Chemospecific Preparation of Both Enantiomers of α‐Terpinyl Trifluoroacetate-Reference-Cited by-同舟云学术

Chemospecific Preparation of Both Enantiomers of α‐Terpinyl Trifluoroacetate

Published:2004-12-31 Issue:3 Volume:34 Page:541-545
ISSN:0039-7911
Container-title:Synthetic Communications
language:en
Short-container-title:Synthetic Communications

Author:

de Mattos Marcio C. S.¹,Coelho Ricardo B.¹,Sanseverino Antonio M.¹

Affiliation:

1. a Instituto de Química, Departamento de Química Orgânica , Universidade Federal do Rio de Janeiro , Caixa Postal 68545, 21945‐970, Rio de Janeiro, Brazil

Publisher

Informa UK Limited

Subject

Organic Chemistry

Link

https://www.tandfonline.com/doi/pdf/10.1081/SCC-120027295

Reference7 articles.

1. A Convenient and Simplified Preparation of Both Enantiomers of α-Terpinyl Chloride

2. Surface-Mediated Chemospecific Hydrobromination of Limonene: Stereoselective transformation of the enantiomers of Limonene into α-Terpinyl Bromide

3. Kinetics and mechanism of addition of acids to olefins. Part 2. Addition of trifluoroacetic acid to (+)-(R)-limonene in weakly polar media

4. TRANSITION METAL SALTS MEDIATED OXIDATIVE RADICAL ADDITION OF ETHYL ACETOACETATE TO LIMONENE

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