High Chelation Control of Three Contiguous Stereogenic Centers in the Reformatsky Reactions of Indium Enolates with α-Hydroxy Ketones: Unexpected Stereochemistry of Lactone Formation-Reference-Cited by-同舟云学术

High Chelation Control of Three Contiguous Stereogenic Centers in the Reformatsky Reactions of Indium Enolates with α-Hydroxy Ketones: Unexpected Stereochemistry of Lactone Formation

Published:2006-06-16 Issue:14 Volume:8 Page:3029-3032
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Babu Srinivasarao Arulananda¹,Yasuda Makoto¹,Okabe Yuji¹,Shibata Ikuya¹,Baba Akio¹

Affiliation:

1. Department of Applied Chemistry, Graduate School of Engineering, Osaka University, 2-1 Yamada-oka, Suita, Osaka 565-0871, Japan

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol060943m

Reference23 articles.

1. Neue Synthese zweiatomiger einbasischer Säuren aus den Ketonen

2. Rhodium-Catalyzed Reformatsky-Type Reaction

3. Low-valent tantalum-mediated reaction

4. Anodic synthesis of butenolides from β-ethylenic esters double cyclization in the presence of olefins

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