104331-52-4

Upstream product

• 106445-04-9 1-(6-benzyloxy-2,2-dimethyltetrahydrofuro[2,3-d][1,3]dioxol-5-yl)-2-(tert-butyldimethylsiloxy)ethanol 
• 106445-05-0 3-O-benzyl-6-O-tert-butyldimethylsilyl-1,2-O-isopropylidene-α-D-xylo-hexofuran-5-ulose 
• 148236-82-2 (3aR,5S,6S,6aR)-6-Benzyloxy-5-((S)-1-methoxy-1-methyl-allyl)-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxole 
• 148236-81-1 (3aR,5S,6S,6aR)-6-Benzyloxy-2,2-dimethyl-5-((R)-2-vinyl-oxiranyl)-tetrahydro-furo[2,3-d][1,3]dioxole 
• 148236-80-0 (R)-2-((3aR,5S,6S,6aR)-6-Benzyloxy-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-yl)-1-(tert-butyl-dimethyl-silanyloxy)-but-3-en-2-ol 
• 22529-61-9 (1R)-1-((3aR,6S,6aR)-6-(benzyloxy)-2,2-dimethyltetrahydrofuro(2,3-d)(1,3)dioxol-5-yl)ethane-1,2-diol 
• 74-88-4 methyl iodide 
• 100-39-0 benzyl bromide 

Relevant academic research and scientific papers

A formal synthesis of a novel immunosuppressant ISP-1 : Stereocontrolled Pd(O) catalysedcis-hydroxyamination of carbohydrate derived vinyl epoxide

Described herein are the results leading to the synthesis of ISP-1 containing an unusal α, α-disubstituted amino acid and whose immunosuppressive activity only has recently been discovered.

Synthetic Studies of Pyridomycin. IV. Syntheses of Some Twelvemembered Ring Compounds Designed for Construction of Intact Ring System with Exocyclic (Z)-s-Butylidene Side Chain in Pyridomycin

(2R,5R,6S,9S,10S,11R)-10-Hydroxy-2--5,11-dimethyl-9-(3-pyridylmethyl)-6-(benzyloxycarbonylamino)-8-aza-1,4-dioxacyclododecane-3,7-12-trione and its 1'-O-methyl derivative, and (2S,1'R)-diastereomer of the latter have been