Asymmetric synthesis of 1-alkynylcyclopropane-1-carboxylates
摘要:
Dirhodium tetrakis(S-(N-dodecylbenzenesulfonyl)prolinate)(Rh2S-DOSP4) catalyzed decomposition of methyl alkynyldiazoacetates in the presence of alkenes results in highly diastereoselective and enantioselective cyclopropanations. (C) 2000 Published by Elsevier Science Ltd.
Asymmetric synthesis of 1-alkynylcyclopropane-1-carboxylates
摘要:
Dirhodium tetrakis(S-(N-dodecylbenzenesulfonyl)prolinate)(Rh2S-DOSP4) catalyzed decomposition of methyl alkynyldiazoacetates in the presence of alkenes results in highly diastereoselective and enantioselective cyclopropanations. (C) 2000 Published by Elsevier Science Ltd.
Asymmetric synthesis of 1-alkynylcyclopropane-1-carboxylates
作者:Huw M.L. Davies、Timothy A. Boebel
DOI:10.1016/s0040-4039(00)01453-2
日期:2000.10
Dirhodium tetrakis(S-(N-dodecylbenzenesulfonyl)prolinate)(Rh2S-DOSP4) catalyzed decomposition of methyl alkynyldiazoacetates in the presence of alkenes results in highly diastereoselective and enantioselective cyclopropanations. (C) 2000 Published by Elsevier Science Ltd.