Intramolecular dehydrogenative coupling of 2,3-diaryl acrylic compounds: access to substituted phenanthrenes
Title | Intramolecular dehydrogenative coupling of 2,3-diaryl acrylic compounds: access to substituted phenanthrenes |
Publication Type | Journal Article |
Year of Publication | 2016 |
Authors | Gupta, V, Rao, VUBhaskar, Das, T, Vanka, K, Singh, RP |
Journal | Journal of Organic Chemistry |
Volume | 81 |
Issue | 13 |
Pagination | 5663-5669 |
Date Published | JUL |
ISSN | 0022-3263 |
Abstract | A simple, facile, and environmentally benign intramolecular dehydrogenative coupling of various 1,2-diarylethylenes for the synthesis of phenanthrenes in excellent yield has been described. This new methodology uses ceric ammonium nitrate (CAN) as a promoter at room temperature and has been extended to intermolecular synthesis of biaryl compounds. The electron transfer from methoxyarene to cerium leads to cationic radical formation, which further proceeds to intramolecular coupling. Preliminary mechanistic investigation by EPR spectroscopy and density functional theory calculation suggested a similar view. |
DOI | 10.1021/acs.joc.6b00507 |
Type of Journal (Indian or Foreign) | Foreign |
Impact Factor (IF) | 4.785 |
Divison category:
Physical and Materials Chemistry