Short asymmetric synthesis of (2S,3S)- and (2S,3R)-3-prolinoglutamic acids: 2-carboxy-3-pyrrolidine-acetic acids (CPAA)
摘要:
The asymmetric synthesis of both cis and trans 3-prolinoglutamic acids can be easily achieved in a diastereoselective and enantioselective way via the amino zinc-enolate cyclisation. (C) 2002 Elsevier Science Ltd. All rights reserved.
Short asymmetric synthesis of (2S,3S)- and (2S,3R)-3-prolinoglutamic acids: 2-carboxy-3-pyrrolidine-acetic acids (CPAA)
摘要:
The asymmetric synthesis of both cis and trans 3-prolinoglutamic acids can be easily achieved in a diastereoselective and enantioselective way via the amino zinc-enolate cyclisation. (C) 2002 Elsevier Science Ltd. All rights reserved.
Short asymmetric synthesis of (2S,3S)- and (2S,3R)-3-prolinoglutamic acids: 2-carboxy-3-pyrrolidine-acetic acids (CPAA)
作者:Philippe Karoyan、Gérard Chassaing
DOI:10.1016/s0040-4039(01)02129-3
日期:2002.1
The asymmetric synthesis of both cis and trans 3-prolinoglutamic acids can be easily achieved in a diastereoselective and enantioselective way via the amino zinc-enolate cyclisation. (C) 2002 Elsevier Science Ltd. All rights reserved.