Highly enantioselective oxonium ylide formation and Stevens rearrangement catalyzed by chiral dirhodium(II) carboxamidates
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference13 articles.
1. Ylide formation from the reaction of carbenes and carbenoids with heteroatom lone pairs
2. Synthesis of allenes by [2,3]-sigmatropic rearrangement of prop-2-yn-1-yl oxonium ylides formed in rhodium(II) carboxylate catalysed reactions of diazo compounds
3. Profound Catalyst Effects in the Generation and Reactivity of Carbenoid-Derived Cyclic Ylides
4. Stereoselective synthesis of the bicyclic core structure of the highly oxidised sesquiterpene neoliacinic acid
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