124177-03-3

Upstream product

• 106540-31-2 (+)-(S)-3-(tert-butyldimethylsiloxy)-2,2-dimethylcyclohexanone 
• 109-94-4 formic acid ethyl ester 

Downstream Products

• 124177-04-4 (S)-3-(tert-butyldimethylsilyloxy)-6-(butylthiomethylene)-2,2-dimethylcyclohexanone 
• 124177-06-6 (S)-4-(tert-butyldimethylsilyloxy)-3,3-dimethyl-1-cyclohexenecarbaldehyde 
• 124177-07-7 (S)-4-(tert-butyldimethylsilyloxy)-3,3-dimethyl-1-cyclohexenemethanol 
• 124177-05-5 (S)-3-(tert-Butyl-dimethyl-silanyloxy)-6-[1-butylsulfanyl-meth-(Z)-ylidene]-2,2-dimethyl-cyclohexanol 
• 124177-12-4 (1S,3S,6R)-3-(tert-butyldimethylsilyloxy)-6-hydroxy-2,2,6-trimethylcyclohexaneethanol 
• 124177-11-3 (1S,3S,6S)-3-(tert-butyldimethylsilyloxy)-6-hydroxy-2,2,6-trimethylcyclohexaneethanol 
• 124177-13-5 (1R,3S,6R)-3-(tert-butyldimethylsilyloxy)-6-hydroxy-2,2,6-trimethylcyclohexaneethanol 
• 124177-14-6 (1R,3S,6S)-3-(tert-butyldimethylsilyloxy)-6-hydroxy-2,2,6-trimethylcyclohexaneethanol 
• 124177-09-9 ethyl (1R,3S)-3-hydroxy-2,2-dimethyl-6-methylenecyclohexaneacetate 
• 124263-02-1 ethyl (1S,3S)-3-hydroxy-2,2-dimethyl-6-methylenecyclohexaneacetate 
• 124263-09-8 (1'R,2'R)-1-(3-furyl)-2-(2'-hydroxy-2',6',6'-trimethylcyclohexyl)-1-ethanone 
• 124263-08-7 (1'S,2'S)-1-(3-furyl)-2-(2'-hydroxy-2',6',6'-trimethylcyclohexyl)-1-ethanone 
• 69924-97-6 (1S,1'S,2'S)-1-(3-furyl)-2-(2-'hydroxy-2',6',6'-trimethylcyclohexyl)ethanol 
• 124263-12-3 (1R,1'R,2'R)-1-(3-furyl)-2-(2-'hydroxy-2',6',6'-trimethylcyclohexyl)ethanol 

Relevant academic research and scientific papers

A Synthesis of the carbon skeleton of maoecrystal v □

An enantioselective synthesis of the maoecrystal V (1) carbon skeleton Is described. The key transformations Include arylatlon of a 1,3dicarbonyl compound with a triarylbismuth(V) dichloride species, oxidative dearomatlzatlon of a phenol, and a subsequent

Synthesis of Mono- and Sesquiterpenoids, XIX Synthesis of the Enantiomers of Ancistrofuran, a Defensive Compound from Ancistrotermes cavithorax

The synthesis of the enantiomers (1 and 1') of ancistrofuran was achieved starting from (S)-3-hydroxy-2,2-dimethylcyclohexanone.