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J Org Chem ; 78(21): 10986-95, 2013 Nov 01.
Artigo em Inglês | MEDLINE | ID: mdl-24083568

RESUMO

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.


Assuntos
Alcinos/química , Benzopiranos/síntese química , Cromo/química , Ouro/química , Compostos Organometálicos/síntese química , Benzopiranos/química , Catálise , Compostos Organometálicos/química , Estereoisomerismo
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