162601-68-5

Upstream product

• 86833-19-4 benzyl 3-O-benzyl-4,6-O-benzylidene-α-D-glucopiranoside 

Downstream Products

• 162518-31-2 (S)-5-((2R,4aR,6S,7S,8S,8aR)-6,8-Bis-benzyloxy-7-hydroxy-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-7-yl)-2,2-diethyl-[1,3]dioxolan-4-one 
• 162518-32-3 (2R,4aR,6S,7S,8S,8aR)-6,8-Bis-benzyloxy-7-((4R,5R)-2,2-diethyl-5-hydroxymethyl-[1,3]dioxolan-4-yl)-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-7-ol 

Relevant academic research and scientific papers

Highly functionalized, enantiomerically pure furo[x,y-c]pyrans via alkylidenecarbenes derived from sugar templates: synthesis and mechanism study via computational chemistry

The new method for the generation of alkylidenecarbenes based on the reaction of trimethylsilylazide/Bu2SnO with α-cyanomesylates has been applied to readily available sugar derivatives for the synthesis of highly functionalized, enantiomerical

Synthesis of a peracetylated stereoisomer of De Rosa's calditol: Some questions about the correctness of the original structure assigned to this natural product

Comparison of the 13C nmr spectrum of the nonacetate of a synthetic stereoisomer of calditol with that of the nonacetate of the natural product, combined with a comparison of the 13C nmr spectrum of the peracetate of a hexitol derive