1403989-92-3

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• 308279-03-0 [(3aR,5R,6S,6aR)-2,2-dimethyl-6-(prop-2-yn-1-yloxy)tetrahydro-2H-furo[2,3-d][1,3]dioxol-5-yl]methanol 
• 3433-80-5 1-Bromo-2-bromomethyl-benzene 
• 582-52-5 1,2:5,6-di-O-isopropylidene-α-D-glucofuranose 
• 67441-18-3 (3aR,4S,5R,6aR)-5-(2,2-dimethyl-[1,3]dioxolan-4R-yl)-2,2-dimethyl-6-prop-2-ynyloxy-tetrahydrofuro[2,3-d][1,3]dioxole 

Relevant academic research and scientific papers

Intramolecular base-free sonogashira reaction for the synthesis of benzannulated chiral macrocycles embedded in carbohydrate templates

A base-free, intramolecular Sonogashira reaction-based general approach has been established for the diversity-oriented synthesis (DOS) of fused bi- and tricyclic systems containing benzannulated, 10- to 13-membered chiral macrocycles embedded in carbohydrate templates. Macrocycles with different ring sizes have been prepared by pre-designing the chiral building blocks. Base-sensitive groups like acetyl and TBDPS survived the reaction conditions. Copyright