Enantioselective synthesis of cis-(2S,3R)- and trans-(2S,3S)-piperidinedicarboxylic acids using domino: allylic acetate and Ireland-Claisen rearrangements and Michael addition as the key steps-Reference-Cited by-同舟云学术

Enantioselective synthesis of cis-(2S,3R)- and trans-(2S,3S)-piperidinedicarboxylic acids using domino: allylic acetate and Ireland-Claisen rearrangements and Michael addition as the key steps

Published:2011-04 Issue:8 Volume:22 Page:872-880
ISSN:0957-4166
Container-title:Tetrahedron: Asymmetry
language:en
Short-container-title:Tetrahedron: Asymmetry

Author:

Garrido Narciso M.,Rosa Sánchez M.,Díez David,Sanz Francisca,Urones Julio G.

Publisher

Elsevier BV

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Catalysis

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5. A facile synthesis of 3-substituted pipecolic acids, chimeric amino acids

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