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A direct synthesis of substituted thiophenes via α-oxoketene dithioacetals. II.

✍ Scribed by J.P. Marino; J.L. Kostusyk


Publisher
Elsevier Science
Year
1979
Tongue
French
Weight
195 KB
Volume
20
Category
Article
ISSN
0040-4039

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✦ Synopsis


The regioselective deprotonation of S,S-dimsthyl-a-oxoketene dithioacetal at the (Z)-S-methyl group leads to a direct synthesis of 2-S-methyl-3,4-disubstituted thiophenes.


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## Abstract magnified image 2‐(1‐Benzyl‐1__H__–1,2,3‐triazole‐4‐yl)‐3‐methylsulfanyl‐5‐oxo‐5‐substituted‐__pent__‐2‐enenitrile **3a**, **3b**, **3c**, **3d**, **3e** were obtained in good yields by condensation of (1‐benzyl‐1__H__‐1,2,3‐triazole‐4‐yl)acetonitrile **1** with various α‐oxoketene dit