1041433-41-3

Upstream product

• 67-56-1 methanol 
• 1041433-40-2 (3aR,5R,6S,6aR)-6-(benzyloxy)-5-((R)-1-(benzyloxy)pent-4-enyl)-2,2-dimethyltetrahydrofuro[2,3-d][1,3]dioxole 

Downstream Products

• 1041433-42-4 (1S,3R,4S,5R)-4-(benzyloxy)-3-((R)-1-(benzyloxy)pent-4-enyl)-2,6-dioxabicyclo[3.1.0]hexane 

Relevant academic research and scientific papers

Mild and efficient chemoselective deprotection of anomeric O-methyl glycosides with trityl tetrafluoroborate

(Chemical Equation Presented) A facile chemoselective deprotection of anomeric O-methyl glycosides has been achieved in good to excellent yields within 10-40 min with use of trityl tetrafluoroborate in dichloromethane at ambient temperatures. The present method is easily implemented and tolerates different functional groups.