912365-49-2

Upstream product

• 57618-47-0 5-benzyloxy-1-pentyne 
• 106-95-6 allyl bromide 
• 5390-04-5 pent-1-yn-5-ol 
• 100-39-0 benzyl bromide 

Downstream Products

• 912365-56-1 (R)-4-Benzyl-3-[(2R,3S,9S)-9-(tert-butyl-diphenyl-silanyloxy)-3-hydroxy-2-(4-methoxy-benzyloxy)-decanoyl]-oxazolidin-2-one 
• 912365-57-2 (R)-4-Benzyl-3-[(2R,3S,9S)-9-(tert-butyl-diphenyl-silanyloxy)-2,3-dihydroxy-decanoyl]-oxazolidin-2-one 
• 912365-54-9 (7-benzyloxy-1-methyl-hept-3-ynyloxy)-tert-butyl-diphenyl-silane 
• 1027582-83-7 7-(tert-butyl-diphenyl-silanyloxy)-octanal 
• 96443-55-9 (-)-cladospolide C 
• 96443-55-9 cladospolide-B 
• 912365-51-6 (R)-2-(6-Benzyloxy-hex-2-ynyl)-oxirane 
• 912365-53-8 (S)-8-Benzyloxy-oct-4-yn-2-ol 
• 912365-50-5 2-(6-benzyloxy-hex-2-ynyl)-oxirane 

Relevant academic research and scientific papers

First synthesis and determination of the absolute stereochemistry of iso-cladospolide-B and cladospolides-B and C

The syntheses of iso-cladospolide-B, cladospolide-B and cladospolide-C are reported with 4S,5S,11S-configuration. Of the three stereogenic centres, the C-4/C-5 vic-diol was created by Evans aldol condensation, while the C-11 stereocentre was created by Ja