Add to ORKGThe first enantiospecific synthesis of a thapsane, containing three contiguous quaternary carbon atoms, is accomplished starting from R-carvone. An intramolecular alkylation and an intramolecular diazoketone cyclopropanation reaction were employed for the stereo- and regiospeci®c generation of three contiguous quaternary carbon atoms present in the thapsane framework
The details of the first total synthesis of a natural thapsane lg containing three contiguous quater...
The details of the first total synthesis of a natural thapsane lg containing three contiguous quater...
Stereo- and enantiospecific synthesis of (+)-valerane starting from R-carvone utilising orthoester C...
The first enantiospecific synthesis of a thapsane, containing three contiguous quaternary carbon ato...
The first enantiospecific synthesis of a thapsane, containing three contiguous quaternary carbon ato...
The first enantiospecific synthesis of a thapsane, containing three contiguous quaternary carbon ato...
An enantiospecific synthesis of a thapsane containing an oxygen substituent at the C-3 position is a...
449-459Enantiospecific synthesis of thaps-8-en-5-ol, comprising of the carbon framework of a small g...
Enantiospecific synthesis of thaps-8-en-5-ol, comprising of the carbon framework of a small group of...
First enantiospecific total synthesis of optical antipode of the sesquiterpene 10,11-epoxythapsan-...
1029-1039Enantiospecific synthesis of 3-thapsenol, comprising the carbon framework of a small group...
413-422First enantiospecific total synthesis of optical antipode of the sesquiterpene 10,11-epoxytha...
The first enantiospecific synthesis of (+)-cis,anti,cis-1,8,12,12-tetramethyl-4-oxatricyclo[6.4.0.02...
The enantiospecific first total synthesis of 10-hydroxy-10,11-epoxythapsan-5-yl senecioate (+)-1f, t...
An enantiospecific approach to a functionalised carbon framework of the sesquiterpenes, cyperanes, s...
The details of the first total synthesis of a natural thapsane lg containing three contiguous quater...
The details of the first total synthesis of a natural thapsane lg containing three contiguous quater...
Stereo- and enantiospecific synthesis of (+)-valerane starting from R-carvone utilising orthoester C...
The first enantiospecific synthesis of a thapsane, containing three contiguous quaternary carbon ato...
The first enantiospecific synthesis of a thapsane, containing three contiguous quaternary carbon ato...
The first enantiospecific synthesis of a thapsane, containing three contiguous quaternary carbon ato...
An enantiospecific synthesis of a thapsane containing an oxygen substituent at the C-3 position is a...
449-459Enantiospecific synthesis of thaps-8-en-5-ol, comprising of the carbon framework of a small g...
Enantiospecific synthesis of thaps-8-en-5-ol, comprising of the carbon framework of a small group of...
First enantiospecific total synthesis of optical antipode of the sesquiterpene 10,11-epoxythapsan-...
1029-1039Enantiospecific synthesis of 3-thapsenol, comprising the carbon framework of a small group...
413-422First enantiospecific total synthesis of optical antipode of the sesquiterpene 10,11-epoxytha...
The first enantiospecific synthesis of (+)-cis,anti,cis-1,8,12,12-tetramethyl-4-oxatricyclo[6.4.0.02...
The enantiospecific first total synthesis of 10-hydroxy-10,11-epoxythapsan-5-yl senecioate (+)-1f, t...
An enantiospecific approach to a functionalised carbon framework of the sesquiterpenes, cyperanes, s...
The details of the first total synthesis of a natural thapsane lg containing three contiguous quater...
The details of the first total synthesis of a natural thapsane lg containing three contiguous quater...
Stereo- and enantiospecific synthesis of (+)-valerane starting from R-carvone utilising orthoester C...