[引用][C] Highly Active Chiral Ruthenium Catalysts for Asymmetric Cross‐and Ring‐Opening Cross‐Metathesis

JM Berlin, SD Goldberg… - Angewandte Chemie …, 2006 - Wiley Online Library
JM Berlin, SD Goldberg, RH Grubbs
Angewandte Chemie International Edition, 2006Wiley Online Library
Olefin metathesis has found widespread application in smallmolecule synthesis.[1] Its use
can be subclassified into three transformations [1a]—ring-opening metathesis, ring-closing
metathesis, and cross-metathesis—and one can readily envision an asymmetric variant of
each of these reactions (Scheme 1). We report herein the use of highly active chiral
ruthenium catalysts for asymmetric ring-opening cross-metathesis (AROCM) and the first
example of an asymmetric cross-metathesis (ACM) reaction. Chiral molybdenum catalysts …
Olefin metathesis has found widespread application in smallmolecule synthesis.[1] Its use can be subclassified into three transformations [1a]—ring-opening metathesis, ring-closing metathesis, and cross-metathesis—and one can readily envision an asymmetric variant of each of these reactions (Scheme 1). We report herein the use of highly active chiral ruthenium catalysts for asymmetric ring-opening cross-metathesis (AROCM) and the first example of an asymmetric cross-metathesis (ACM) reaction.
Chiral molybdenum catalysts have been developed for asymmetric ring-closing metathesis(ARCM) and AROCM.[2–4] These catalysts lack extensive tolerance of functional groups and require rigorous exclusion of air and moisture. The use of more stable enantioselective ruthenium metathesis catalysts, which have a greater tolerance of
Wiley Online Library
以上显示的是最相近的搜索结果。 查看全部搜索结果