1029-1039Enantiospecific synthesis of 3-thapsenol, comprising the carbon framework of a small group of sesquiterpenes containing three contiguous quaternary carbon atoms has been described. (R)-Carvone has been employed as the chiral starting material utilizing the isopropenyl group as a masked hydroxy group. A combination of alkylation, orthoester Claisen rearrangement and intramolecular diazo ketone cyclopropanation reactions has been employed for the creation of the three requisite contiguous quaternary carbon atoms
Enantiospecific total synthesis of optical antipode of the sesquiterpene 5-senecioyloxy-10,11-epoxyt...
An enantiospecific approach to mayurone and thujopsenes, sesquiterpenes containing three contiguous ...
776-788Enantiospecific total synthesis of optical antipode of the sesquiterpene 5-senecioyloxy-10,1...
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...
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...
751-761Synthetic approach to 3-alkoxythapsane, comprising of the carbon framework of a small group...
First enantiospecific total synthesis of optical antipode of the sesquiterpene 10,11-epoxythapsan-...
Synthetic approach to 3-alkoxythapsane, comprising of the carbon framework of a small group of sesqu...
413-422First enantiospecific total synthesis of optical antipode of the sesquiterpene 10,11-epoxytha...
An enantiospecific approach to a functionalised carbon framework of the sesquiterpenes, cyperanes, s...
An enantiospecific synthesis of a thapsane containing an oxygen substituent at the C-3 position is a...
An enantiospecific approach to mayurone and thujopsenes, sesquiterpenes containing three contiguous ...
Enantiospecific total synthesis of optical antipode of the sesquiterpene 5-senecioyloxy-10,11-epoxyt...
An enantiospecific approach to mayurone and thujopsenes, sesquiterpenes containing three contiguous ...
776-788Enantiospecific total synthesis of optical antipode of the sesquiterpene 5-senecioyloxy-10,1...
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...
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...
751-761Synthetic approach to 3-alkoxythapsane, comprising of the carbon framework of a small group...
First enantiospecific total synthesis of optical antipode of the sesquiterpene 10,11-epoxythapsan-...
Synthetic approach to 3-alkoxythapsane, comprising of the carbon framework of a small group of sesqu...
413-422First enantiospecific total synthesis of optical antipode of the sesquiterpene 10,11-epoxytha...
An enantiospecific approach to a functionalised carbon framework of the sesquiterpenes, cyperanes, s...
An enantiospecific synthesis of a thapsane containing an oxygen substituent at the C-3 position is a...
An enantiospecific approach to mayurone and thujopsenes, sesquiterpenes containing three contiguous ...
Enantiospecific total synthesis of optical antipode of the sesquiterpene 5-senecioyloxy-10,11-epoxyt...
An enantiospecific approach to mayurone and thujopsenes, sesquiterpenes containing three contiguous ...
776-788Enantiospecific total synthesis of optical antipode of the sesquiterpene 5-senecioyloxy-10,1...
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