The first enantiospecific total synthesis of (-)-9-pupukeanone, starting from (R)-carvone employing a combination of Michael-Michael reaction and an intramolecular rhodium carbenoid C H insertion reaction as key steps, is described. (C) 2002 Elsevier Science Ltd. All rights reserved
A short approach to (+/-)-2-pupukeanone, starting from 2,6-dimethylcyclohexenone employing a combina...
Intramolecular alkylation reaction of the bromoenone 12, obtained from S-carvone in three steps, fur...
A formal total synthesis of the marine sesquiterpene (±)-9-isocyanoneopupukeanane starting from the ...
The first enantiospecific total synthesis of (-)-9-pupukeanone, starting from (R)-carvone employing ...
The first enantiospecific total synthesis of (−)-9-pupukeanone, starting from (R)-carvone employing ...
The first enantiospecific total synthesis of (+)-2-pupukeanone and 5-epi-2-pupukeanone has been achi...
An enantiospecific synthesis of (−)-2-pupukeanone, starting from (R)-carvone employing a Michael–Mic...
The first total synthesis of chiral 2-pupukeanone (+)-4, starting from R-carvone (−)-7 employing a 5...
The first synthesis of a chiral neopupukeanane starting, from (R)-carvone and employing a double Mic...
Intramolecular alkylation reaction of the bromoenone 12, obtained from S-carvone in three steps furn...
The first synthesis of a chiral neopupukeanane starting, from (R)-carvone and employing a double Mic...
Enantiospecific synthesis of both enantiomers of the marine sesquiterpene 2-thiocyanatoneopupukeanan...
1909-1919A combination of intermolecular Michael addition followed by intramolecular Michael additio...
The first total synthesis of (−)-4-thiocyanatoneopupukeanane starting from (R)-carvone has been achi...
The first total synthesis of (-)-4-thiocyanatoneopupukeanane starting from (R)-carvone has been achi...
A short approach to (+/-)-2-pupukeanone, starting from 2,6-dimethylcyclohexenone employing a combina...
Intramolecular alkylation reaction of the bromoenone 12, obtained from S-carvone in three steps, fur...
A formal total synthesis of the marine sesquiterpene (±)-9-isocyanoneopupukeanane starting from the ...
The first enantiospecific total synthesis of (-)-9-pupukeanone, starting from (R)-carvone employing ...
The first enantiospecific total synthesis of (−)-9-pupukeanone, starting from (R)-carvone employing ...
The first enantiospecific total synthesis of (+)-2-pupukeanone and 5-epi-2-pupukeanone has been achi...
An enantiospecific synthesis of (−)-2-pupukeanone, starting from (R)-carvone employing a Michael–Mic...
The first total synthesis of chiral 2-pupukeanone (+)-4, starting from R-carvone (−)-7 employing a 5...
The first synthesis of a chiral neopupukeanane starting, from (R)-carvone and employing a double Mic...
Intramolecular alkylation reaction of the bromoenone 12, obtained from S-carvone in three steps furn...
The first synthesis of a chiral neopupukeanane starting, from (R)-carvone and employing a double Mic...
Enantiospecific synthesis of both enantiomers of the marine sesquiterpene 2-thiocyanatoneopupukeanan...
1909-1919A combination of intermolecular Michael addition followed by intramolecular Michael additio...
The first total synthesis of (−)-4-thiocyanatoneopupukeanane starting from (R)-carvone has been achi...
The first total synthesis of (-)-4-thiocyanatoneopupukeanane starting from (R)-carvone has been achi...
A short approach to (+/-)-2-pupukeanone, starting from 2,6-dimethylcyclohexenone employing a combina...
Intramolecular alkylation reaction of the bromoenone 12, obtained from S-carvone in three steps, fur...
A formal total synthesis of the marine sesquiterpene (±)-9-isocyanoneopupukeanane starting from the ...
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