Thiyl radical-mediated cyclization of ω-alkynyl O-tert-butyldiphenylsilyloximes-Reference-Cited by-同舟云学术

Thiyl radical-mediated cyclization of ω-alkynyl O-tert-butyldiphenylsilyloximes

Published:2017 Issue:14 Volume:15 Page:3025-3034
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Shibata Nina¹²³,Tsuchiya Takahisa¹²³,Hashimoto Yoshimitsu¹²³^ORCID,Morita Nobuyoshi¹²³,Ban Shintaro¹²³,Tamura Osamu¹²³^ORCID

Affiliation:

1. Showa Pharmaceutical University

2. Machida

3. Japan

Abstract

Treatment of ω-alkynyl O-tert-butyldiphenylsilyloximes with odorless thiol and AIBN gave cyclic O-silylhydroxylamines via a radical process in good yields.

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2017/OB/C7OB00279C

Reference67 articles.

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4. Oxime ethers as versatile precursors in organic synthesis: a review

5. O-Acyl oximes: versatile building blocks for N-heterocycle formation in recent transition metal catalysis

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