Catalyst and transition-metal free 1,6-conjugate addition of azobisisobutyronitrile: access to isobutyronitrile containing diarylmethanes

TitleCatalyst and transition-metal free 1,6-conjugate addition of azobisisobutyronitrile: access to isobutyronitrile containing diarylmethanes
Publication TypeJournal Article
Year of Publication2025
AuthorsMamale, AG, Ghodake, BM, Gonnade, RG, Bhattacharya, AK
JournalOrganic & Biomolecular Chemistry
Volume23
Issue16
Pagination3956-3966
Date PublishedAPR
Type of ArticleArticle
ISSN1477-0520
Abstract

A catalyst and transition-metal free 1,6-conjugate addition of azobisisobutyronitrile to para-quinone methides for the synthesis of isobutyronitrile containing diarylmethanes has been achieved. This protocol enables the synthesis of isobutyronitrile containing diarylmethanes in good yields and with a broad substrate scope. This is the first example wherein azobisisobutyronitrile has been used as a cyanide source for 1,6-conjugate addition under catalyst and metal-free conditions.

DOI10.1039/d5ob00012b
Type of Journal (Indian or Foreign)

Foreign

Impact Factor (IF)

2.9

Divison category: 
Organic Chemistry
Database: 
Web of Science (WoS)

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