900783-33-7

Upstream product

• 900783-32-6 (2S,3S)-3-(benzyloxy)nonane-1,2-diol 
• 98-59-9 p-toluenesulfonyl chloride 

Downstream Products

• 852509-25-2 (4R,5R)-4,5-dibenzyloxyhept-6-enoic acid (1'S,1''S)-1'-(1''-benzyloxyheptyl)-3'-butenyl ester 
• 675127-26-1 1-[1-benzyloxy-(1S)-heptyl]-(1S)-3-butenyl 3-[2,2-dimethyl-5-vinyl-(4R,5R)-1,3-dioxolan-4-yl]propanoate 
• 675127-27-2 (5R,6R,7E,10S)-10-[(1'S)-1'-benzyloxyheptyl]-5,6-isopropylidenedioxy-3,4,5,6,9,10-hexahydro-2H-oxecin-2-one 
• 675127-22-7 1-[1-benzyloxy-(1S)-heptyl]-(1S)-3-butenyl alcohol 
• 900783-34-8 1-benzyloxy-1-[(2S)-oxiran-2-yl]-(1S)-heptane 

Relevant academic research and scientific papers

Enantiodivergent total synthesis of microcarpalide from l-tartaric acid

Stereoselective approach for the synthesis of both enantiomers of bio-active decanolactone microcarpalide is described from l-tartaric acid. The synthesis of the key intermediates en route to the natural product is achieved from l-tartaric acid involving

Stereoselective total synthesis of microcarpalide

A stereoselective total synthesis of microcarpalide using ring-closing metathesis (RCM) as a key step is reported. l-Ascorbic acid was used as a chiral pool material for the construction of the olefinic alcohol and an asymmetric aldol reaction provided the chiral precursor for the synthesis of olefinic acid.