338799-31-8

Upstream product

• 338799-47-6 (2S,3S,5R)-2-(3-Benzyloxy-2-methyl-propyl)-5-(tert-butyl-diphenyl-silanyloxymethyl)-tetrahydro-furan-3-ol 
• 338799-36-3 (2S,3S,5R)-5-(tert-Butyl-diphenyl-silanyloxymethyl)-2-(3-hydroxy-2-methyl-propyl)-tetrahydro-furan-3-ol 
• 338799-33-0 (2S,4S,5S,7RS)-8-O-benzyl-7-methyl-octan-1,2,4,5,8-pentaol 
• 338799-32-9 (2S,3S,5R)-2-[(RS)-3-(1-benzyloxy-2-methyl)]propyl-3-hydroxy-5-(hydroxy)methyltetrahydrofuran 
• 338799-35-2 (+/-)-(E)-1-benzyloxy-2-methyl-4,7-octadiene 
• 338799-44-3 (+/-)-(E)-2-methyl-4,7-octadienoic acid 
• 338799-45-4 (+/-)-(E)-2-methyl-4,7-octadien-1-ol 
• 58479-61-1 tert-butylchlorodiphenylsilane 
• 338799-37-4 (2R,3aS,6R,7aS)-2-(tert-Butyl-diphenyl-silanyloxymethyl)-6-methyl-hexahydro-furo[3,2-b]pyran-5-one 

Downstream Products

• 338799-41-0 (S)-1-[(2R,3aS,5R,6S,7aS)-2-(tert-Butyl-diphenyl-silanyloxymethyl)-5-methoxy-6-methyl-hexahydro-furo[3,2-b]pyran-5-yl]-8-(4-methoxy-benzyloxy)-7-triethylsilanyloxy-oct-4-yn-3-ol 
• 338799-30-7 (Z)-(S)-1-[(2R,3aS,5R,6S,7aS)-2-(tert-Butyl-diphenyl-silanyloxymethyl)-5-methoxy-6-methyl-hexahydro-furo[3,2-b]pyran-5-yl]-8-(4-methoxy-benzyloxy)-7-triethylsilanyloxy-oct-4-en-3-one 
• 338799-48-7 3-[(2R,3aS,5R,6S,7aS)-2-(tert-Butyl-diphenyl-silanyloxymethyl)-5-methoxy-6-methyl-hexahydro-furo[3,2-b]pyran-5-yl]-propan-1-ol 
• 338799-39-6 3-[(2R,3aS,5R,6S,7aS)-2-(tert-Butyl-diphenyl-silanyloxymethyl)-5-methoxy-6-methyl-hexahydro-furo[3,2-b]pyran-5-yl]-propionaldehyde 
• 338799-38-5 ((2R,3aS,5R,6S,7aS)-5-Allyl-5-methoxy-6-methyl-hexahydro-furo[3,2-b]pyran-2-ylmethoxy)-tert-butyl-diphenyl-silane 

Relevant academic research and scientific papers

Highly chemoselective oxidation of 1,5-diols to δ-lactones with TEMPO/BAIB

The selective oxidative conversion of a variety of highly functionalized 1°,2°-1,5-diols into the corresponding δ-lactones has been effected simply and efficiently using a reagent system comprised of catalytic 2,2,6,6-tetramethylpiperidinooxy (TEMPO) and

Synthetic studies toward the C5-C20 domain of the azaspiracids.

[structure: see text]. An approach toward the C5-C20 THF-fused trioxadispiroketal portion of the azaspiracids is reported. The highly substituted azaspiracid D ring (C16-C19) was prepared by the one-pot conversion of a tetraol into a tetrahydrofuran. Effo