56685-62-2Relevant articles and documents
An in-depth study on ring-closing metathesis of carbohydrate-derived α-alkoxyacrylates: Efficient syntheses of DAH, KDO, and 2-deoxy-β-KDO
Hekking, Koen F. W.,Moelands, Marcel A. H.,Van Delft, Floris L.,Rutjes, Floris P. J. T.
, p. 6444 - 6450 (2007/10/03)
Novel, efficient synthetic pathways to DAH, KDO, and 2-deoxy-β-KDO are described. Ring-closing metathesis (RCM) of highly functionalized α-alkoxyacrylate fragments resulted in a series of synthetically versatile oxygen heterocyclic intermediates. Further
ELIMINATIVE DEOXYGENATION: A FACILE SYNTHESIS OF α-CYANO AND α-CARBOALKOXY SUBSTITUTED VINYL SULFIDES
Miller, R. D.,Haessig, R.
, p. 2395 - 2398 (2007/10/02)
The facile eliminative deoxygenation of α-cyano and carboalkoxy sulfoxides by trimethylsilyl triflate under mildly basic conditions results in the formation of α-thiophenyl substituted α,β-unsaturated nitriles and esters in high yields.
NEW ACETYLENIC MICHAEL RECEPTOR EQUIVALENTS. PART I : SYNTHESIS OF α-SULFENYL - AND α-SULFINYL ACRYLIC DERIVATIVES.
Leyendecker, Francois,Comte, Marie-Therese
, p. 5031 - 5034 (2007/10/02)
The synthesis of α-thioarylated β-unsubstituted acrilic derivatives is reported.
