209479-88-9

Upstream product

• 209479-87-8 tert-Butyl-((S)-3,3-dibromo-1-vinyl-allyloxy)-diphenyl-silane 
• 209479-86-7 (2R,3R)-3-O-tert-butyldiphenylsilyl-1,2-O-isopropylidene-4-pentene-1,2,3-triol 
• 223558-55-2 (2R,3S)-3-O-tert-butyldiphenylsilyl-1,2-O-isopropylidene-4-pentene-1,2,3-triol 
• 71769-39-6 (2S,3S,4R)-1,2;3,4-di-O-isopropylidene-5-iodo-1,2,3,4-pentanetetrol 
• 71769-38-5 1-deoxy-2,3-o-isopropylidene-1-tosyl-D-arabinitol 

Downstream Products

• 223558-75-6 tert-Butyl-diphenyl-((Z)-(S)-1-vinyl-pentadec-7-ene-2,4-diynyloxy)-silane 
• 81203-57-8 (3S,9Z)-1,9-heptadecadiene-4,6-diyn-3-ol 
• 87005-03-6 (3R,9R,10R)-panaxytriol 
• 1220632-58-5 C₃₃H₄₂O₂Si 
• 1584730-42-6 C₃₆H₄₆O₃Si 
• 1584730-61-9 C₃₄H₄₂O₄Si 
• 1584730-59-5 C₃₄H₄₂O₄Si 
• 1584730-49-3 C₃₄H₄₂O₃Si 
• 1584730-47-1 (12S,17S,Z)-12-((tert-butyldiphenylsilyl)oxy)-17-ethyloxacycloheptadeca-10-en-13,15-diyn-2-one 
• 1584730-54-0 C₃₄H₄₂O₃Si 
• 1584730-53-9 C₃₄H₄₂O₃Si 
• 1584730-43-7 C₃₆H₄₆O₃Si 
• 1337538-40-5 C₃₃H₄₂O₂Si 
• 209479-94-7 (3R,9R,10R)-10-tert-butyldimethylsilyloxy-3-tert-butyldiphenylsilyloxy-heptadec-1-ene-4,6-diyne-9-ol 

Relevant academic research and scientific papers

Establishment of absolute stereostructure of falcarindiol, algicidal principle against Heterocapsa circularisquama from Notopterygii Rhizoma

Falcarindiol (1) was isolated as an algicidal principle against the harmful red tide dinoflagellate, Heterocapsa circularisquama, from Notopterygii Rhizoma through bioassay-guided separation. In order to determine the ambiguous absolute structure of this

Stereoselective synthesis of (3S,8R,9R,10R)-heptadeca-1-ene-4,6-diyne tetrol and its 3-epimer from D-mannitol

(3S,8R,9R,10R)-Heptadeca-1-ene-4,6-diyne tetrol and its 3-epimer were synthesized, and it was found that the relative configuration which was proposed for 1 was incorrect. Georg Thieme Verlag Stuttgart.

Absolute configuration of falcarinol, a potent antitumor agent commonly occurring in plants

The absolute configuration of falcarinol (1) was established by stereoselective total synthesis of the two enantiomers.

First total synthesis of panaxytriol, a potent antitumor agent isolated from Panax ginseng

Panaxytriol 1, a potent antitumor agent isolated from Panax ginseng, was first synthesized, and its stereostructure was confirmed to be (3R, 9R, 10R)-heptadec-1-ene-4,6-diyne-3,9,10-triol.