94390-41-7

Upstream product

• 94390-39-3 ((2S,3S,7S)-2,3,7-Trimethyl-1,4-dioxa-spiro[4.5]dec-7-yl)-methanol 
• 192433-20-8 (R)-1-methyl-3-oxocyclohexane-1-carboxylic acid 
• 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 
• 1193-18-6 3-methylcyclohexen-2-one 

Relevant academic research and scientific papers

All-carbon quaternary stereogenic centers by enantioselective Cu-catalyzed conjugate additions promoted by a chiral N-heterocyclic carbene

(Chemical Equation Presented) Necessity is the mother of invention: When the available catalysts do not cut it, a new one has to be developed. A chiral N-heterocyclic carbene (NHC) is used in the first catalytic asymmetric conjugate addition of alkyl- and

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