112163-00-5Relevant articles and documents
An efficient synthesis of endo,exo-furofuranone derivatives.
Swain, Nigel A,Brown, Richard C D,Bruton, Gordon
, p. 2042 - 2043 (2002)
The ring openings of 1-acetyl-4-phenyl-3-oxabicyclo[3.1.0]hexane afforded alpha-acetyl-gamma-butyrolactone that underwent a novel diazo-transfer reaction, followed by C-H insertion, to provide a series of endo,exo-furofuranone analogues.
Intramolecular C-H insertions adjacent to sulfur for the diastereoselective synthesis of thienofuranones
Skerry, Paul S.,Swain, Nigel A.,Harrowven, David C.,Smyth, Donald,Bruton, Gordon,Brown, Richard C. D.
, p. 1772 - 1773 (2007/10/03)
A new approach to the diastereoselective synthesis of thienofuranones is described in which an intramolecular 1,5-carbenoid C-H insertion adjacent to sulfur features as a key step.
