Chemoenzymatic Synthesis of α-Hydroxy-β-methyl-γ-hydroxy Esters: Role of the Keto−Enol Equilibrium To Control the Stereoselective Hydrogenation in a Key Step-Reference-Cited by-同舟云学术

Chemoenzymatic Synthesis of α-Hydroxy-β-methyl-γ-hydroxy Esters: Role of the Keto−Enol Equilibrium To Control the Stereoselective Hydrogenation in a Key Step

Published:2010-02-09 Issue:5 Volume:75 Page:1410-1418
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Milagre Cíntia D. F.¹,Milagre Humberto M. S.²,Moran Paulo J. S.¹,Rodrigues J. Augusto R.¹

Affiliation:

1. Institute of Chemistry, University of Campinas−UNICAMP, PO Box 6154, 13084-970 Campinas, SP, Brazil

2. Institute of Biosciences, UNESP−Univ. Estadual Paulista, 13506-900 Rio Claro, SP, Brazil

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo902227f

Reference70 articles.

1. Highly Diastereo- and Enantioselective Reactions of Enecarbamates with Ethyl Glyoxylate To Give Optically Activesyn andantiα-Alkyl-β-Hydroxy Imines and Ketones

2. Total Synthesis and Structural Elucidation of Khafrefungin

3. Advances in the Total Synthesis of Biologically Important Marine Macrolides

4. Modern Aldol Methods for the Total Synthesis of Polyketides

5. New opportunities for biocatalysis: making pharmaceutical processes greener

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