68690-80-2

Upstream product

• 55776-46-0 (3'E)-3-(5'-benzyloxy-3'-methylpent-3'-enyl)-2,2-dimethyloxirane 
• 106-24-1 Geraniol 
• 100-39-0 benzyl bromide 
• 52188-73-5 geranyl benzyl ether 

Downstream Products

• 32989-52-9 (E)-4-methyl-6-(phenylmethoxy)-4-hexenal 
• 130648-04-3 (E)-8-Benzyloxy-2-hydroxy-2,6-dimethyl-oct-6-en-3-one 
• 52220-07-2 trans,trans-1-benzyloxy-8-chloro-3,7-dimethyl-2,6-octadiene 
• 68690-51-7 all-trans-1-benzyloxy-3,7,11,15-tetramethyl-9-p-tolylsulfonyl-2,6,10,14-hexadecatetraene 
• 68690-72-2 1-((6Z,10E,14E)-16-Benzyloxy-2,6,10,14-tetramethyl-hexadeca-2,6,10,14-tetraene-8-sulfonyl)-4-methyl-benzene 
• 68690-82-4 Acetic acid (E)-6-benzyloxy-1-isopropenyl-4-methyl-hex-4-enyl ester 
• 68690-78-8 (2E)-1-benzyloxy-6-hydroxy-3,7-dimethyl-2,7-octadiene 
• 130790-60-2 (2E,6R)-1-benzyloxy-3,7-dimethyl-2-octene-6,7-diol 
• 130790-61-3 (S)-3-((E)-5-Benzyloxy-3-methyl-pent-3-enyl)-2,2-dimethyl-oxirane 
• 98066-00-3 (E)-4-methyl-6-(phenylmethoxy)-4-hexen-1-ol 
• 68690-81-3 Acetic acid (E)-6-benzyloxy-1-(1-hydroxy-1-methyl-ethyl)-4-methyl-hex-4-enyl ester 

Relevant academic research and scientific papers

CONVENIENT SYNTHESIS OF CHIRAL EPOXYISOPRENOIDS BY YEAST REDUCTION

The terminal double bond of acyclic isoprenoids was converted into chiral epoxide in high optical yield by using asymmetric reduction of α-ketol with baker's yeast.

Total Syntheses of Fungal Metabolites and Functionalized Furanones

Simple, efficient syntheses of the fungal metabolites colletochlorin D and (+/-)-ascofuranone and one of its stereoisomers are described.Our investigations of functionalized furanones also enabled us to develop a nine-step (22percent overall yield) synthe