A regioselective palladium-free protocol for accessing unsymmetrical biaryls through ring transformation of 6-aryl-~-pyrones


Autoria(s): Kumar, Amit; Singh, Fateh V; Goel, Atul
Data(s)

15/11/2007

15/11/2007

2007

Resumo

A regioselective synthesis of unsymmetrical biaryls with electron withdrawing or donating substituents is described and illustrated by carbanion-induced ring transfonnation of 6-aryl-a-pyrones with methoxyacetone in excellent yield. Our methodology is an alternative to classical organometal-catalyzed aryl-aryl coupling reactions and can be applied to the synthesis of functionally demanding naphthyl biaryls for the development of new ligands for asymetric synthesis

Formato

92259 bytes

application/pdf

Identificador

Tetrahedron Letters 48 (2007) 7283-7286

http://hdl.handle.net/123456789/21

Idioma(s)

en

Relação

C.D.R.I. Communication No. 7255

Palavras-Chave #asymetric synthesis #regioselective #6-aryl-a-pyrones #carbanion-induced ring
Tipo

Article