94390-47-3

Upstream product

• 94390-43-9 Acetic acid (R)-5-methyl-1-oxa-spiro[2.5]oct-5-ylmethyl ester 
• 1193-18-6 3-methylcyclohexen-2-one 
• 94390-40-6 (R)-3-hydroxymethyl-3-methylcyclohexanone 
• 94390-39-3 ((2S,3S,7R)-2,3,7-Trimethyl-1,4-dioxa-spiro[4.5]dec-7-yl)-methanol 
• 94390-38-2 7-Methyl-1,4-dioxa-spiro[4.5]decane-7-carboxylic acid methyl ester 
• 56294-19-0 methyl 1-methyl-3-oxocyclohexane-1-carboxylate 
• 33235-14-2 1-methyl-3-oxocyclohexane-1-carbonitrile 

Downstream Products

• 94390-44-0 Acetic acid (R)-3-hydroxymethyl-1-methyl-cyclohex-2-enylmethyl ester 
• 94390-45-1 Acetic acid (R)-3-hydroxymethyl-1-methyl-cyclohex-3-enylmethyl ester 
• 94390-50-8 Acetic acid (R)-3-(tert-butyl-dimethyl-silanyloxymethyl)-1-methyl-cyclohex-3-enylmethyl ester 
• 94390-48-4 Acetic acid (R)-3-(tert-butyl-dimethyl-silanyloxymethyl)-1-methyl-cyclohex-2-enylmethyl ester 
• 94390-49-5 ((R)-3-Benzenesulfonylmethyl-3-methyl-cyclohex-1-enylmethoxy)-tert-butyl-dimethyl-silane 

Relevant academic research and scientific papers

Chemical Transformation of Terpenoids. VII. Syntheses of Chiral Segments, Key Building-Blocks for the Right Half of Taxane-Type Diterpenoids

Two kinds of chiral segments, i.e. segment B-I (4) and segment B-II (5), which are potentially versatile building-blocks for construction of the right half of taxane-type diterpenoids, were synthesized from 3-methyl-2-cyclohexen-1-one (6) via optical reso