Chemistry of O-silylated ketene acetals1: An efficient synthesis of α-thio--heterocycles from ω-amidosulfoxides by a novel intramolecular pummerer-type rearrangement-Reference-Cited by-同舟云学术

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Chemistry of O-silylated ketene acetals1: An efficient synthesis of α-thio--heterocycles from ω-amidosulfoxides by a novel intramolecular pummerer-type rearrangement

Published:1987-01 Issue:51 Volume:28 Page:6479-6480
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Kita Yasuyuki,Tamura Osamu,Miki Takashi,Tamura Yasumitsu

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference16 articles.

1. Ketene silyl acetals in organic synthesis.

2. A procedure for “iodolactamization”

3. Intramolecular cyclization of ω-primary amino electrophilic olefins to functionalized pyrrolidines and piperidines.

4. Organoselenium-induced cyclization of olefinic imidates and amides. Selective synthesis of lactams or iminolactones

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