81566-29-2

Upstream product

• 94390-39-3 ((2S,3S,7R)-2,3,7-Trimethyl-1,4-dioxa-spiro[4.5]dec-7-yl)-methanol 
• 94390-42-8 (2S,3S,7R)-2,3,7-Trimethyl-7-phenylsulfanylmethyl-1,4-dioxa-spiro[4.5]decane 
• 94390-38-2 7-Methyl-1,4-dioxa-spiro[4.5]decane-7-carboxylic acid methyl ester 
• 94390-33-7 (R)-3-Bromomethyl-3-methyl-cyclohexanone 
• 94390-34-8 (R)-7-Bromomethyl-7-methyl-1,4-dioxa-spiro[4.5]decane 
• 56294-19-0 methyl 1-methyl-3-oxocyclohexane-1-carboxylate 
• 33235-14-2 1-methyl-3-oxocyclohexane-1-carbonitrile 
• 1193-18-6 3-methylcyclohexen-2-one 
• 94390-35-9 (R)-7-Methyl-7-phenylsulfanylmethyl-1,4-dioxa-spiro[4.5]decane 
• 107-21-1 ethylene glycol 

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