Intramolecular dehydrogenative coupling of 2,3-diaryl acrylic compounds: access to substituted phenanthrenes

TitleIntramolecular dehydrogenative coupling of 2,3-diaryl acrylic compounds: access to substituted phenanthrenes
Publication TypeJournal Article
Year of Publication2016
AuthorsGupta, V, Rao, VUBhaskar, Das, T, Vanka, K, Singh, RP
JournalJournal of Organic Chemistry
Volume81
Issue13
Pagination5663-5669
Date PublishedJUL
ISSN0022-3263
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.

DOI10.1021/acs.joc.6b00507
Type of Journal (Indian or Foreign)

Foreign

Impact Factor (IF)4.785
Divison category: 
Physical and Materials Chemistry