182880-82-6

Upstream product

• 182880-73-5 (5R,6R)-2,6-dimethyl-5-(1-methylethenyl)-6-((E)-4-methyl-5-oxo-3-hexenyl)-2-cyclohexen-1-one 
• 182880-75-7 (5R,6R)-6-[(E)-5-(tert-Butyl-dimethyl-silanyloxy)-4-methyl-hexa-3,5-dienyl]-5-isopropenyl-2,6-dimethyl-cyclohex-2-enone 
• 182880-77-9 (4aR,4bS,8aR,10aR)-7-(tert-Butyl-dimethyl-silanyloxy)-2,4b,8,10a-tetramethyl-4a,4b,5,6,8a,9,10,10a-octahydro-4H-phenanthren-1-one 
• 182880-78-0 (1aS,1bR,3aR,7aR,7bS,9aR)-9a-(tert-Butyl-dimethyl-silanyloxy)-1a,3a,5,7b-tetramethyl-1,1a,1b,2,3,3a,7,7a,7b,8,9,9a-dodecahydro-cyclopropa[a]phenanthren-4-one 
• 212185-22-3 (5R,6R)-6-(3,3-diethoxypropyl)-2,6-dimethyl-5-(1-methylethenyl)-2-cyclohexen-1-one 
• 183072-24-4 3-[(1R,6R)-1,3-dimethyl-6-(1-methylethenyl)-2-oxo-3-cyclohexenyl]-1-propanal 
• 158930-44-0 6-methyl-carvone 
• 2244-16-8 (S)-p-mentha-6,8-dien-2-one 
• 182880-79-1 (1aS,1bR,3aR,5S,7aR,7bS,9aR)-9a-(tert-Butyl-dimethyl-silanyloxy)-1a,3a,5,7b-tetramethyl-tetradecahydro-cyclopropa[a]phenanthren-4-one 

Downstream Products

• 75657-53-3 stypodiol 

Relevant academic research and scientific papers

An efficient stereoselective synthesis of stypodiol and epistypodiol

An efficient synthesis of stypodiol (1) and its epimer at C-14, epistypodiol (2), was accomplished starting from (S)-(+)-carvone (7). The synthesis of both epimeric compounds proceeds through common intermediates using an IMDA reaction, a sonochemical Barbier reaction, and an acid- catalyzed quinol-tertiary alcohol cyclization as key synthetic steps.