| Literature DB >> 27176454 |
Ya-Nan Wu1, Rong Fu1, Nan-Nan Wang1, Wen-Juan Hao1, Guigen Li2, Shu-Jiang Tu1, Bo Jiang1.
Abstract
A new copper-catalyzed sulfur-enabled dehydrobicyclization of 1,6-enynes using potassium sulfide as a sulfurating reagent has been established, providing a straightforward access toward arylated indeno[1,2-c]thiophenes with moderate to good yields. This sulfur incorporation pathway involves Michael addition, 5-exo-dig/5-endo-trig bicyclization and dehydrogenation sequence, resulting in continuous multiple bond-forming events including C-S and C-C bonds to rapidly construct functional organic molecules.Entities:
Mesh:
Substances:
Year: 2016 PMID: 27176454 DOI: 10.1021/acs.joc.6b00692
Source DB: PubMed Journal: J Org Chem ISSN: 0022-3263 Impact factor: 4.354