109985-75-3Relevant academic research and scientific papers
Asymmetric Intramolecular Conjugate Addition of Amines to Chiral Vinyl Sulphoxides. Total Synthesis of (R)-(+)-Carnegine
Pyne, Stephen G.,Chapman, Sandra L.
, p. 1688 - 1689 (1986)
The (E)- and (Z)-vinyl sulphoxides (3) and (4) upon treatment with base, undergo cyclization to give chiral isoquinolines one of which was converted into (R)-(+)-carnegine.
Stereochemistry of the Intermolecular and Intramolecular Conjugate Additions of Amines and Anions to Chiral (E)- and (Z)-Vinyl Sulfoxides. Total Syntheses of (R)-(+)-Carnegine and (+)- and (-)-Sedamine
Pyne, Stephen G.,Bloem, Peter,Chapman, Sandra L.,Dixon, Christine E.,Griffith, Renate
, p. 1086 - 1093 (2007/10/02)
The intramolecular addition of incipient amine anions to chiral (E)- and (Z)-vinyl sulfoxides occurs in the same diastereofacial sense, giving chiral isoquinoline and piperidine derivatives that differ in relative stereochemistry at C-2.In contrast, the conjugate addition reactions of (E)- and (Z)-β-styryl p-tolyl sulfoxide wih benzylamine and LiCH(CO2Et)2 are diastereoconvergent processes.The same major diastereomeric product is obtained in each case.We have attempted to rationalize the stereochemical outcome of the addition of nucleophiles to chiral vinyl sulfoxides according to the type of nucleophilic reagent employed (either chelating/hydrogen bonding or nonchelating) and from a consideration of possible transition states.
