103795-13-7Relevant academic research and scientific papers
Iterative, Stereoselective Homologation of Chiral Polyalkoxy Aldehydes Employing 2-(Trimethylsilyl)thiazole as a Formyl Anion Equivalent. The Thiazole Route to Higher Carbohydrates
Dondoni, Alessandro,Fantin, Giancarlo,Fogagnolo, Marco,Medici, Alessandro,Pedrini, Paola
, p. 693 - 702 (2007/10/02)
A new approach to long-chain sugars is demonstrated by the stereoselective conversion of D-glyceraldehyde acetonide (2a), L-threose acetonide (2b), and dialdogalactopyranose diacetonide (2h) into higher homologues up to C9, C7, and C
DIASTEREOSELECTIVITY IN THE 1,2-ADDITION OF SILYLAZOLES TO CHIRAL ALDEHYDES. STEREOCONTROLLED HOMOLOGATION OF α-HYDROXYALDEHYDES.
Dondoni, Alessandro,Fogagnolo, Marco,Medici, Alessandro,Pedrini, Paola
, p. 5477 - 5480 (2007/10/02)
The addition of 2-trimethylsilylazoles (thiazole, benzothiazole, oxazole) to α-asymmetryc aldehydes give the corresponding O-silylcarbinols in good chemical yield and high stereoselectivity; the reaction is employed for the stereoselective homologation of
