This is an interim version of our Electronic Legal Deposit Catalogue-eJournals and eBooks while we continue to recover from a cyber-attack.
ChemInform Abstract: Regioselective Alkylation Reactions of 2, 4‐Diphenyl‐3H‐1‐benzazepine Give Either 3‐Alkyl‐3H‐1‐benzazepines or 1‐Alkyl‐1H‐1‐benzazepines. Issue 2 (January 2015)
Record Type:
Journal Article
Title:
ChemInform Abstract: Regioselective Alkylation Reactions of 2, 4‐Diphenyl‐3H‐1‐benzazepine Give Either 3‐Alkyl‐3H‐1‐benzazepines or 1‐Alkyl‐1H‐1‐benzazepines. Issue 2 (January 2015)
Main Title:
ChemInform Abstract: Regioselective Alkylation Reactions of 2, 4‐Diphenyl‐3H‐1‐benzazepine Give Either 3‐Alkyl‐3H‐1‐benzazepines or 1‐Alkyl‐1H‐1‐benzazepines.
<abstract abstract-type="main" xml:lang="en"> <title>Abstract</title> <p>Deprotonation of benzazepine (I) followed by reaction with alkyl halides or tosylates give either products of alkylation at C3 or at the nitrogen as well as mixtures of both types of products.</p> </abstract>