Absolute Configurations of Antipodes of γ-Chloro-β-carboxy-β-hydroxybutyric Acid, Chlorocitramalic Acid-Reference-Cited by-同舟云学术

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Absolute Configurations of Antipodes of γ-Chloro-β-carboxy-β-hydroxybutyric Acid, Chlorocitramalic Acid

Published:1971-06 Issue:6 Volume:60 Page:930-933
ISSN:0022-3549
Container-title:Journal of Pharmaceutical Sciences
language:en
Short-container-title:Journal of Pharmaceutical Sciences

Author:

Suh Soon-hee Kim,Hite G.

Publisher

Elsevier BV

Subject

Pharmaceutical Science

Reference14 articles.

1. Stereochemical Investigations of Local Anesthetic Action

2. The Quasi-Favorskii Rearrangement. II.1 Stereochemistry and Mechanism

3. Mechanism and stereochemistry of epoxy ether formation and cleavage IV

4. The Mechanism and Stereochemistry of Formation of (+)-1-Methyl-3-benzoyl-3-hydroxypiperidine from the (-)-3-Halo Analog under Quasi-Favorskii Conditions1a

5. Chemical Preparation of Asymmetrically Labeled Citric Acid1

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3. Persulfate initiated free-radical polymerization of itaconic acid: Kinetics, end-groups and side products;European Polymer Journal;2018-09

4. Pheromone Synthesis, CXLIV. A Synthesis of (1R,5S)-(+)-Frontalin from (S)-(—)-2-Hydroxyparaconic Acid;Liebigs Annalen der Chemie;1992-11-20

5. An efficient entry to highly functionalised C4chiral synthons via Lewis acid-catalysed ene reaction of (1S)-β-pinene and α-keto esters. Part 4.;J. Chem. Soc., Perkin Trans. 1;1990

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