Synthesis of 2,6-Dideoxysugars via Ring-Closing Olefinic Metathesis
摘要:
graphicGrubbs' RuCl2(=CHPh)(PCy3)(2) (catalyst 1) and RuCl2(=CHPh)(PCy3)(IMess) (catalyst 2) complexes have been successfully utilized in the construction of beta,gamma-unsaturated delta-lactones containing various substitution patterns of methyl groups. Asymmetric dihydroxylation followed by reduction leads to 3,4-cis-dihydroxy-2,6-dideoxypyranoses, which have proven to play very important biological roles as key components of natural products.
Synthesis of 2,6-Dideoxysugars via Ring-Closing Olefinic Metathesis
摘要:
graphicGrubbs' RuCl2(=CHPh)(PCy3)(2) (catalyst 1) and RuCl2(=CHPh)(PCy3)(IMess) (catalyst 2) complexes have been successfully utilized in the construction of beta,gamma-unsaturated delta-lactones containing various substitution patterns of methyl groups. Asymmetric dihydroxylation followed by reduction leads to 3,4-cis-dihydroxy-2,6-dideoxypyranoses, which have proven to play very important biological roles as key components of natural products.
作者:Garry Procter、Andrew T. Russell、Patrick J. Murphy、T.S. Tan、Andrew N. Mather
DOI:10.1016/s0040-4020(01)86648-5
日期:1988.1
Synthesis of 2,6-Dideoxysugars via Ring-Closing Olefinic Metathesis
作者:Peter R. Andreana、Jason S. McLellan、Yongchen Chen、Peng George Wang
DOI:10.1021/ol026710m
日期:2002.10.1
graphicGrubbs' RuCl2(=CHPh)(PCy3)(2) (catalyst 1) and RuCl2(=CHPh)(PCy3)(IMess) (catalyst 2) complexes have been successfully utilized in the construction of beta,gamma-unsaturated delta-lactones containing various substitution patterns of methyl groups. Asymmetric dihydroxylation followed by reduction leads to 3,4-cis-dihydroxy-2,6-dideoxypyranoses, which have proven to play very important biological roles as key components of natural products.