1246/Cl.150913 |
0.412 |
|
| 2016 |
Shaw MH, Whittingham WG, Bower JF. Directed carbonylative (3+1+2) cycloadditions of amino-substituted cyclopropanes and alkynes: Reaction development and increased efficiencies using a cationic rhodium system Tetrahedron. 72: 2731-2741. DOI: 10.1016/J.Tet.2015.08.052 |
0.51 |
|
| 2015 |
Crisenza GE, Sokolova OO, Bower JF. Branch-Selective Alkene Hydroarylation by Cooperative Destabilization: Iridium-Catalyzed ortho-Alkylation of Acetanilides. Angewandte Chemie (International Ed. in English). PMID 26490739 DOI: 10.1002/Anie.201506581 |
0.78 |
|
| 2015 |
Henderson AS, Medina S, Bower JF, Galan MC. Nucleophilic Aromatic Substitution (SNAr) as an Approach to Challenging Carbohydrate-Aryl Ethers. Organic Letters. PMID 26379123 DOI: 10.1021/Acs.Orglett.5B02413 |
0.499 |
|
| 2015 |
Shaw MH, Croft RA, Whittingham WG, Bower JF. Modular Access to Substituted Azocanes via a Rhodium-Catalyzed Cycloaddition-Fragmentation Strategy. Journal of the American Chemical Society. 137: 8054-7. PMID 26090897 DOI: 10.1021/Jacs.5B05215 |
0.45 |
|
| 2015 |
Faulkner A, Scott JS, Bower JF. An Umpolung Approach to Alkene Carboamination: Palladium Catalyzed 1,2-Amino-Acylation, -Carboxylation, -Arylation, -Vinylation, and -Alkynylation. Journal of the American Chemical Society. 137: 7224-30. PMID 26020544 DOI: 10.1021/Jacs.5B03732 |
0.434 |
|
| 2015 |
Medina S, Henderson AS, Bower JF, Galan MC. Stereoselective synthesis of glycosides using (salen)Co catalysts as promoters. Chemical Communications (Cambridge, England). 51: 8939-41. PMID 25925803 DOI: 10.1039/C5Cc02552D |
0.377 |
|
| 2015 |
Shaw MH, McCreanor NG, Whittingham WG, Bower JF. Reversible C-C bond activation enables stereocontrol in Rh-catalyzed carbonylative cycloadditions of aminocyclopropanes. Journal of the American Chemical Society. 137: 463-8. PMID 25539136 DOI: 10.1021/Ja511335V |
0.53 |
|
| 2014 |
Henderson AS, Bower JF, Galan MC. Carbohydrate-based N-heterocyclic carbenes for enantioselective catalysis. Organic & Biomolecular Chemistry. 12: 9180-3. PMID 25296562 DOI: 10.1039/C4Ob02056A |
0.504 |
|
| 2014 |
Crisenza GE, McCreanor NG, Bower JF. Branch-selective, iridium-catalyzed hydroarylation of monosubstituted alkenes via a cooperative destabilization strategy. Journal of the American Chemical Society. 136: 10258-61. PMID 25019322 DOI: 10.1021/Ja505776M |
0.77 |
|
| 2014 |
Faulkner A, Race NJ, Scott JS, Bower JF. Copper catalyzed Heck-like cyclizations of oxime esters Chemical Science. 5: 2416-2421. DOI: 10.1039/C4Sc00652F |
0.44 |
|
| 2013 |
Race NJ, Bower JF. Palladium catalyzed cyclizations of oxime esters with 1,2-disubstituted alkenes: synthesis of dihydropyrroles. Organic Letters. 15: 4616-9. PMID 23981032 DOI: 10.1021/Ol4023112 |
0.466 |
|
| 2013 |
Shaw MH, Melikhova EY, Kloer DP, Whittingham WG, Bower JF. 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: 4992-5. PMID 23488745 DOI: 10.1021/Ja401936C |
0.442 |
|
| 2013 |
Faulkner A, Scott JS, Bower JF. 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 (Cambridge, England). 49: 1521-3. PMID 23321771 DOI: 10.1039/C2Cc38944D |
0.45 |
|
| 2013 |
Murray PM, Bower JF, Cox DK, Galbraith EK, Parker JS, Sweeney JB. A robust first-pass protocol for the heck-mizoroki reaction Organic Process Research and Development. 17: 397-405. DOI: 10.1021/Op300364P |
0.432 |
|
| 2012 |
Donohoe TJ, Bower JF, Chan LK. Olefin cross-metathesis for the synthesis of heteroaromatic compounds. Organic & Biomolecular Chemistry. 10: 1322-8. PMID 22215025 DOI: 10.1039/C2Ob06659A |
0.61 |
|
| 2011 |
Donohoe TJ, Bower JF, Baker DB, Basutto JA, Chan LK, Gallagher P. Synthesis of 2,4,6-trisubstituted pyridines via an olefin cross-metathesis/Heck-cyclisation-elimination sequence. Chemical Communications (Cambridge, England). 47: 10611-3. PMID 21870019 DOI: 10.1039/C1Cc14257G |
0.632 |
|
| 2011 |
Bower JF, Krische MJ. Formation of C-C Bonds via Iridium-Catalyzed Hydrogenation and Transfer Hydrogenation. Topics in Organometallic Chemistry. 34: 107-138. PMID 21822399 DOI: 10.1007/978-3-642-15334-1_5 |
0.631 |
|
| 2011 |
Donohoe TJ, Basutto JA, Bower JF, Rathi A. Heteroaromatic synthesis via olefin cross-metathesis: entry to polysubstituted pyridines. Organic Letters. 13: 1036-9. PMID 21268598 DOI: 10.1021/Ol103088R |
0.639 |
|
| 2010 |
Donohoe TJ, Bower JF, Basutto JA. Olefin cross-metathesis-based approaches to furans: procedures for the preparation of di- and trisubstituted variants. Nature Protocols. 5: 2005-10. PMID 21127493 DOI: 10.1038/Nprot.2010.147 |
0.636 |
|
| 2010 |
Donohoe TJ, Race NJ, Bower JF, Callens CK. Substituted pyrroles via olefin cross-metathesis. Organic Letters. 12: 4094-7. PMID 20712303 DOI: 10.1021/Ol101681R |
0.587 |
|
| 2010 |
Bower JF, Rujirawanich J, Gallagher T. N-heterocycle construction via cyclic sulfamidates. Applications in synthesis. Organic & Biomolecular Chemistry. 8: 1505-19. PMID 20237659 DOI: 10.1039/B921842D |
0.675 |
|
| 2010 |
Donohoe TJ, Bower JF. An expedient route to substituted furans via olefin cross-metathesis. Proceedings of the National Academy of Sciences of the United States of America. 107: 3373-6. PMID 20142508 DOI: 10.1073/Pnas.0913466107 |
0.634 |
|
| 2009 |
Donohoe TJ, Fishlock LP, Basutto JA, Bower JF, Procopiou PA, Thompson AL. Synthesis of substituted pyridines and pyridazines via ring closing metathesis. Chemical Communications (Cambridge, England). 3008-10. PMID 19462069 DOI: 10.1039/B904363B |
0.617 |
|
| 2009 |
Bower JF, Kim IS, Patman RL, Krische MJ. Catalytic carbonyl addition through transfer hydrogenation: a departure from preformed organometallic reagents. Angewandte Chemie (International Ed. in English). 48: 34-46. PMID 19040235 DOI: 10.1002/Anie.200802938 |
0.798 |
|
| 2009 |
Donohoe TJ, Bower JF, Basutto JA, Fishlock LP, Procopiou PA, Callens CKA. Ring-closing metathesis for the synthesis of heteroaromatics: evaluating routes to pyridines and pyridazines Tetrahedron. 65: 8969-8980. DOI: 10.1016/J.Tet.2009.07.076 |
0.617 |
|
| 2008 |
Patman RL, Bower JF, Kim IS, Krische MJ. Formation of C-C Bonds via Catalytic Hydrogenation and Transfer Hydrogenation: Vinylation, Allylation, and Enolate Addition of Carbonyl Compounds and Imines. Aldrichimica Acta. 41: 95-104. PMID 22403445 DOI: 10.1002/9781118354520.ch16 |
0.792 |
|
| 2008 |
Shibahara F, Bower JF, Krische MJ. Diene hydroacylation from the alcohol or aldehyde oxidation level via ruthenium-catalyzed C-C bond-forming transfer hydrogenation: synthesis of beta,gamma-unsaturated ketones. Journal of the American Chemical Society. 130: 14120-2. PMID 18841895 DOI: 10.1021/Ja805356J |
0.6 |
|
| 2008 |
Patman RL, Williams VM, Bower JF, Krische MJ. 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 Ed. in English). 47: 5220-3. PMID 18528831 DOI: 10.1002/Anie.200801359 |
0.816 |
|
| 2008 |
Shibahara F, Bower JF, Krische MJ. 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: 6338-9. PMID 18444617 DOI: 10.1021/Ja801213X |
0.629 |
|
| 2008 |
Bower JF, Patman RL, Krische MJ. Iridium-catalyzed C-C coupling via transfer hydrogenation: carbonyl addition from the alcohol or aldehyde oxidation level employing 1,3-cyclohexadiene. Organic Letters. 10: 1033-5. PMID 18254642 DOI: 10.1021/Ol800159W |
0.807 |
|
| 2008 |
Shibahara F, Bower JF, Krische MJ. Ru-Catalyzed Carbonyl Allylations from Alcohols or Aldehydes Synfacts. 2008: 831-831. DOI: 10.1055/S-2008-1077906 |
0.57 |
|
| 2008 |
Bower JF, Patman RL, Krische MJ. Iridium-Promoted C-C Coupling through Transfer Hydrogenation Synfacts. 2008: 505-505. DOI: 10.1055/S-2008-1072635 |
0.59 |
|
| 2008 |
Bower JF, Skucas E, Patman RL, Krische MJ. Reverse Prenylation, Crotylation and Allylation of Alcohols and Aldehydes via Transfer Hydrogenation Synfacts. 2008: 293-293. DOI: 10.1055/S-2008-1042740 |
0.558 |
|
| 2008 |
Bower J, Kim I, Patman R, Krische M. Katalytische Carbonyladdition durch Transferhydrierung: weg von vorab gebildeten Organometallreagentien Angewandte Chemie. 121: 36-48. DOI: 10.1002/Ange.200802938 |
0.772 |
|
| 2007 |
Bower JF, Skucas E, Patman RL, Krische MJ. 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: 15134-5. PMID 18020342 DOI: 10.1021/Ja077389B |
0.786 |
|
| 2007 |
Bower JF, Williams AJ, Woodward HL, Szeto P, Lawrence RM, Gallagher T. Reactivity of cyclic sulfamidates towards phosphonate-stabilised enolates: synthesis and applications of alpha-phosphono lactams. Organic & Biomolecular Chemistry. 5: 2636-44. PMID 18019539 DOI: 10.1039/B706315F |
0.676 |
|
| 2007 |
Bower JF, Szeto P, Gallagher T. Cyclic sulfamidates as precursors to alkylidene pyrrolidines and piperidines. Organic Letters. 9: 4909-12. PMID 17949100 DOI: 10.1021/Ol7022104 |
0.625 |
|
| 2007 |
Skucas E, Bower JF, Krische MJ. 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: 12678-9. PMID 17900123 DOI: 10.1021/Ja075971U |
0.62 |
|
| 2007 |
Bower JF, Szeto P, Gallagher T. Enantiopure 1,4-benzoxazines via 1,2-cyclic sulfamidates. Synthesis of levofloxacin. Organic Letters. 9: 3283-6. PMID 17661473 DOI: 10.1021/Ol0712475 |
0.635 |
|
| 2007 |
Bower JF, Riis-Johannessen T, Szeto P, Whitehead AJ, Gallagher T. Stereospecific construction of substituted piperidines. Synthesis of (-)-paroxetine and (+)-laccarin. Chemical Communications (Cambridge, England). 728-30. PMID 17392964 DOI: 10.1039/B617260A |
0.682 |
|
| 2007 |
Bower JF, Szeto P, Gallagher T. Cyclic sulfamidates as versatile lactam precursors. An evaluation of synthetic strategies towards (-)-aphanorphine. Organic & Biomolecular Chemistry. 5: 143-50. PMID 17164919 DOI: 10.1039/B614999E |
0.684 |
|
| 2007 |
Bower JF, Riis-Johannessen T, Szeto P, Whitehead AJ, Gallagher T. Synthesis of (-)-Paroxetine and (+)-Laccarin Synfacts. 2007: 574-574. DOI: 10.1055/S-2007-968516 |
0.606 |
|
| 2006 |
Bower JF, Chakthong S, Svenda J, Williams AJ, Lawrence RM, Szeto P, Gallagher T. Reactivity of cyclic sulfamidates towards sulfur-stabilised enolates. Stereocontrolled synthesis of functionalised lactams. Organic & Biomolecular Chemistry. 4: 1868-77. PMID 16688332 DOI: 10.1039/B601804A |
0.577 |
|
| 2005 |
Bower JF, Szeto P, Gallagher T. Cyclic sulfamidates as lactam precursors. An efficient asymmetric synthesis of (-)-aphanorphine. Chemical Communications (Cambridge, England). 5793-5. PMID 16307148 DOI: 10.1039/B510761J |
0.627 |
|
| 2004 |
Bower JF, Svenda J, Williams AJ, Charmant JP, Lawrence RM, Szeto P, Gallagher T. Cyclic sulfamidates as vehicles for the synthesis of substituted lactams. Organic Letters. 6: 4727-30. PMID 15575671 DOI: 10.1021/Ol048036+ |
0.634 |
|
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