1337879-22-7

Upstream product

• 1337879-18-1 (4S,5S)-1-(benzyloxy)pentadecane-4,5-diol 
• 1337879-19-2 (4S,5S)-1-benzyloxy-4,5-bis-(tert-butyldimethylsilanyloxy)pentadecane 
• 1337879-20-5 (4S,5S)-4,5-bis-(tert-butyldimethylsilanyloxy)pentadecan-1-ol 
• 1337879-13-6 (4S,5S)-4,5-bis-(tert-butyldimethylsilanyloxy)pentadecanal 
• 1337879-21-6 (4R,7S,8S)-7,8-bis-(tert-butyldimethylsilanyloxy)octadec-1-en-4-ol 
• 1337879-12-5 (4R,7S,8S)-4,7,8-tris(tert-butyldimethylsilanyloxy)octadec-1-ene 
• 261178-56-7 benzyl 11-dodecenoate 
• 69739-34-0 t-butyldimethylsiyl triflate 

Downstream Products

• 949463-70-1 (14S,17S,18S)-N-((3S,11bS)-9,11-bis(benzyloxy)-4-oxo-2,3,4,6,7,11b-hexahydro-1H-pyrido[2,1-a]isoquinolin-3-yl)-14,17,18-trihydroxyoctacosanamide 
• 949463-72-3 (14S,17S,18S)-N-((3S,11bS)-9,11-bis(benzyloxy)-4-oxo-2,3,4,6,7,11b-hexahydro-1H-pyrido[2,1-a]isoquinolin-3-yl)-14,17,18-trihydroxyoctacosanamide 
• 1337879-23-8 C₇₃H₁₂₄N₂O₇Si₃ 
• 1337879-24-9 C₇₃H₁₂₄N₂O₇Si₃ 

Relevant academic research and scientific papers

Formal synthesis of schulzeines B and C

A formal synthesis of schulzeines B and C, marine natural products with inhibitory effect against α-glucosidase, has been achieved. The key reactions of the synthesis are N-acyliminium ion cyclization, Sharpless asymmetric dihydroxylation, olefin cross me