Catalytic decarbonylation of epoxyaldehydes: applications to the preparation of terminal epoxides
B Morandi, EM Carreira
Index: Morandi, Bill; Carreira, Erick M. Synlett, 2009 , # 13 p. 2076 - 2078
Full Text: HTML
Citation Number: 3
Abstract
The catalytic decarbonylation of aldehydes has become a well-known reaction since its discovery by Tsuji and Ohno. [¹] We previously used this reaction in a new strategy to access chiral building blocks in high optical purity, using the aldehyde as a removable steering group. [²] More recently, Madsen has used the catalytic decarbonylation of unprotected aldoses to generate polyols. [³] Herein we describe a procedure for the decarbonylation of epoxyaldehydes ...
Related Articles:
Efficient Catalytic Corey–Chaykovsky Reactions Involving Ketone Substrates
[Kavanagh, Sarah A.; Piccinini, Alessandro; Connon, Stephen J. Advanced Synthesis and Catalysis, 2010 , vol. 352, # 11-12 p. 2089 - 2093]
In situ formation and reactions of chloromethyl-lithium under sonochemical conditions
[Einhorn, Cathy; Allavena, Corinne; Luche, Jean-Louis Journal of the Chemical Society, Chemical Communications, 1988 , # 5 p. 333 - 334]