Practical Syntheses of Enantiomerically Enriched γ-Lactones and γ-Hydroxy Ketones by the Alkylation of Pseudoephedrine Amides with Epoxides and Their Derivatives-Reference-Cited by-同舟云学术

Practical Syntheses of Enantiomerically Enriched γ-Lactones and γ-Hydroxy Ketones by the Alkylation of Pseudoephedrine Amides with Epoxides and Their Derivatives

Published:1996-01-01 Issue:7 Volume:61 Page:2428-2440
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Myers Andrew G.¹,McKinstry Lydia¹

Affiliation:

1. Arnold and Mabel Beckman Laboratories of Chemical Synthesis, California Institute of Technology, Pasadena, California 91125

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo952032o

Reference39 articles.

1. Use of Pseudoephedrine as a Practical Chiral Auxiliary for Asymmetric Synthesis

2. A one-step synthesis of pseudoephedrine glycinamide, a versatile precursor for the synthesis of α-amino acids

3. Practical method for the synthesis of D- or L-.alpha.-amino acids by the alkylation of (+)- or (-)-pseudoephedrine glycinamide.

4. The first practical method for asymmetric epoxidation

5. Catalytic asymmetric epoxidation and kinetic resolution: modified procedures including in situ derivatization

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