148903-07-5

Upstream product

• 148903-06-4 (1S,4R,4aS,5R,6R,8S,8aR)-6-Vinyl-1,4,4a,5,6,7,8,8a-octahydro-1,4-methano-naphthalene-5,8-diol 
• 148903-03-1 (-)-(1S,4R,4aS,5S,8aS)-5-acetoxy-1,4,4a,8a-tetrahydro-endo-1,4-methanonaphthalen-8(5H)-one 
• 148903-04-2 Acetic acid (1S,4R,4aS,5R,6R,8aR)-8-oxo-6-vinyl-1,4,4a,5,6,7,8,8a-octahydro-1,4-methano-naphthalen-5-yl ester 
• 146830-36-6 (+)-(1S,4R,4aS,5R,8S,8aR)-5-Acetoxy-1,4,4a,5,8,8a-hexahydro-8-hydroxy-endo-1,4-methanonaphthalene 

Downstream Products

• 148903-08-6 (3S,4R,6S)-3,6-Bis-(tert-butyl-dimethyl-silanyloxy)-4-vinyl-cyclohexene 

Relevant academic research and scientific papers

Concise Enantiodivergent Synthesis of Eutypoxide B

The first enantiodivergent synthesis of eutypoxide B 1, a metabolite of the fungus Eutypa lata, has been accomplished in a stereo- and regio-controlled manner by using the single chiral building block 3 as a chiral equivalent of (Z)-cyclohex-2,5-dien-1,4-diol 2.