Zhanjie Li, Ph.D. - Publications
Affiliations: | 2010 | Chemistry | Emory University, Atlanta, GA |
Area:
synthesis of biologically active natural productsYear | Citation | Score | |||
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2012 | Li Z, Boyarskikh V, Hansen JH, Autschbach J, Musaev DG, Davies HM. Scope and mechanistic analysis of the enantioselective synthesis of allenes by rhodium-catalyzed tandem ylide formation/[2,3]-sigmatropic rearrangement between donor/acceptor carbenoids and propargylic alcohols. Journal of the American Chemical Society. 134: 15497-504. PMID 22924394 DOI: 10.1021/Ja3061529 | 0.687 | |||
2012 | Li Z, Parr BT, Davies HM. Highly stereoselective C-C bond formation by rhodium-catalyzed tandem ylide formation/[2,3]-sigmatropic rearrangement between donor/acceptor carbenoids and chiral allylic alcohols. Journal of the American Chemical Society. 134: 10942-6. PMID 22694052 DOI: 10.1021/Ja303023N | 0.69 | |||
2011 | Parr BT, Li Z, Davies HM. Asymmetric Synthesis of Highly Functionalized Cyclopentanes by a Rhodium- and Scandium-Catalyzed Five-Step Domino Sequence. Chemical Science (Royal Society of Chemistry : 2010). 2: 2378-2382. PMID 22708053 DOI: 10.1039/C1Sc00434D | 0.688 | |||
2011 | Parr BT, Li Z, Davies HML. Asymmetric synthesis of highly functionalized cyclopentanes by a rhodium- and scandium-catalyzed five-step domino sequence Chemical Science. 2: 2378-2382. DOI: 10.1039/c1sc00434d | 0.628 | |||
2010 | Li Z, Davies HM. Enantioselective C-C bond formation by rhodium-catalyzed tandem ylide formation/[2,3]-sigmatropic rearrangement between donor/acceptor carbenoids and allylic alcohols. Journal of the American Chemical Society. 132: 396-401. PMID 19994854 DOI: 10.1021/Ja9075293 | 0.648 | |||
2009 | Nadeau E, Li Z, Morton D, Davies HML. Rhodium carbenoid induced intermolecular C-H functionalization at tertiary C-H bonds Synlett. 151-154. DOI: 10.1055/S-0028-1087388 | 0.612 | |||
2009 | Ventura DL, Li Z, Coleman MG, Davies HML. Intermolecular C-H functionalization versus cyclopropanation of electron rich 1,1-disubstituted and trisubstituted alkenes Tetrahedron. 65: 3052-3061. DOI: 10.1016/J.Tet.2008.11.059 | 0.669 | |||
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