A concise enantioselective synthesis of (2S,3S)-3-hydroxypipecolic acid via proline catalyzed α-aminooxylation of aldehydes and Pd-catalyzed ether directed aza-Claisen rearrangements-Reference-Cited by-同舟云学术

A concise enantioselective synthesis of (2S,3S)-3-hydroxypipecolic acid via proline catalyzed α-aminooxylation of aldehydes and Pd-catalyzed ether directed aza-Claisen rearrangements

Published:2015-01 Issue:1 Volume:26 Page:24-28
ISSN:0957-4166
Container-title:Tetrahedron: Asymmetry
language:en
Short-container-title:Tetrahedron: Asymmetry

Author:

Ahuja Brij Bhushan,Sudalai Arumugam

Publisher

Elsevier BV

Subject

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

Reference54 articles.

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2. Survival, fecundity and fertility of Bactrocera oleae, as affected by amino acid analogues

3. Inhibition of Glycosphingolipid Biosynthesis: Application to Lysosomal Storage Disorders

4. Sugar-mimic glycosidase inhibitors: natural occurrence, biological activity and prospects for therapeutic application

5. An efficient stereoselective and stereodivergent synthesis of (2R,3R)- and (2R,3S)-3-hydroxypipecolic acids

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