99016-98-5

Upstream product

• 99016-97-4 (Z)-7-(benzyloxy)hept-2-en-1-ol 
• 78999-24-3 5-benzyloxy-1-pentanal 
• 100-39-0 benzyl bromide 
• 786668-19-7 methyl (Z)-7-(benzyloxy)hept-2-enoate 
• 4541-15-5 5-(benzyloxy)-1-pentanol 
• 111-29-5 1 ,5-pentanediol 

Downstream Products

• 786668-23-3 (2S,3S)-(+)-7-benzyloxy-2-methylheptane-1,3-diol 
• 99017-00-2 (S)-4-((S)-5-Benzyloxy-1-hydroxy-pentyl)-[1,3]dioxolan-2-one 
• 786668-31-3 {(S)-2-[(2S,6R)-6-But-3-enyl-6-(4-methoxy-benzyloxy)-tetrahydro-pyran-2-yl]-propoxy}-tert-butyl-diphenyl-silane 
• 786668-40-4 (2S,3S)-(-)-7-benzyloxy-1-tert-butyldiphenylsilyloxy-2-methylheptan-3-ol 
• 786668-29-9 (9S,10S)-11-(tert-Butyl-diphenyl-silanyloxy)-9-hydroxy-10-methyl-undec-1-en-5-one 
• 786668-25-5 6-methyl-7-(tert-butyldiphenylsilyl)heptane-1,5-diol 
• 786668-27-7 (S)-6-[(S)-2-(tert-Butyl-diphenyl-silanyloxy)-1-methyl-ethyl]-tetrahydro-pyran-2-one 
• 99016-99-6 Phenyl-carbamic acid (2R,3S)-3-(4-benzyloxy-butyl)-oxiranylmethyl ester 

Relevant academic research and scientific papers

Access to both anomers of pectenotoxin spiroketals by kinetic spiroketalization

A concise synthesis of both AB ring spiroisomers of the pectenotoxins is described. The nonanomeric AB spiroketal ring system of the pectenotoxins-1, -2, -3, and -6 is formed under very mild, kinetic spiroketalization conditions, along with the anomeric i

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