600728-55-0

Upstream product

• 558459-27-1 (1R)-1-[(1S)-oxiranyl]-but-3-en-1-ol 
• 924-41-4 1,5-hexadiene-3-ol 
• 100-39-0 benzyl bromide 
• 600728-54-9 (3S,4R)-4-(Tetrahydro-pyran-2-yloxy)-hept-6-en-3-ol 

Downstream Products

• 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 
• 600728-56-1 [(R)-1-((S)-1-Benzyloxy-propyl)-but-3-enyloxy]-acetic acid 
• 600728-59-4 [(2R,7R)-7-((S)-1-Benzyloxy-propyl)-2,3,6,7-tetrahydro-oxepin-2-yl]-methanol 
• 600728-61-8 (2R,7R)-7-((S)-1-Benzyloxy-propyl)-2,3,6,7-tetrahydro-oxepine-2-carbaldehyde 
• 333788-75-3 (Z)-(S)-1-[(2R,7R)-7-((S)-1-Benzyloxy-propyl)-2,3,6,7-tetrahydro-oxepin-2-yl]-hex-3-en-5-yn-1-ol 
• 333788-76-4 (2R,7R)-2-((S)-1-Benzyloxy-propyl)-7-((Z)-(R)-1-chloro-hex-3-en-5-ynyl)-2,3,6,7-tetrahydro-oxepine 
• 99838-64-9 (4R,5S)-5-benzyloxy-1-hepten-4-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