1371603-72-3

Upstream product

• 313963-29-0 (S)-1-((tert-butyldiphenylsilyl)oxy)hex-5-en-2-ol 
• 214914-86-0 1-(4-Methoxybenzyloxy)pent-4-yn-2-ol 
• 165876-55-1 (2S,5S)-5-<(tert-butyldiphenylsiloxy)methyl>tetrahydrofuran-2-methanol 
• 58479-61-1 tert-butylchlorodiphenylsilane 
• 149099-14-9 (2S,5S)-5-<(tert-Butyldiphenylsiloxy)methyl>tetrahydrofuran-2-carboxaldehyde 
• 824-94-2 p-methoxybenzyl chloride 
• 80910-01-6 (R)-2-(((4-methoxybenzyl)oxy)methyl)oxirane 
• 106731-74-2 tert-butyl[(2S)-oxiran-2-ylmethoxy]diphenylsilane 
• 1371603-69-8 (R)-tert-butyl((1-((4-methoxybenzyl)oxy)pent-4-yn-2-yl)-oxy)diphenylsilane 

Downstream Products

• 1384974-76-8 C₃₃H₄₄O₅Si 
• 1371603-73-4 (R)-2-((tert-butyldiphenylsilyl)oxy)-7-((2R,5S)-5-(((tert-butyldiphenylsilyl)oxy)methyl)tetrahydrofuran-2-yl)heptan-1-ol 
• 1371603-74-5 tert-butyl(((2S,5R)-5-((R)-6-((tert-butyldiphenylsilyl)oxy)-7-iodoheptyl) tetrahydrofuran-2-yl)methoxy)diphenylsilane 
• 1371603-82-5 (S)-3-((R)-2-((tert-butyldiphenylsilyl)oxy)-7-((2R,5S)-5-(((tert-butyldiphenylsilyl)oxy)methyl)tetrahydrofuran-2-yl)heptyl)-5-methylfuran-2(5H)-one 
• 1371603-83-6 (S)-3-((R)-2-((tert-butyldiphenylsilyl)oxy)-7-((2R,5S)-5-(hydroxymethyl)tetrahydrofuran-2-yl)heptyl)-5-methylfuran-2(5H)-one 

Relevant academic research and scientific papers

Total synthesis of (-)-goniotrionin

A stereoselective total synthesis of the reported structure of goniotrionin (4) has been accomplished. The key steps involved the opening of a chiral epoxide, a highly diastereoselective Mukaiyama aerobic oxidative cyclization, a selective 1,2-syn Mukaiyama aldol reaction, and a Noyori reduction.