1229358-49-9

Upstream product

• 127793-66-2 (4S)-7-{[(tert-butyl)(dimethyl)silyl]oxy}hept-1-en-4-ol 
• 100-39-0 benzyl bromide 
• 866138-79-6 (2S)-5-{[(tert-butyl)(dimethyl)silyl]oxy}-2-hydroxypentyl 4-methylbenzenesulfonate 
• 821-09-0 n-Pent-4-enyl alcohol 
• 127154-84-1 tert-butylpent-4-enyloxydimethylsilane 
• 197229-91-7 (2S)-5-{[(tert-butyl)(dimethyl)silyl]oxy}pentane-1,2-diol 
• 18162-48-6 tert-butyldimethylsilyl chloride 
• 197229-94-0 (tert-butyl)(dimethyl){3-[(2S)-oxiran-2-yl]propoxy}silane 

Downstream Products

• 1229358-52-4 (4S)-4-(benzyloxy)hept-6-en-1-ol 
• 1229358-29-5 (4S)-4-(benzyloxy)hept-6-enoic acid 
• 1229358-24-0 (2R,3R)-3-(benzyloxy)pent-4-en-2-yl (4S)-4-(benzyloxy)hept-6-enoate 
• 1229358-55-7 (5S,7Z,9R,10R)-5,9-bis(benzyloxy)-10-methyl-3,4,5,6,9,10-hexahydro-2H-oxecin-2-one 

Relevant academic research and scientific papers

Asymmetric total synthesis of stagonolide G

A simple asymmetric total synthesis of stagonolide G (1) is described. Asymmetric dihydroxylation, regioselective epoxide ring opening, and vinyl Grignard reactions are involved in generating the stereogenic centers C(4) and C(8), followed by Grubbs-II-ca

First stereoselective total synthesis of stagonolide G

First stereoselective total synthesis of nonenolide stagonolide G involving a convergent strategy is described. The key reactions include Keck allylation and Grubbs ring closing metathesis reaction.