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Journal ArticleDOI

New synthetic route to mono- and di-γδ-unsaturated n,n-dialkylthioamides by the thio-claisen rearrangement based on acyclic n,n-dialkylthioamides

Seiichi Takano, +3 more
- 01 Feb 1977 - 
- Vol. 8, Iss: 5
TLDR
In this article, aus den Thiocarbonsaureamiden (I) mit (II) erhaltenen Sulfoniumbromide (III) ergeben bei der Behandlung mit 1,0-1,2 Molaquival.
Abstract
Die aus den Thiocarbonsaureamiden (I) mit (II) erhaltenen Sulfoniumbromide (III) ergeben bei der Behandlung mit 1,0-1,2 Molaquival.

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References
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Journal ArticleDOI

New synthetic route to mono- and di-γδ-unsaturated NN-dialkylthionamides by the thio-Claisen rearrangement based on acyclic NN-dalkylthioamides

TL;DR: In this paper, a thio-Claisen rearrangement of α-amino-αβ-unsaturated sulphides derived from acyclic NN-dialkylthioamides was proposed.
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