40571-11-7Relevant academic research and scientific papers
NEW POSSIBILITIES FOR CONTROL OF THE TRANSANNULAR CYCLIZATION OF 1,5-DIENES IN THE RITTER REACTION AS ILLUSTRATED BY METHYL-CIS-BICYCLONONA-3,7-DIENES
Nigmatova, V. B.,Andreev, V. A.,Pekhk, T. I.,Belikova, N. A.,Bobyleva, A. A.,et al.
, p. 2213 - 2223 (2007/10/02)
In the Ritter reaction 3-methyl and 3,4-dimethyl-cis-bicyclonona-3,7-dienes are converted either exclusively into acetylamines having the initial structure or into transannular cyclization products of the tricyclo3,7>nonane (brex
