Highly diastereoselective formation of 1,2,3-trisubstituted cyclopropane derivatives.
Xie, Xingang; Yue, Guoren; Tang, Shouchu; Huo, Xing; Liang, Qiren; She, Xuegong; Pan, Xinfu.
; 7(18): 4057-9, 2005 Sep 01.
Artigo em Inglês | MEDLINE | ID: mdl-16119966
Efficient approaches to the stereoselective synthesis of cyclopropyl alcohols.
First example of highly stereoselective synthesis of 1,2,3-trisubstituted cyclopropanes via chiral selenonium ylides.
Highly Diastereo- and Enantioselective Synthesis of Trifluoromethyl-Substituted Cyclopropanes via Myoglobin-Catalyzed Transfer of Trifluoromethylcarbene.
Indole alkaloids synthesis via a selective cyclization of aminocyclopropanes.
Enantioselective synthesis of 1,2,3-trisubstituted cyclopropanes using gem-dizinc reagents.
Quantification of metabolites for assessing human exposure to soapberry toxins hypoglycin A and methylenecyclopropylglycine.
Synthesis of enantiopure cyclopropyl esters from (-)-levoglucosenone.
Synthesis of [n,5]-spiroketals by ring enlargement of donor-acceptor-substituted cyclopropane derivatives.
Titanium carbenoid-mediated cyclopropanation of allylic alcohols: selectivity and mechanism.
Asymmetric synthesis of cyclopropylamines starting from N-sulfinyl alpha-chloro ketimines.