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General Synthesis of Tetrasubstituted Alkenyl-1,3,4-oxadiazoles.

✍ Scribed by Clint A. James; Brigitte Poirier; Christiane Grise; Alain Martel; Edward H. Ruediger


Book ID
101982457
Publisher
John Wiley and Sons
Year
2006
Weight
23 KB
Volume
37
Category
Article
ISSN
0931-7597

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✦ Synopsis


Abstract

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πŸ“œ SIMILAR VOLUMES


5-(1-Alkenyl)-1, 3, 4-oxadiazol-2(3H)-on
✍ Kurt RΓΌfenacht πŸ“‚ Article πŸ“… 1974 πŸ› John Wiley and Sons 🌐 German βš– 126 KB

## Abstract 3‐(2‐alkenoyl)‐thiocarbazic acid O‐methyl esters **1** are desulfurated by bromine and the unknown intermediates are transformed by alkali to 5‐(1‐alkenyl)‐1, 3, 4‐oxadiazol‐2(3__H__)‐ones (**2**). This type of oxadiazolone substitution is not realizable by the common ring closure of hy