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Investigation by1H NMR of dienediamines as starting materials for the synthesis of indoles and benzofurans by the nenitzescu reaction

✍ Scribed by L. M. Alekseeva; V. M. Lyubchanskaya; T. I. Mukhanova; E. K. Panisheva; V. G. Granik


Book ID
105514507
Publisher
Springer US
Year
1997
Tongue
English
Weight
347 KB
Volume
33
Category
Article
ISSN
0009-3122

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## Abstract The reaction of himachalol with m‐chloroperoxybenzoic acid afforded a rearrangement product, the structure of which was deduced by 2D NMR analysis to be 3Ξ±,4α‐epoxyhimachalane‐2Ξ±,7α‐diol. The recently proposed ^1^H NMR assignments for himachalol have been revised, based on the analysis