Year |
Citation |
Score |
2016 |
Bagdanoff JT, Behenna DC, Stockdill JL, Stoltz BM. Enantioselective Synthesis of Caprolactam and Enone Precursors to the Heterocyclic DEFG Ring System of Zoanthenol. European Journal of Organic Chemistry. 2016: 2101-2104. PMID 28090188 DOI: 10.1002/Ejoc.201600223 |
0.797 |
|
2015 |
Craig RA, Loskot SA, Mohr JT, Behenna DC, Harned AM, Stoltz BM. Palladium-Catalyzed Enantioselective Decarboxylative Allylic Alkylation of Cyclopentanones. Organic Letters. 17: 5160-3. PMID 26501770 DOI: 10.1021/Acs.Orglett.5B02376 |
0.808 |
|
2015 |
Korch KM, Eidamshaus C, Behenna DC, Nam S, Horne D, Stoltz BM. Enantioselective synthesis of α-secondary and α-tertiary piperazin-2-ones and piperazines by catalytic asymmetric allylic alkylation. Angewandte Chemie (International Ed. in English). 54: 179-83. PMID 25382664 DOI: 10.1002/Anie.201408609 |
0.782 |
|
2014 |
Liu Y, Liniger M, McFadden RM, Roizen JL, Malette J, Reeves CM, Behenna DC, Seto M, Kim J, Mohr JT, Virgil SC, Stoltz BM. Formal total syntheses of classic natural product target molecules via palladium-catalyzed enantioselective alkylation. Beilstein Journal of Organic Chemistry. 10: 2501-12. PMID 25383121 DOI: 10.3762/Bjoc.10.261 |
0.804 |
|
2014 |
Reeves CM, Behenna DC, Stoltz BM. Development of (trimethylsilyl)ethyl ester protected enolates and applications in palladium-catalyzed enantioselective allylic alkylation: intermolecular cross-coupling of functionalized electrophiles. Organic Letters. 16: 2314-7. PMID 24724872 DOI: 10.1021/Ol500355Z |
0.763 |
|
2014 |
Krishnan S, Shanmuganathan MV, Behenna D, Stoltz BM, Prasadarao NV. Angiotensin II receptor type 1--a novel target for preventing neonatal meningitis in mice by Escherichia coli K1. The Journal of Infectious Diseases. 209: 409-19. PMID 24041786 DOI: 10.1093/Infdis/Jit499 |
0.631 |
|
2013 |
Bennett NB, Duquette DC, Kim J, Liu WB, Marziale AN, Behenna DC, Virgil SC, Stoltz BM. Expanding insight into asymmetric palladium-catalyzed allylic alkylation of N-heterocyclic molecules and cyclic ketones. Chemistry (Weinheim An Der Bergstrasse, Germany). 19: 4414-8. PMID 23447555 DOI: 10.1002/Chem.201300030 |
0.819 |
|
2013 |
Behenna DC, Stoltz BM. Natural products as inspiration for reaction development: Catalytic enantioselective decarboxylative reactions of prochiral enolate equivalents Topics in Organometallic Chemistry. 44: 281-313. DOI: 10.1007/3418-2012-49 |
0.749 |
|
2012 |
Keith JA, Behenna DC, Sherden N, Mohr JT, Ma S, Marinescu SC, Nielsen RJ, Oxgaard J, Stoltz BM, Goddard WA. The reaction mechanism of the enantioselective Tsuji allylation: inner-sphere and outer-sphere pathways, internal rearrangements, and asymmetric C-C bond formation. Journal of the American Chemical Society. 134: 19050-60. PMID 23102088 DOI: 10.1021/Ja306860N |
0.773 |
|
2012 |
Behenna DC, Liu Y, Yurino T, Kim J, White DE, Virgil SC, Stoltz BM. Enantioselective construction of quaternary N-heterocycles by palladium-catalysed decarboxylative allylic alkylation of lactams. Nature Chemistry. 4: 130-3. PMID 22270628 DOI: 10.1038/Nchem.1222 |
0.775 |
|
2011 |
Behenna DC, Mohr JT, Sherden NH, Marinescu SC, Harned AM, Tani K, Seto M, Ma S, Novák Z, Krout MR, McFadden RM, Roizen JL, Enquist JA, White DE, Levine SR, et al. Enantioselective decarboxylative alkylation reactions: catalyst development, substrate scope, and mechanistic studies. Chemistry (Weinheim An Der Bergstrasse, Germany). 17: 14199-223. PMID 22083969 DOI: 10.1002/Chem.201003383 |
0.711 |
|
2011 |
Behenna DC, Krishnan S, Stoltz BM. Confirmation of the absolute configuration of (-)-aurantioclavine Tetrahedron Letters. 52: 2152-2154. DOI: 10.1016/J.Tetlet.2010.11.074 |
0.705 |
|
2009 |
Sherden NH, Behenna DC, Virgil SC, Stoltz BM. Unusual allylpalladium carboxylate complexes: identification of the resting state of catalytic enantioselective decarboxylative allylic alkylation reactions of ketones. Angewandte Chemie (International Ed. in English). 48: 6840-3. PMID 19672907 DOI: 10.1002/Anie.200902575 |
0.805 |
|
2009 |
Stockdill JL, Behenna DC, Stoltz BM. Unexpected decarbonylation during an acid-mediated cyclization to access the carbocyclic core of zoanthenol Tetrahedron Letters. 50: 3182-3184. DOI: 10.1016/J.Tetlet.2009.01.121 |
0.807 |
|
2009 |
Stockdill JL, Behenna DC, McClory A, Stoltz BM. An efficient synthesis of the carbocyclic core of zoanthenol Tetrahedron. 65: 6571-6575. DOI: 10.1016/J.Tet.2009.05.023 |
0.809 |
|
2008 |
Behenna DC, Corey EJ. Simple enantioselective approach to synthetic limonoids. Journal of the American Chemical Society. 130: 6720-1. PMID 18444655 DOI: 10.1021/Ja802376G |
0.554 |
|
2008 |
Behenna DC, Stockdill JL, Stoltz BM. The biology and chemistry of the zoanthamine alkaloids. Angewandte Chemie (International Ed. in English). 47: 2365-86. PMID 18307180 DOI: 10.1002/Anie.200703172 |
0.757 |
|
2008 |
Behenna D, Stockdill J, Stoltz B. Biologie und Chemie der Zoanthamin-Alkaloide Angewandte Chemie. 120: 2400-2421. DOI: 10.1002/Ange.200703172 |
0.734 |
|
2007 |
Keith JA, Behenna DC, Mohr JT, Ma S, Marinescu SC, Oxgaard J, Stoltz BM, Goddard WA. The inner-sphere process in the enantioselective Tsuji allylation reaction with (S)-t-Bu-phosphinooxazoline ligands. Journal of the American Chemical Society. 129: 11876-7. PMID 17824701 DOI: 10.1021/Ja070516J |
0.805 |
|
2007 |
Tani K, Behenna DC, McFadden RM, Stoltz BM. A facile and modular synthesis of phosphinooxazoline ligands. Organic Letters. 9: 2529-31. PMID 17536810 DOI: 10.1021/Ol070884S |
0.726 |
|
2007 |
Behenna DC, Stockdill JL, Stoltz BM. Synthesis of the carbocyclic core of zoanthenol: implementation of an unusual acid-catalyzed cyclization. Angewandte Chemie (International Ed. in English). 46: 4077-80. PMID 17443760 DOI: 10.1002/Anie.200700430 |
0.819 |
|
2006 |
Mohr JT, Nishimata T, Behenna DC, Stoltz BM. Catalytic enantioselective decarboxylative protonation. Journal of the American Chemical Society. 128: 11348-9. PMID 16939246 DOI: 10.1021/Ja063335A |
0.817 |
|
2006 |
Stoltz B, Mohr J, Nishimata T, Behenna D. Catalytic Enantioselective Decarboxylation-Protonation Synfacts. 2006: 1239-1239. DOI: 10.1055/S-2006-949497 |
0.797 |
|
2005 |
Mohr JT, Behenna DC, Harned AM, Stoltz BM. Deracemization of quaternary stereocenters by Pd-catalyzed enantioconvergent decarboxylative allylation of racemic beta-ketoesters. Angewandte Chemie (International Ed. in English). 44: 6924-7. PMID 16206310 DOI: 10.1002/Anie.200502018 |
0.802 |
|
2005 |
Stoltz B, Mohr J, Behenna D, Harned A. Quaternary Carbon Center Formation by Decarboxylation of Allyl β-Ketoesters Synfacts. 2006: 0053-0053. DOI: 10.1055/S-2005-921674 |
0.765 |
|
2004 |
Behenna DC, Stoltz BM. The enantioselective Tsuji allylation. Journal of the American Chemical Society. 126: 15044-5. PMID 15547998 DOI: 10.1021/Ja044812X |
0.773 |
|
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