99838-64-9

Upstream product

• 600728-54-9 (3S,4R)-4-(Tetrahydro-pyran-2-yloxy)-hept-6-en-3-ol 
• 99884-73-8 (2R,3S)-3-benzyloxy-1-tosyloxy-2-pentanol 
• 99884-73-8 (2R)-3-benzyloxy-1-tosyloxy-2-pentanol 
• 99838-62-7 (2R,3RS)-3-O-benzylpentane-1,2,3-triol 
• 558459-27-1 (1R)-1-[(1S)-oxiranyl]-but-3-en-1-ol 
• 924-41-4 1,5-hexadiene-3-ol 
• 600728-55-0 2-[(R)-1-((S)-1-Benzyloxy-propyl)-but-3-enyloxy]-tetrahydro-pyran 
• 1826-67-1 vinyl magnesium bromide 
• 99838-63-8 (2R,3S)-3-benzyloxy-1,2-epoxypentane 
• 99838-63-8 (2R)-3-benzyloxy-1,2-epoxypentane 

Downstream Products

• 600728-56-1 [(R)-1-((S)-1-Benzyloxy-propyl)-but-3-enyloxy]-acetic acid 
• 99838-81-0 (4S,5S)-4,5-dibenzyloxy-1-heptene 
• 99838-82-1 (3S,4S)-3,4-dibenzyloxyhexanal 
• 99838-67-2 (3R,4S)-3,4-dibenzyloxyhexanal 
• 99944-99-7 (6S,7S)-6,7-dibenzyloxy-3-nonen-2-one 
• 99944-98-6 (6R,7S)-6,7-dibenzyloxy-3-nonen-2-one 
• 600728-65-2 (2R,7R)-2-((S)-1-Benzyloxy-propyl)-7-[(Z)-(S)-1-(tert-butyl-dimethyl-silanyloxy)-6-trimethylsilanyl-hex-3-en-5-ynyl]-2,3,6,7-tetrahydro-oxepine 
• 600728-64-1 {(Z)-(S)-1-[(2R,7R)-7-((S)-1-Benzyloxy-propyl)-2,3,6,7-tetrahydro-oxepin-2-yl]-4-iodo-but-3-enyloxy}-tert-butyl-dimethyl-silane 
• 600728-57-2 (S)-3-{(R)-2-[(R)-1-((S)-1-Benzyloxy-propyl)-but-3-enyloxy]-pent-4-enoyl}-4-isopropyl-oxazolidin-2-one 
• 600728-63-0 (S)-3-[(2R,7R)-7-((S)-1-Benzyloxy-propyl)-2,3,6,7-tetrahydro-oxepin-2-yl]-3-(tert-butyl-dimethyl-silanyloxy)-propan-1-ol 
• 600728-69-6 (S)-3-[(2R,7R)-7-((S)-1-Benzyloxy-propyl)-2,3,6,7-tetrahydro-oxepin-2-yl]-3-(tert-butyl-dimethyl-silanyloxy)-propionaldehyde 
• 600728-58-3 (S)-3-[(2R,7R)-7-((S)-1-Benzyloxy-propyl)-2,3,6,7-tetrahydro-oxepine-2-carbonyl]-4-isopropyl-oxazolidin-2-one 
• 600728-53-8 (S)-3-{2-[(R)-1-((S)-1-Benzyloxy-propyl)-but-3-enyloxy]-acetyl}-4-isopropyl-oxazolidin-2-one 
• 600728-52-7 (R)-2-[(R)-1-((S)-1-Benzyloxy-propyl)-but-3-enyloxy]-pent-4-en-1-ol 

Relevant academic research and scientific papers

Enantioselective total synthesis of (+)-rogioloxepane A

(Matrix presented) The enantioselective synthesis of (+)-rogioloxepane A has been achieved in 21 steps from 1,5-hexadien-3-ol. The key steps in the synthesis are an asymmetric glycolate alkylation leading to the diene 2 and a subsequent ring-closing metat

Enantio- and Diastereocontrolled Synthesis of Chiral 1,2-Diol Derivatives from (R)-2,3-Di-O-isopropylideneglyceraldehyde: endo- and exo-Brevicomin

All four possible stereoisomers of the insect pheromone brevicomin have been prepared from (R)-2,3-di-O-isopropylideneglyceraldehyde (1) on stereocontrolled routes with ee more than 98-99percent.