155488-92-9

Upstream product

• 74243-89-3 *R^*)>-α,2,2-trimethyl-1,3-dioxolane-4-ethanol 
• 100-44-7 benzyl chloride 
• 75-24-1 trimethylaluminum 
• 78469-85-9 (2S,3S)-4-benzyloxy-2,3-epoxy-1-butanol 
• 77-76-9 2,2-dimethoxy-propane 

Downstream Products

• 197517-51-4 (4S,5R)-6-Benzyloxy-4-tert-butoxy-5-methyl-hexanal 
• 197517-56-9 (R)-1-[(2R,5S)-5-((R)-2-Benzyloxy-1-methyl-ethyl)-tetrahydro-furan-2-yl]-1-iodo-butan-2-one 
• 197517-85-4 ((R)-1-{(R)-[(2R,5S)-5-((R)-2-Benzyloxy-1-methyl-ethyl)-tetrahydro-furan-2-yl]-iodo-methyl}-propoxy)-tert-butyl-dimethyl-silane 
• 197517-83-2 ((E)-(1R,6S,7R)-8-Benzyloxy-6-tert-butoxy-1-ethyl-7-methyl-oct-2-enyloxy)-tert-butyl-dimethyl-silane 
• 197517-81-0 1-((4S,5R)-6-Benzyloxy-4-tert-butoxy-5-methyl-hexane-1-sulfonyl)-4-methyl-benzene 
• 197517-75-2 Toluene-4-sulfonic acid (4S,5R)-6-benzyloxy-4-tert-butoxy-5-methyl-hexyl ester 
• 197517-58-1 (R)-1-[(2R,5S)-5-((R)-2-Benzyloxy-1-methyl-ethyl)-tetrahydro-furan-2-yl]-butan-2-ol 
• 197517-62-7 (S)-1-[(2R,5S)-5-((R)-2-Benzyloxy-1-methyl-ethyl)-tetrahydro-furan-2-yl]-butan-2-ol 
• 197517-54-7 (E)-(8S,9R)-10-Benzyloxy-8-tert-butoxy-9-methyl-dec-4-en-3-one 
• 197517-60-5 {(R)-1-[(2R,5S)-5-((R)-2-Benzyloxy-1-methyl-ethyl)-tetrahydro-furan-2-ylmethyl]-propoxy}-tert-butyl-dimethyl-silane 
• 197517-73-0 (4S,5R)-6-Benzyloxy-4-tert-butoxy-5-methyl-hexan-1-ol 
• 197517-49-0 ((2R,3S)-3-tert-Butoxy-2-methyl-hept-6-enyloxymethyl)-benzene 
• 197517-77-4 ((2R,3S)-3-tert-Butoxy-6-iodo-2-methyl-hexyloxymethyl)-benzene 
• 197517-47-8 (2R,3S)-1-Benzyloxy-2-methyl-hept-6-en-3-ol 

Relevant academic research and scientific papers

A Formal Synthesis of Aplysiatoxin: Enantioselective Synthesis of Kishi's Aldehyde

This paper describes the enantioselective synthesis of key fragments (12,18,24, and 35) for the synthesis of aplysiatoxin (1a), a potent cancer promoter, and their convergent assembly to Kishi's aldehyde (2).Since 2 has already been transformed into 1a in

Stereoselective Synthesis of erythro-Serricornin, (4R,6R,7S)-, and (4S,6R,7S)-4,6-Dimethyl-7-hydroxynonan-3-one, Stereoisomers of the Sex Pheromone of Cigarette Beetle

A stereoselective synthesis of erythro-serricornin was completed starting from L-(+)-tartaric acid.The relative configuration of C(6)-methyl and C(7)-hydroxyl groups in naturally occurring serricornin was threo.