Year |
Citation |
Score |
2024 |
Alexander BW, Bartfield NM, Gupta V, Mercado BQ, Del Campo M, Herzon SB. An oxidative photocyclization approach to the synthesis of alkaloids. Science (New York, N.Y.). 383: 849-854. PMID 38386756 DOI: 10.1126/science.adl6163 |
0.313 |
|
2023 |
DiBello M, Healy AR, Nikolayevskiy H, Xu Z, Herzon SB. Structure Elucidation of Secondary Metabolites: Current Frontiers and Lingering Pitfalls. Accounts of Chemical Research. PMID 37220079 DOI: 10.1021/acs.accounts.3c00183 |
0.796 |
|
2023 |
Hsu IT, Herzon SB. Fragment Coupling Approach to Diaporthein B. The Journal of Organic Chemistry. 88: 2221-2244. PMID 36737056 DOI: 10.1021/acs.joc.2c02655 |
0.304 |
|
2022 |
Goethe O, DiBello M, Herzon SB. Total synthesis of structurally diverse pleuromutilin antibiotics. Nature Chemistry. PMID 36163267 DOI: 10.1038/s41557-022-01027-7 |
0.329 |
|
2021 |
Tomanik M, Xu Z, Guo F, Wang Z, Yang KR, Batista VS, Herzon SB. Development of an Enantioselective Synthesis of (-)-Euonyminol. The Journal of Organic Chemistry. PMID 34784213 DOI: 10.1021/acs.joc.1c02167 |
0.312 |
|
2021 |
Wernke KM, Tirla A, Xue M, Surovtseva YV, Menges FS, Herzon SB. Probing Microbiome Genotoxicity: A Stable Colibactin Provides Insight into Structure-Activity Relationships and Facilitates Mechanism of Action Studies. Journal of the American Chemical Society. PMID 34524796 DOI: 10.1021/jacs.1c07559 |
0.787 |
|
2021 |
Tirla A, Wernke KM, Herzon SB. On the Stability and Spectroscopic Properties of 5-Hydroxyoxazole-4-carboxylic Acid Derivatives. Organic Letters. PMID 34180681 DOI: 10.1021/acs.orglett.1c01796 |
0.762 |
|
2021 |
Hsu IT, Tomanik M, Herzon SB. Metric-Based Analysis of Convergence in Complex Molecule Synthesis. Accounts of Chemical Research. PMID 33523640 DOI: 10.1021/acs.accounts.0c00817 |
0.332 |
|
2020 |
Williams PC, Wernke KM, Tirla A, Herzon SB. Employing chemical synthesis to study the structure and function of colibactin, a "dark matter" metabolite. Natural Product Reports. PMID 33174565 DOI: 10.1039/d0np00072h |
0.787 |
|
2020 |
Tomanik M, Economou C, Frischling MC, Xue M, Marks VA, Mercado BQ, Herzon SB. Development of a Convergent Enantioselective Synthetic Route to (-)-Myrocin G. The Journal of Organic Chemistry. PMID 32615040 DOI: 10.1021/Acs.Joc.0C00891 |
0.414 |
|
2020 |
Wernke KM, Xue M, Tirla A, Kim CS, Crawford JM, Herzon SB. Structure and bioactivity of colibactin. Bioorganic & Medicinal Chemistry Letters. 30: 127280. PMID 32527463 DOI: 10.1016/J.Bmcl.2020.127280 |
0.794 |
|
2020 |
Xue M, Wernke K, Herzon SB. Depurination of colibactin-derived interstrand cross-links. Biochemistry. PMID 31977191 DOI: 10.1021/acs.biochem.9b01070 |
0.787 |
|
2020 |
Rose JA, Mahapatra S, Li X, Wang C, Chen L, Swick SM, Herzon SB. Synthesis of the bis(cyclohexenone) core of (−)-lomaiviticin A Chemical Science. 11: 7462-7467. DOI: 10.1039/D0Sc02770G |
0.432 |
|
2019 |
Tomanik M, Herzon SB, Hsu IT. Fragment coupling reactions in total synthesis that form carbon-carbon bonds via carbanionic or free radical intermediates. Angewandte Chemie (International Ed. in English). PMID 31869476 DOI: 10.1002/Anie.201913645 |
0.314 |
|
2019 |
Healy AR, Wernke KM, Kim CS, Lees NR, Crawford JM, Herzon SB. Addendum: Synthesis and reactivity of precolibactin 886. Nature Chemistry. PMID 31719668 DOI: 10.1038/S41557-019-0383-X |
0.762 |
|
2019 |
Healy AR, Wernke KM, Kim CS, Lees NR, Crawford JM, Herzon SB. Synthesis and reactivity of precolibactin 886. Nature Chemistry. 11: 890-898. PMID 31548676 DOI: 10.1038/S41557-019-0338-2 |
0.808 |
|
2019 |
Xue M, Kim CS, Healy AR, Wernke KM, Wang Z, Frischling MC, Shine EE, Wang W, Herzon SB, Crawford JM. Structure elucidation of colibactin and its DNA cross-links. Science (New York, N.Y.). PMID 31395743 DOI: 10.1126/Science.Aax2685 |
0.798 |
|
2019 |
Hoang KM, Lees NR, Herzon SB. Programmable Synthesis of 2-Deoxyglycosides. Journal of the American Chemical Society. PMID 31059254 DOI: 10.1021/Jacs.9B03982 |
0.367 |
|
2018 |
Economou C, Romaire JP, Scott TZ, Parr BT, Herzon SB. A convergent approach to batzelladine alkaloids. Total syntheses of (+)-batzelladine E, (-)-dehydrobatzelladine C, and (+)-batzelladine K. Tetrahedron. 74: 3188-3197. PMID 33911315 DOI: 10.1016/j.tet.2018.04.050 |
0.642 |
|
2018 |
Economou C, Tomanik M, Herzon SB. Synthesis of Myrocin G, the Putative Active Form of the Myrocin Antitumor Antibiotics. Journal of the American Chemical Society. PMID 30415540 DOI: 10.1021/Jacs.8B10891 |
0.463 |
|
2018 |
Shine EE, Xue M, Patel JR, Healy AR, Surovtseva YV, Herzon SB, Crawford JM. Model colibactins exhibit human cell genotoxicity in the absence of host bacteria. Acs Chemical Biology. PMID 30403848 DOI: 10.1021/Acschembio.8B00714 |
0.612 |
|
2018 |
Xue M, Shine EE, Wang W, Crawford JM, Herzon SB. Characterization of natural colibactin-nucleobase adducts by tandem MS and isotopic labeling. Support for DNA alkylation by cyclopropane ring opening. Biochemistry. PMID 30365310 DOI: 10.1021/Acs.Biochem.8B01023 |
0.413 |
|
2018 |
Ma X, Herzon SB. Cobalt bis(acetylacetonate)--butyl hydroperoxide-triethylsilane: a general reagent combination for the Markovnikov-selective hydrofunctionalization of alkenes by hydrogen atom transfer. Beilstein Journal of Organic Chemistry. 14: 2259-2265. PMID 30202480 DOI: 10.3762/Bjoc.14.201 |
0.761 |
|
2018 |
Goethe O, Heuer A, Ma X, Wang Z, Herzon SB. Antibacterial properties and clinical potential of pleuromutilins. Natural Product Reports. PMID 29979463 DOI: 10.1039/C8Np00042E |
0.751 |
|
2018 |
Ma X, Kucera R, Goethe OF, Murphy SK, Herzon SB. Directed C-H bond oxidation of (+)-pleuromutilin. The Journal of Organic Chemistry. PMID 29664634 DOI: 10.1021/Acs.Joc.8B00462 |
0.787 |
|
2018 |
Herzon S. Emergent Properties of Natural Products Synlett. 29: 1823-1835. DOI: 10.1055/S-0037-1610242 |
0.366 |
|
2018 |
Economou C, Romaire JP, Scott TZ, Parr BT, Herzon SB. A convergent approach to batzelladine alkaloids. Total syntheses of (+)-batzelladine E, (−)-dehydrobatzelladine C, and (+)-batzelladine K Tetrahedron. 74: 3188-3197. DOI: 10.1016/J.Tet.2018.04.050 |
0.669 |
|
2017 |
Tripathi P, Shine EE, Healy AR, Kim CS, Herzon SB, Bruner SD, Crawford JM. ClbS is a cyclopropane hydrolase that confers colibactin resistance. Journal of the American Chemical Society. PMID 29112397 DOI: 10.1021/Jacs.7B09971 |
0.629 |
|
2017 |
Zeng M, Murphy SK, Herzon SB. Development of a modular synthetic route to (+)-pleuromutilin, (+)- 12-epi-mutilins, and related structures. Journal of the American Chemical Society. PMID 29048164 DOI: 10.1021/Jacs.7B09869 |
0.572 |
|
2017 |
Nikolayevskiy H, Moe Tun MK, Rablen PR, Ben Mamoun C, Herzon SB. A complex stereochemical relay approach to the antimalarial alkaloid ocimicide A1. Evidence for a structural revision. Chemical Science. 8: 4867-4871. PMID 28959410 DOI: 10.1039/C7Sc01127J |
0.789 |
|
2017 |
Herzon SB. The Mechanism of Action of (-)-Lomaiviticin A. Accounts of Chemical Research. PMID 28956437 DOI: 10.1021/Acs.Accounts.7B00347 |
0.385 |
|
2017 |
Herzon SB, Vanderwal CD. Introduction: Natural Product Synthesis. Chemical Reviews. 117: 11649-11650. PMID 28950704 DOI: 10.1021/Acs.Chemrev.7B00520 |
0.379 |
|
2017 |
Healy AR, Herzon SB. Molecular basis of gut microbiome-associated colorectal cancer: A synthetic perspective. Journal of the American Chemical Society. PMID 28949546 DOI: 10.1021/Jacs.7B07807 |
0.649 |
|
2017 |
Murphy SK, Zeng M, Herzon SB. Scalable Synthesis of a Key Intermediate for the Production of Pleuromutilin-Based Antibiotics. Organic Letters. PMID 28858512 DOI: 10.1021/Acs.Orglett.7B02476 |
0.554 |
|
2017 |
Guntaka NS, Healy AR, Crawford JM, Herzon SB, Bruner SD. Structure and Functional Analysis of ClbQ, an Unusual Intermediate-Releasing Thioesterase from the Colibactin Biosynthetic Pathway. Acs Chemical Biology. PMID 28846367 DOI: 10.1021/Acschembio.7B00479 |
0.634 |
|
2017 |
Murphy SK, Zeng M, Herzon SB. A modular and enantioselective synthesis of the pleuromutilin antibiotics. Science (New York, N.Y.). 356: 956-959. PMID 28572392 DOI: 10.1126/Science.Aan0003 |
0.571 |
|
2017 |
Ma X, Dang H, Rose JA, Rablen PR, Herzon SB. Hydroheteroarylation of unactivated alkenes using N-methoxyheteroarenium salts. Journal of the American Chemical Society. PMID 28359149 DOI: 10.1021/Jacs.7B02388 |
0.765 |
|
2017 |
Trautman E, Healy AR, Shine E, Herzon SB, Crawford JM. Domain-targeted metabolomics delineates the heterocycle assembly steps of colibactin biosynthesis. Journal of the American Chemical Society. PMID 28240912 DOI: 10.1021/Jacs.7B00659 |
0.589 |
|
2016 |
Xue M, Herzon SB. Mechanism of Nucleophilic Activation of (-)-Lomaiviticin A. Journal of the American Chemical Society. 138: 15559-15562. PMID 27934014 DOI: 10.1021/Jacs.6B09657 |
0.357 |
|
2016 |
Healy AR, Nikolayevskiy H, Patel JR, Crawford JM, Herzon SB. A Mechanistic Model for Colibactin-Induced Genotoxicity. Journal of the American Chemical Society. 138: 15563-15570. PMID 27934011 DOI: 10.1021/Jacs.6B10354 |
0.804 |
|
2016 |
Murphy SK, Zeng M, Herzon SB. Stereoselective Multicomponent Reactions Using Zincate Nucleophiles: β-Dicarbonyl Synthesis and Functionalization. Organic Letters. PMID 27670226 DOI: 10.1021/Acs.Orglett.6B02320 |
0.545 |
|
2016 |
Ma X, Herzon SB. Synthesis of Ketones and Esters from Heteroatom-Functionalized Alkenes by Cobalt-Mediated Hydrogen Atom Transfer. The Journal of Organic Chemistry. PMID 27598718 DOI: 10.1021/Acs.Joc.6B01709 |
0.766 |
|
2016 |
Ma X, Herzon SB. Intermolecular hydropyridylation of unactivated alkenes. Journal of the American Chemical Society. PMID 27384921 DOI: 10.1021/Jacs.6B05271 |
0.747 |
|
2016 |
Colis LC, Herzon SB. Synergistic potentiation of (-)-lomaiviticin A cytotoxicity by the ATR inhibitor VE-821. Bioorganic & Medicinal Chemistry Letters. PMID 27177826 DOI: 10.1016/J.Bmcl.2016.04.090 |
0.325 |
|
2016 |
Healy AR, Vizcaino MI, Crawford JM, Herzon SB. A convergent and modular synthesis of candidate precolibactins. Structural revision of precolibactin A. Journal of the American Chemical Society. PMID 27025153 DOI: 10.1021/Jacs.6B02276 |
0.672 |
|
2016 |
Woo CM, Li Z, Paulson EK, Herzon SB. Structural basis for DNA cleavage by the potent antiproliferative agent (-)-lomaiviticin A. Proceedings of the National Academy of Sciences of the United States of America. PMID 26929332 DOI: 10.1073/Pnas.1519846113 |
0.673 |
|
2016 |
Surovtseva YV, Jairam V, Salem AF, Sundaram RK, Bindra RS, Herzon SB. Characterization of cardiac glycoside natural products as potent inhibitors of DNA double-strand break repair by a whole cell double immunofluorescence assay. Journal of the American Chemical Society. PMID 26927829 DOI: 10.1021/Jacs.6B00162 |
0.341 |
|
2016 |
Surovtseva Y, Jairam V, Sundaram R, Bindra R, Herzon S. Abstract 2174: A high-throughput, high-content assay for the discovery of new inhibitors of DNA double-strand break repair Cancer Research. 76: 2174-2174. DOI: 10.1158/1538-7445.Am2016-2174 |
0.338 |
|
2015 |
Ma X, Herzon SB. Non-classical selectivities in the reduction of alkenes by cobalt-mediated hydrogen atom transfer. Chemical Science. 6: 6250-6255. PMID 30090243 DOI: 10.1039/C5Sc02476E |
0.741 |
|
2015 |
Parr BT, Economou C, Herzon SB. A concise synthesis of (+)-batzelladine B from simple pyrrole-based starting materials. Nature. 525: 507-10. PMID 26375010 DOI: 10.1038/Nature14902 |
0.708 |
|
2015 |
Zeng M, Herzon SB. Synthesis of 1,3-Amino Alcohols, 1,3-Diols, Amines, and Carboxylic Acids from Terminal Alkynes. The Journal of Organic Chemistry. 80: 8604-18. PMID 26203776 DOI: 10.1021/Acs.Joc.5B01220 |
0.35 |
|
2015 |
Colis LC, Hegan DC, Kaneko M, Glazer PM, Herzon SB. Mechanism of action studies of lomaiviticin a and the monomeric lomaiviticin aglycon. Selective and potent activity toward DNA double-strand break repair-deficient cell lines. Journal of the American Chemical Society. 137: 5741-7. PMID 25849366 DOI: 10.1021/Ja513117P |
0.326 |
|
2015 |
Kats-Kagan R, Herzon SB. The discovery of a novel route to highly substituted α-tropolones enables expedient entry to the core of the gukulenins. Organic Letters. 17: 2030-3. PMID 25839211 DOI: 10.1021/Acs.Orglett.5B00841 |
0.371 |
|
2014 |
King SM, Herzon SB. The Hasubanan and Acutumine Alkaloids. The Alkaloids. Chemistry and Biology. 73: 161-222. PMID 26521650 DOI: 10.1016/B978-0-12-411565-1.00003-2 |
0.573 |
|
2014 |
King SM, Herzon SB. Substrate-modified functional group reactivity: hasubanan and acutumine alkaloid syntheses. The Journal of Organic Chemistry. 79: 8937-47. PMID 25135456 DOI: 10.1021/Jo501516X |
0.576 |
|
2014 |
Woo CM, Ranjan N, Arya DP, Herzon SB. Analysis of diazofluorene DNA binding and damaging activity: DNA cleavage by a synthetic monomeric diazofluorene. Angewandte Chemie (International Ed. in English). 53: 9325-8. PMID 25044348 DOI: 10.1002/Anie.201404137 |
0.67 |
|
2014 |
Colis LC, Woo CM, Hegan DC, Li Z, Glazer PM, Herzon SB. The cytotoxicity of (-)-lomaiviticin A arises from induction of double-strand breaks in DNA. Nature Chemistry. 6: 504-10. PMID 24848236 DOI: 10.1038/Nchem.1944 |
0.679 |
|
2014 |
King SM, Ma X, Herzon SB. A method for the selective hydrogenation of alkenyl halides to alkyl halides. Journal of the American Chemical Society. 136: 6884-7. PMID 24824195 DOI: 10.1021/Ja502885C |
0.768 |
|
2014 |
Kaneko M, Herzon SB. Scope and limitations of 2-deoxy- and 2,6-dideoxyglycosyl bromides as donors for the synthesis of β-2-deoxy- and β-2,6-dideoxyglycosides. Organic Letters. 16: 2776-9. PMID 24786757 DOI: 10.1021/Ol501101F |
0.349 |
|
2014 |
Zeng M, Li L, Herzon SB. A highly active and air-stable ruthenium complex for the ambient temperature anti-Markovnikov reductive hydration of terminal alkynes. Journal of the American Chemical Society. 136: 7058-67. PMID 24786693 DOI: 10.1021/Ja501738A |
0.371 |
|
2014 |
Li L, Herzon SB. Temporal separation of catalytic activities allows anti-Markovnikov reductive functionalization of terminal alkynes. Nature Chemistry. 6: 22-7. PMID 24345942 DOI: 10.1038/Nchem.1799 |
0.338 |
|
2014 |
King SM, Herzon SB. The Hasubanan and Acutumine Alkaloids Alkaloids: Chemistry and Biology. 73: 161-222. DOI: 10.1016/B978-0-12-411565-1.00003-2 |
0.526 |
|
2013 |
Calandra NA, King SM, Herzon SB. Development of enantioselective synthetic routes to the hasubanan and acutumine alkaloids. The Journal of Organic Chemistry. 78: 10031-57. PMID 24032758 DOI: 10.1021/Jo401889B |
0.61 |
|
2013 |
Woo CM, Gholap SL, Herzon SB. Insights into lomaiviticin biosynthesis. Isolation and structure elucidation of (-)-homoseongomycin. Journal of Natural Products. 76: 1238-41. PMID 23803003 DOI: 10.1021/Np400355H |
0.802 |
|
2013 |
Zheng J, Urkalan KB, Herzon SB. Direct synthesis of β-N-glycosides by the reductive glycosylation of azides with protected and native carbohydrate donors. Angewandte Chemie (International Ed. in English). 52: 6068-71. PMID 23609997 DOI: 10.1002/Anie.201301264 |
0.343 |
|
2013 |
King SM, Calandra NA, Herzon SB. Total syntheses of (-)-acutumine and (-)-dechloroacutumine. Angewandte Chemie (International Ed. in English). 52: 3642-5. PMID 23427090 DOI: 10.1002/Anie.201210076 |
0.564 |
|
2013 |
Mitcheltree MJ, Konst ZA, Herzon SB. A practical method for regiocontrolled one-carbon ring contraction Tetrahedron. 69: 5634-5639. DOI: 10.1016/J.Tet.2013.04.027 |
0.322 |
|
2012 |
Woo CM, Gholap SL, Lu L, Kaneko M, Li Z, Ravikumar PC, Herzon SB. Development of enantioselective synthetic routes to (-)-kinamycin F and (-)-lomaiviticin aglycon. Journal of the American Chemical Society. 134: 17262-73. PMID 23030272 DOI: 10.1021/Ja307497H |
0.794 |
|
2012 |
Woo CM, Beizer NE, Janso JE, Herzon SB. Isolation of lomaiviticins C-E, transformation of lomaiviticin C to lomaiviticin A, complete structure elucidation of lomaiviticin A, and structure-activity analyses. Journal of the American Chemical Society. 134: 15285-8. PMID 22963534 DOI: 10.1021/Ja3074984 |
0.643 |
|
2012 |
Bloomfield AJ, Herzon SB. Room temperature, palladium-mediated P-arylation of secondary phosphine oxides. Organic Letters. 14: 4370-3. PMID 22905711 DOI: 10.1021/Ol301831K |
0.318 |
|
2012 |
Herzon SB, Woo CM. The diazofluorene antitumor antibiotics: structural elucidation, biosynthetic, synthetic, and chemical biological studies. Natural Product Reports. 29: 87-118. PMID 22037715 DOI: 10.1039/C1Np00052G |
0.705 |
|
2012 |
Mulcahy SP, Woo CM, Ding W, Ellestad GA, Herzon SB. Characterization of a reductively-activated elimination pathway relevant to the biological chemistry of the kinamycins and lomaiviticins Chemical Science. 3: 1070-1074. DOI: 10.1039/C2Sc00854H |
0.691 |
|
2011 |
Herzon SB, Calandra NA, King SM. Efficient entry to the hasubanan alkaloids: first enantioselective total syntheses of (-)-hasubanonine, (-)-runanine, (-)-delavayine, and (+)-periglaucine B. Angewandte Chemie (International Ed. in English). 50: 8863-6. PMID 21638524 DOI: 10.1002/Anie.201102226 |
0.56 |
|
2011 |
Herzon SB, Lu L, Woo CM, Gholap SL. 11-Step enantioselective synthesis of (-)-lomaiviticin aglycon. Journal of the American Chemical Society. 133: 7260-3. PMID 21280607 DOI: 10.1021/Ja200034B |
0.811 |
|
2011 |
Tun MKM, Wüstmann DJ, Herzon SB. A robust and scalable synthesis of the potent neuroprotective agent (-)-huperzine A Chemical Science. 2: 2251-2253. DOI: 10.1039/C1Sc00455G |
0.325 |
|
2011 |
Herzon SB, Calandra NA, King SM. Cover Picture: Efficient Entry to the Hasubanan Alkaloids: First Enantioselective Total Syntheses of (−)-Hasubanonine, (−)-Runanine, (−)-Delavayine, and (+)-Periglaucine B (Angew. Chem. Int. Ed. 38/2011) Angewandte Chemie International Edition. 50: 8761-8761. DOI: 10.1002/Anie.201105017 |
0.54 |
|
2011 |
Herzon SB, Calandra NA, King SM. Titelbild: Efficient Entry to the Hasubanan Alkaloids: First Enantioselective Total Syntheses of (−)-Hasubanonine, (−)-Runanine, (−)-Delavayine, and (+)-Periglaucine B (Angew. Chem. 38/2011) Angewandte Chemie. 123: 8919-8919. DOI: 10.1002/Ange.201105017 |
0.54 |
|
2010 |
Woo CM, Lu L, Gholap SL, Smith DR, Herzon SB. Development of a convergent entry to the diazofluorene antitumor antibiotics: enantioselective synthesis of kinamycin F. Journal of the American Chemical Society. 132: 2540-1. PMID 20141138 DOI: 10.1021/Ja910769J |
0.805 |
|
2010 |
Bloomfield AJ, Qian JM, Herzon SB. Single-step synthesis of secondary phosphine oxides Organometallics. 29: 4193-4195. DOI: 10.1021/Om100571W |
0.391 |
|
2009 |
Gholap SL, Woo CM, Ravikumar PC, Herzon SB. Synthesis of the fully glycosylated cyclohexenone core of lomaiviticin A. Organic Letters. 11: 4322-5. PMID 19719089 DOI: 10.1021/Ol901710B |
0.781 |
|
2008 |
Herzon SB, Hartwig JF. Hydroaminoalkylation of unactivated olefins with dialkylamines. Journal of the American Chemical Society. 130: 14940-1. PMID 18937477 DOI: 10.1021/Ja806367E |
0.521 |
|
2007 |
Herzon SB, Hartwig JF. Direct, catalytic hydroaminoalkylation of unactivated olefins with N-alkyl arylamines. Journal of the American Chemical Society. 129: 6690-1. PMID 17474747 DOI: 10.1021/Ja0718366 |
0.529 |
|
2007 |
Wulff JE, Herzon SB, Siegrist R, Myers AG. Evidence for the rapid conversion of stephacidin B into the electrophilic monomer avrainvillamide in cell culture. Journal of the American Chemical Society. 129: 4898-9. PMID 17397160 DOI: 10.1021/Ja0690971 |
0.706 |
|
2005 |
Herzon SB, Myers AG. Enantioselective synthesis of stephacidin B. Journal of the American Chemical Society. 127: 5342-4. PMID 15826171 DOI: 10.1021/Ja0510616 |
0.608 |
|
2003 |
Myers AG, Herzon SB. Identification of a novel Michael acceptor group for the reversible addition of oxygen- and sulfur-based nucleophiles. Synthesis and reactivity of the 3-alkylidene-3H-indole 1-oxide function of avrainvillamide. Journal of the American Chemical Society. 125: 12080-1. PMID 14518979 DOI: 10.1021/Ja0372006 |
0.544 |
|
2003 |
Krow GR, Lin G, Herzon SB, Thomas AM, Moore KP, Huang Q, Carroll PJ. Convenient preparations of 2,4-methanopyrrolidine and 5-carboxy-2,4-methanopyrrolidines. The Journal of Organic Chemistry. 68: 7562-4. PMID 12968923 DOI: 10.1021/Jo0348672 |
0.312 |
|
2003 |
Krow GR, Lin G, Rapolu D, Fang Y, Lester WS, Herzon SB, Sonnet PE. The rearrangement route to 2-azabicyclo[2.1.1]hexanes. Solvent and electrophile control of neighboring group participation. The Journal of Organic Chemistry. 68: 5292-9. PMID 12816491 DOI: 10.1021/Jo034394Z |
0.3 |
|
2002 |
Krow GR, Herzon SB, Lin G, Qiu F, Sonnet PE. Complex-induced proximity effects. Temperature-dependent regiochemical diversity in lithiation-electrophilic substitution reactions of N-BOC-2-azabicyclo[2.1.1]hexane. 2,4- and 3,5-methanoprolines. Organic Letters. 4: 3151-4. PMID 12201739 DOI: 10.1021/Ol026509B |
0.337 |
|
2001 |
Krow GR, Lester WS, Liu N, Yuan J, Hiller A, Duo J, Herzon SB, Nguyen Y, Cannon K. Synthesis of novel 2-azabicyclo[2.2.0]- and [2.1.1]hexanols. The Journal of Organic Chemistry. 66: 1811-7. PMID 11262132 DOI: 10.1021/Jo001558S |
0.315 |
|
2001 |
Krow GR, Lee YB, Lester WS, Liu N, Yuan J, Duo J, Herzon SB, Nguyen Y, Zacharias D. 2-Azabicyclo[2.1.1]hexanes. 2. Substitutent effects on the bromine-mediated rearrangement of 2-azabicyclo[2.2.0]hex-5-enes. The Journal of Organic Chemistry. 66: 1805-10. PMID 11262131 DOI: 10.1021/Jo0015570 |
0.357 |
|
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