Por favor, use este identificador para citar o enlazar este ítem: http://hdl.handle.net/10259/3893
Título
Enantioselective Synthesis of Cyclopentadienes by Gold(I)- Catalyzed Cyclization of 1,3-Dien-5-ynes
Autor
Publicado en
Advanced Synthesis & Catalysis. 2013, V. 355, n. 10, p. 1955–1962
Editorial
Wiley-VCH Verlag
Fecha de publicación
2013-07
ISSN
1615-4150
DOI
10.1002/adsc.201300448
Abstract
An asymmetric synthesis of elusive chiral cyclopentadienes has been developed by gold(I)-catalyzed alkoxycyclization of 1,3-dien-5-ynes. The application of these substrates in completely diastereoselective Diels–Alder cycloaddition reactions, which can be carried out in one pot from achiral 1,3-dien-5-ynes, allows the preparation of highly functionalized products bearing five stereogenic centers with high enantiomeric excesses
Palabras clave
cycloisomerization
cyclopentadienes
Diels–Alder reaction
dienynes
gold
Materia
Química orgánica
Chemistry, Organic
Versión del editor
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