Highly stereoselective reduction of β-oxosulfonium salts ---synthesis of trans epoxides----Reference-Cited by-同舟云学术

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Highly stereoselective reduction of β-oxosulfonium salts ---synthesis of trans epoxides---

Published:1984 Issue:42 Volume:25 Page:4779-4782
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Shimagaki Masayuki,Matsuzaki Yuji,Hori Isaburo,Nakata Tadashi,Oishi Takeshi

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference13 articles.

1. M. Shimagaki, T. Maeda, Y. Matsuzaki, I. Hori, T. Nakata, and T. Oishi, Tetrahedron Lett., Submitted.

2. PREPARATION OF OLEFINS BY REDUCTIVE ELIMINATION OF β-HYDROXYSULFIDES USING 2-FLUOROPYRIDINIUM SALT AND LITHIUM IODIDE

3. The preparation of octahydro leukotrienes C, D, and E via a stereoselective sulfenyllactonization reaction

4. Generation of carbon-carbon double bonds from .beta.-oxygenated phenylseleno, phenylthio, and iodo species. A new use for the chlorotrimethylsilane-sodium iodide reagent

5. Chemistry of sulfoxides and related compounds. XLIII. Conversion of ketones to epoxides via .beta.-hydroxy sulfides

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