943763-57-3

Upstream product

• 77-76-9 2,2-dimethoxy-propane 
• 270064-36-3 ethyl (E,4R,6R)-7-(benzyloxy)-4,6-dihydroxyhept-2-enoate 
• 14260-66-3 ((3αR,5S,6αR)-2,2-dimethyl-tetrahydrofuro[2,3-d][1,3]dioxol-5-yl)methanol 
• 116431-47-1 (3aR,5R,6aR)-5-[(benzyloxy)methyl]-2,2-dimethyltetrahydrofuro[2,3-d][1,3]dioxole 
• 14260-67-4 (3aR,5R,6aR)-2,2-dimethyl-3a,5,6,6a-tetrahydrofuro[2,3-d][1,3]dioxole-5-carbaldehyde 

Downstream Products

• 943763-58-4 (E)-3-{(4R,6R)-6-[(benzyloxy)methyl]-2,2-dimethyl-1,3-dioxan-4-yl}prop-2-en-1-ol 
• 943763-54-0 (E)-3-{(4R,6R)-6-[(benzyloxy)methyl]-2,2-dimethyl-1,3-dioxan-4-yl}acrylaldehyde 

Relevant academic research and scientific papers

Facile stereoselective synthesis of the C12-C24 fragment of macrolactin-A

A simple and efficient stereoselective synthesis of the C12-C24 fragment of the natural product macrolactin-A was achieved from D-glucose as the starting material and with use of the Wittig and modified Julia olefination reactions as key steps. Georg Thieme Verlag Stuttgart.