66529-33-7

Upstream product

• 75265-49-5 3-deuteriocyclohex-2-en-1-one 
• 5323-87-5 3-Ethoxycyclohex-2-en-1-one 
• 66529-38-2 C₇H₁₁⁽²⁾H 

Relevant academic research and scientific papers

Microbiological Reduction of Cyclohexenones by Growing Clostridium Cells

2-Deuterio-2-cyclohexen-1-one, 3-deuterio-2-cyclohexen-1-one and 2-methyl-2-cyclohexen-1-one were reduced by Clostridium La 1 giving a single bioconversion product resulting from reduction of the carbon-carbon double bond.Stereochemistry of the reaction was studied.

Optical Rotatory Dispersion Studies. 133. Deuterium Octant Contributions in Cyclohexanones

The synthesis of four conformationally rigid monodeuterium-substituted cyclohexanones, (2R,4R)-4-isopropyl(2-2H1)cyclohexanone (1), (2S,4R)-4-isopropyl(2-2H1)cyclohexanone (2), (3R,4R)-4-tert-butyl(3-2H1)-cyclohexanone (3), and (3S,4R)-4-tert-butyl(3-2H1)

Microbiological Synthesis of Optically Active 3-Deuterio-cycloalkanones

Optically active 3-deuterio-cyclopentanone and 3-deuterio-cyclohexanone have been prepared by microbiological reduction of 3-deuterio αβ-unsaturated cyclic ketones by Beauveria sulfurescens.