115243-97-5

Upstream product

• 118319-77-0 ((3aR,5S,6R,6aR)-6-Benzyloxy-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-yl)-thiazol-2-yl-methanone 
• 79265-30-8 2-(trimethylsilyl)thiazole 
• 23558-05-6 3-O-benzyl-1,2-O-isopropylidene-1,5-D-xylo-dialdofuranose 

Downstream Products

• 118319-77-0 ((3aR,5S,6R,6aR)-6-Benzyloxy-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-yl)-thiazol-2-yl-methanone 
• 115243-98-6 (1S,2R)-2-Benzyloxy-2-((3aR,5R,6S,6aR)-6-benzyloxy-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-yl)-1-thiazol-2-yl-ethanol 
• 115243-99-7 (1R,2R)-2-Benzyloxy-2-((3aR,5R,6S,6aR)-6-benzyloxy-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-yl)-1-thiazol-2-yl-ethanol 
• 115243-95-3 (S)-Benzyloxy-((3aR,5S,6S,6aR)-6-benzyloxy-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-yl)-acetaldehyde 

Relevant 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

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

STEREOSPECIFIC HOMOLOGATION OF D-XYLO AND D-GALACTO DIALDOSES BY 2-TRIMETHYLSILYLTHIAZOLE

Homologation of the title dialdoses is carried out by diastereogenic addition of 2-trimethylsilylthiazole (1) to the side-chain aldehyde and unmasking the formyl group from thiazole ring; further addition of 1 to the resulting homologated dialdoses exhibi