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Unexpected transformations of camphor (thio)semicarbazones under acetylating conditions

✍ Scribed by Somogyi, László


Book ID
102902323
Publisher
John Wiley and Sons
Year
1991
Tongue
English
Weight
532 KB
Volume
1991
Category
Article
ISSN
0947-3440

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✦ Synopsis


Abstract

The formation of camphor mono‐ and diacetylhydrazones (1, 4, 6) and a stereoselective synthesis of the spirothiadiazoline (1__R__)‐(+)‐2 is described. The degradation of (thio)semicarbazones 3 (X = O, S) and diacetylhydrazone 4 to the acetylhydrazone 6 has been performed.


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Synthesis and Transformation of 3-Coumar
✍ Somogyi, László 📂 Article 📅 1994 🏛 John Wiley and Sons 🌐 English ⚖ 397 KB

## Abstract The synthesis of 3‐acetylcoumarin (thio)acylhydrazones 1a–e and their transformation to 5‐substituted 3‐acetyl‐2‐(3‐coumarinyl)‐2‐methyl‐1,3,4‐oxa(thia)diazolines 2a–f (cyclic isomers of the alternatively accessible diacylhydrazones, e.g. 1f–h) under acetylating conditions are described