812649-72-2

Upstream product

• 812649-71-1 (S)-4-benzyl-3-{(2S,3R,4S)-3-hydroxy-5-[(4-methoxybenzyl)oxy]-2,4-dimethylpentanoyl}oxazolidin-2-one 

Downstream Products

• 812649-82-4 1-[(3S,4R,5S,6S)-4-(tert-Butyl-dimethyl-silanyloxy)-2-hydroxy-6-isopropenyl-3,5-dimethyl-cyclohex-1-enyl]-ethanone 
• 812649-75-5 (3R,4S,5R,6S)-2-Acetyl-5-(tert-butyl-dimethyl-silanyloxy)-3-isopropenyl-4,6-dimethyl-cyclohexanone 
• 845522-60-3 (2S,3R,4S,5R,6RS)-3-(tert-butyldimethylsilyloxy)-6-[3-(4-methoxybenzyloxy)-2-methylpropionyl]-2,4,5-trimethylcyclohexanone 
• 845522-58-9 (2RS)-2-methyl-3-oxo-3-[(1S,5S,6R)-1,3,5,6-tetramethyl-2-oxocyclohex-3-enyl]propionic acid 
• 845522-61-4 (2S,3R,4S,8S)-1-[(S)-4-benzyl-2-oxo-oxazolidin-3-yl]-3-(tert-butyldimethylsilyloxy)-9-(4-methoxybenzyloxy)-2,4,8-trimethylnon-5-ene-1,7-dione 
• 812649-66-4 (E)-(4S,5R,6S)-7-((S)-4-Benzyl-2-oxo-oxazolidin-3-yl)-5-(tert-butyl-dimethyl-silanyloxy)-4,6-dimethyl-7-oxo-hept-2-enoic acid ethyl ester 

Relevant academic research and scientific papers

Formation of highly substituted chiral cyclohexanone derivatives using a tandem conjugate addition/cyclisation

A tandem conjugate addition/cyclisation approach, that allows the synthesis of chiral highly substituted cyclohexanones and cyclohexenones, which is applicable to natural product syntheses has been developed. A tandem conjugate addition/cyclisation approa