A synthesis of the fully functionalized A-ring of taxoids from the commercially available monoterpenic chiron R-carvone is outlined. In this approach, regio- and stereoselective restructuring of alkyl substituents and functionalities is effected on the periphery while retaining the six membered core of carvone
1430-1436Enantiospecific syntheses of B-seco-nortaxanes have been accomplished starting from the r...
A chiral five-membered, silyl enol ether containing, steroid ring D precursor has been synthesized f...
An approach to construct enantiopure complex natural product-like frameworks, including the first re...
A synthesis of the fully functionalized A-ring of taxoids from the commercially available monoterpen...
Enantiospecific synthesis of functionalised chiral C-ring derivatives of taxanes, starting from R-ca...
A highly stereo-and enantio-selective methodology for the construction of the chiral functionalised ...
A highly stereo- and enantio-selective methodology for the construction of the chiral functionalised...
Starting from (R)-carvone, the synthesis of chiral, functionalised C-aromatic-B-seco-taxanes and an ...
Department of Organic Chemistry, Indian Institute of Science, Bangalore-560 012 Manuscript received...
Chemical synthesis of natural products is typically inspired by the structure and function of a targ...
Chemical synthesis of natural products is typically inspired by the structure and function of a targ...
An enantiospecific approach to functionalised C-aromatic-8,9-seco-taxanes starting from the readily ...
Carvone is a sustainable and readily available starting material for organic synthesis. Herein, we p...
A stereoselective conversion of the readily available (+)-car-3-ene into (+)-carvone by two differen...
Two alternative approaches to the BC-ring system of taxanes, suitable for generating both enantiomer...
1430-1436Enantiospecific syntheses of B-seco-nortaxanes have been accomplished starting from the r...
A chiral five-membered, silyl enol ether containing, steroid ring D precursor has been synthesized f...
An approach to construct enantiopure complex natural product-like frameworks, including the first re...
A synthesis of the fully functionalized A-ring of taxoids from the commercially available monoterpen...
Enantiospecific synthesis of functionalised chiral C-ring derivatives of taxanes, starting from R-ca...
A highly stereo-and enantio-selective methodology for the construction of the chiral functionalised ...
A highly stereo- and enantio-selective methodology for the construction of the chiral functionalised...
Starting from (R)-carvone, the synthesis of chiral, functionalised C-aromatic-B-seco-taxanes and an ...
Department of Organic Chemistry, Indian Institute of Science, Bangalore-560 012 Manuscript received...
Chemical synthesis of natural products is typically inspired by the structure and function of a targ...
Chemical synthesis of natural products is typically inspired by the structure and function of a targ...
An enantiospecific approach to functionalised C-aromatic-8,9-seco-taxanes starting from the readily ...
Carvone is a sustainable and readily available starting material for organic synthesis. Herein, we p...
A stereoselective conversion of the readily available (+)-car-3-ene into (+)-carvone by two differen...
Two alternative approaches to the BC-ring system of taxanes, suitable for generating both enantiomer...
1430-1436Enantiospecific syntheses of B-seco-nortaxanes have been accomplished starting from the r...
A chiral five-membered, silyl enol ether containing, steroid ring D precursor has been synthesized f...
An approach to construct enantiopure complex natural product-like frameworks, including the first re...
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