| Literature DB >> 24083568 |
Masato Murai1, Yumi Sota, Yuki Onohara, Jun'ichi Uenishi, Motokazu Uemura.
Abstract
Gold(I)-catalyzed asymmetric intramolecular cyclization of prochiral 1,3-dihydroxymethyl-2-alkynylbenzene or 1,3-bis(carbamate)-2-alkynylbenzene tricarbonylchromium complexes with axially chiral diphosphine ligand gave planar chiral tricarbonylchromium complexes of 1H-isochromene or 1,2-dihydroisoquinoline with high enantioselectivity. An enantiomeric excess of the planar chiral arene chromium complexes was largely affected by a combination of axially chiral diphosphine(AuCl)2 precatalysts and silver salts. In the case of 1,3-dihydroxymethyl-2-alkynylbenzene chromium complexes, a system of segphos(AuCl)2 with AgBF4 resulted in the formation of the corresponding antipode.Entities:
Mesh:
Substances:
Year: 2013 PMID: 24083568 DOI: 10.1021/jo401893f
Source DB: PubMed Journal: J Org Chem ISSN: 0022-3263 Impact factor: 4.354