| Literature DB >> 26068123 |
Meng-Yang Chang1, Yu-Chieh Cheng1, Yi-Ju Lu1.
Abstract
Intramolecular carbonyl allylation of α-prenyl or α-geranyl β-arylketosulfones 5 in the presence of molecule sieves (MS) affords substituted benzenes 6-7 in moderate to good yields. The facile transformation proceeds by a synthetic sequence starting with the α-prenylation or α-geranylation of 1 and the Bi(OTf)3-mediated annulation of 5 followed by a sequential desulfonative aromatization or then an intramolecular Friedel-Crafts alkylation. A plausible mechanism has been studied and proposed.Entities:
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Year: 2015 PMID: 26068123 DOI: 10.1021/acs.orglett.5b01461
Source DB: PubMed Journal: Org Lett ISSN: 1523-7052 Impact factor: 6.005