94292-82-7

Upstream product

• 506-32-1 all cis 5,8,11,14-eicosatetraenoic acid 
• 94235-42-4 4-[(2S,3S)-3-((1E,3E,5Z,7E)-(R)-9-Hydroxy-tetradeca-1,3,5,7-tetraenyl)-oxiranyl]-butyric acid 
• 94235-41-3 4-[(2R,3R)-3-((1E,3E,5E,7E)-(S)-9-Hydroxy-tetradeca-1,3,5,7-tetraenyl)-oxiranyl]-butyric acid ethyl ester 
• 94235-41-3 4-[(2S,3S)-3-((1E,3E,5Z,7E)-(S)-9-Hydroxy-tetradeca-1,3,5,7-tetraenyl)-oxiranyl]-butyric acid ethyl ester 
• 97643-34-0 (7E,9E,11Z,13E)-(5R,6S,15S)-5,6,15-Trihydroxy-icosa-7,9,11,13-tetraenoic acid methyl ester 
• 99017-19-3 (2S,3R)-7-Benzyloxy-heptane-1,2,3-triol 
• 99017-13-7 (7E,9E,13E)-(5R,6S,15S)-5,6,15-Tris-(tert-butyl-dimethyl-silanyloxy)-icosa-7,9,13-trien-11-ynoic acid methyl ester 
• 99017-21-7 2,2-Dimethyl-propionic acid (2S,3R)-7-benzyloxy-2,3-bis-(tert-butyl-dimethyl-silanyloxy)-heptyl ester 
• 99033-15-5 (7E,9E)-(5R,6S)-5,6-Bis-(tert-butyl-dimethyl-silanyloxy)-12-trimethylsilanyl-dodeca-7,9-dien-11-ynoic acid methyl ester 
• 99017-26-2 (7Z,9E)-(5R,6S)-5,6-Bis-(tert-butyl-dimethyl-silanyloxy)-12-trimethylsilanyl-dodeca-7,9-dien-11-ynoic acid methyl ester 
• 99017-23-9 (5R,6S)-5,6-Bis-(tert-butyl-dimethyl-silanyloxy)-7-(2,2-dimethyl-propionyloxy)-heptanoic acid 
• 99017-27-3 (7E,9E)-(5R,6S)-5,6-Bis-(tert-butyl-dimethyl-silanyloxy)-dodeca-7,9-dien-11-ynoic acid methyl ester 
• 99017-22-8 2,2-Dimethyl-propionic acid (2S,3R)-2,3-bis-(tert-butyl-dimethyl-silanyloxy)-7-hydroxy-heptyl ester 
• 99095-34-8 (7E,9E,13E)-(5R,6S,15S)-5,6,15-Trihydroxy-icosa-7,9,13-trien-11-ynoic acid methyl ester 

Relevant academic research and scientific papers

Stereocontrolled Total Synthesis of Lipoxins A

A stereocontrolled total synthesis of lipoxin A and a number of its isomers is reported.The strategy involves Sharpless asymmetric epoxidation and pinylborane asymmetric reduction to build the hydroxy-bearing stereocenters and a Wittig-type as well as a P

SYNTHESIS OF LIPOXINS: TOTAL SYNTHESIS OF CONJUGATED TRIHYDROXY EICOSATETRAENOIC ACIDS

The first synthesis of a conjugated trihydroxy eicosatetraenoic acid, a possible structure for Lipoxin A is described.A biomimetic approach was utilized.