Catalyst and transition-metal free 1,6-conjugate addition of azobisisobutyronitrile: access to isobutyronitrile containing diarylmethanes
Title | Catalyst and transition-metal free 1,6-conjugate addition of azobisisobutyronitrile: access to isobutyronitrile containing diarylmethanes |
Publication Type | Journal Article |
Year of Publication | 2025 |
Authors | Mamale, AG, Ghodake, BM, Gonnade, RG, Bhattacharya, AK |
Journal | Organic & Biomolecular Chemistry |
Volume | 23 |
Issue | 16 |
Pagination | 3956-3966 |
Date Published | APR |
Type of Article | Article |
ISSN | 1477-0520 |
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. |
DOI | 10.1039/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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