A Novel Synthesis of α,β,γ,δ-Unsaturated Selenoamides by Using [3,3] Sigmatropic Rearrangement of Alkynyl Propargyl Selenides in the Presence of Diethylamine-Reference-Cited by-同舟云学术

A Novel Synthesis of α,β,γ,δ-Unsaturated Selenoamides by Using [3,3] Sigmatropic Rearrangement of Alkynyl Propargyl Selenides in the Presence of Diethylamine

Published:1994-09 Issue:9 Volume:23 Page:1743-1746
ISSN:0366-7022
Container-title:Chemistry Letters
language:en
Short-container-title:Chem. Lett.

Author:

Shimada Kazuaki,Akimoto Satoru,Itoh Hideki,Nakamura Hidenori,Takikawa Yuji

Publisher

The Chemical Society of Japan

Subject

General Chemistry

Link

https://www.jstage.jst.go.jp/article/cl/23/9/23_9_1743/_pdf

Reference13 articles.

1. Photolysis of isotopically labeled 1,2,3-selenadiazole and 1,2,3-thiadiazole

2. A methodology for the preparation and characterization of three-membered, potentially antiaromatic molecules. Preparation of matrix-isolated thiirene and selenirene

3. Selenium heterocycles. VI. Mechanism of the stereoselective formation of 1,4-diselenafulvenes from 1,2,3-selenadiazoles and base

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