Practical and Highly Selective Sulfur Ylide Mediated Asymmetric Epoxidations and Aziridinations Using an Inexpensive, Readily Available Chiral Sulfide. Applications to the Synthesis of Quinine and Quinidine-Reference-Cited by-同舟云学术

Practical and Highly Selective Sulfur Ylide Mediated Asymmetric Epoxidations and Aziridinations Using an Inexpensive, Readily Available Chiral Sulfide. Applications to the Synthesis of Quinine and Quinidine

Published:2010-01-26 Issue:6 Volume:132 Page:1828-1830
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Illa Ona¹,Arshad Muhammad¹,Ros Abel¹,McGarrigle Eoghan M.¹,Aggarwal Varinder K.¹

Affiliation:

1. School of Chemistry, University of Bristol, Cantock’s Close, Bristol BS8 1TS, United Kingdom

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja9100276

Reference67 articles.

1. Reviews:

2. Chalcogenides as Organocatalysts

3. Catalytic, Asymmetric Sulfur Ylide-Mediated Epoxidation of Carbonyl Compounds: Scope, Selectivity, and Applications in Synthesis

4. dAggarwal, V. K., Crimmin, M., and Riches, S.Science of Synthesis; George Thieme Verlag: Stuttgart, Germany, 2008; Vol. 37, p321.

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