Silyl-cupration of an acetylene followed by ring-formation
I Fleming, EM de Marigorta
Index: Fleming, Ian; De Marigorta, Eduardo Martinez Journal of the Chemical Society - Perkin Transactions 1, 1999 , # 8 p. 889 - 900
Full Text: HTML
Citation Number: 27
Abstract
The acetylenes 1a–e undergo silyl-cupration followed by cyclisation, the acetylenes 1f–1h react with the silyl-cuprate reagent more rapidly at the alternative electrophilic site, and the acetylenes 1i, 1j and 17 give relatively low yields of cyclic products amongst others. Ring- formation is, unusually, a not particularly favourable pathway.
Related Articles:
[Oppolzer, Wolfgang; Xu, Jin-Zhu; Stone, Charles Helvetica Chimica Acta, 1991 , vol. 74, # 3 p. 465 - 468]
Study of a Radical Cyclizations Cascade Leading to Bicyclo [3.1. 1] heptanes
[Bogen, Stephane; Fensterbank, Louis; Malacria, Max Journal of Organic Chemistry, 1999 , vol. 64, # 3 p. 819 - 825]
Study of a Radical Cyclizations Cascade Leading to Bicyclo [3.1. 1] heptanes
[Bogen, Stephane; Fensterbank, Louis; Malacria, Max Journal of Organic Chemistry, 1999 , vol. 64, # 3 p. 819 - 825]
Study of a Radical Cyclizations Cascade Leading to Bicyclo [3.1. 1] heptanes
[Bogen, Stephane; Fensterbank, Louis; Malacria, Max Journal of Organic Chemistry, 1999 , vol. 64, # 3 p. 819 - 825]
Study of a Radical Cyclizations Cascade Leading to Bicyclo [3.1. 1] heptanes
[Bogen, Stephane; Fensterbank, Louis; Malacria, Max Journal of Organic Chemistry, 1999 , vol. 64, # 3 p. 819 - 825]