Substrate Control in Enantioselective and Diastereoselective Aldol Reaction by Memory of Chirality: A Rapid Access to Enantiopure β-Hydroxy Quaternary α-Amino Acids-Reference-Cited by-同舟云学术

Substrate Control in Enantioselective and Diastereoselective Aldol Reaction by Memory of Chirality: A Rapid Access to Enantiopure β-Hydroxy Quaternary α-Amino Acids

Published:2014-01-16 Issue:3 Volume:16 Page:788-791
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Viswambharan Baby¹,Gori Didier¹,Guillot Régis¹,Kouklovsky Cyrille¹,Alezra Valérie¹

Affiliation:

1. Institut de Chimie Moléculaire et des Matériaux d'Orsay (ICMMO-UMR 8182), Univ. Paris-Sud, CNRS, Bât 410, Orsay F-91405 France

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol403523e

Reference24 articles.

1. Recent progress on the stereoselective synthesis of acyclic quaternary α-amino acids

2. Recent approaches towards the asymmetric synthesis of α,α-disubstituted α-amino acids

3. Enantio‐ and Diastereoselective Construction of α,α‐Disubstituted α‐Amino Acids for the Synthesis of Biologically Active Compounds

4. Total Synthesis of Natural tert-Alkylamino Hydroxy Carboxylic Acids

5. Synthesis of α-Amino Acids Based on Chiral Tricycloiminolactone Derived from Natural (+)-Camphor

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