Reaction of Lithiotrimethylsilyldiazomethane with α-Oxoketene Dithioacetals.
✍ Scribed by Rina Miyabe; Takayuki Shioiri; Toyohiko Aoyama
- Publisher
- John Wiley and Sons
- Year
- 2010
- Weight
- 31 KB
- Volume
- 33
- Category
- Article
- ISSN
- 0931-7597
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📜 SIMILAR VOLUMES
The chemoselective and stereoselective addition of organocuprates to cyclic a-oxoketene dithioacetals affords predominately the E vinylogous thioesters. An acyclic a-oxoketene dithioacetal affords the 2 vinylogous thioester stereoselectively. The observed selectivities are dependent upon substrate
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.
## 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