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1,5-Asymmetric induction of chirality using π-allyltricarbonyliron lactone complexes: highly diastereoselective synthesis of α-functionalised carbonyl compounds
Christopher J. Hollowood,Steven V. Ley,Edward A. Wright
Organic & Biomolecular Chemistry Pub Date : 08/13/2003 00:00:00 , DOI:10.1039/B306862E
Abstract

Silyl enol ethers derived from ketone functionalised π-allyltricarbonyliron lactone complexes undergo highly diastereoselective carbon–fluorine and carbon–oxygen bond formation reactions with excellent control at the α-stereogenic centre.

Graphical abstract: 1,5-Asymmetric induction of chirality using π-allyltricarbonyliron lactone complexes: highly diastereoselective synthesis of α-functionalised carbonyl compounds
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