Highly Regioselective Palladium-Catalyzed Direct Arylation of Oxazole at C-2 or C-5 with Aryl Bromides, Chlorides, and Triflates-Reference-Cited by-同舟云学术

Highly Regioselective Palladium-Catalyzed Direct Arylation of Oxazole at C-2 or C-5 with Aryl Bromides, Chlorides, and Triflates

Published:2010-07-19 Issue:16 Volume:12 Page:3578-3581
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Strotman Neil A.¹,Chobanian Harry R.¹,Guo Yan¹,He Jiafang¹,Wilson Jonathan E.¹

Affiliation:

1. Department of Process Chemistry and Department of Medicinal Chemistry, Merck Research Laboratories, Merck & Co., Inc., P.O. Box 2000, Rahway, New Jersey 07065

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol1011778

Reference42 articles.

1. For review articles of oxazole-containing natural products, see:

2. Recent advances in the total syntheses of oxazole-containing natural products

3. Muscarine, imidazole, oxazole, and thiazole alkaloids

4. Also known as virginiamycin M1:

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