Add to ORKG1518-1525An intramolecular alkylation based approach has been explored for the enantiospecific construction of AB-ring system of taxanes starting from 3-allyl-4,4-dimethylcarvone, which however led only to bicyclo[2.2.2]octanones
A highly stereo- and enantio-selective methodology for the construction of the chiral functionalised...
This thesis describes synthetic studies aimed towards developing a concise synthesis of taxinine, a ...
A short, regio- and stereoselective approach to functionalized cis-bicyclo[6.4.0]dodecane ring syste...
An intramolecular alkylation based approach has been explored for the enantiospecific construction o...
A simple and convenient tandem methodology for the enantiospecific generation of functionalised bicy...
A simple and convenient tandem methodology for the enantiospecific generation of functionalised bicy...
The microbially derived cis-1,2-dihydrocatechol 2 has been converted, via reaction sequences includi...
A simple route for the synthesis of the bicyclo[5.3.1]undecane ring system present in taxanes has be...
In connection with efforts to develop an efficient total synthesis of the biologically active natura...
A domino enyne cross-metathesis/intramolecular Diels-Alder reaction has been successfully used to sy...
Two alternative approaches to the BC-ring system of taxanes, suitable for generating both enantiomer...
Intramolecular pyrylium ylide-alkene cyclizations provide control of the absolute stereochemistry at...
The synthesis of the taxanes derivatives has been the major focus of this research. The efforts made...
The bicyclo[5.4.0]undecenone 4 was converted through a four step sequence involving activation, gem-...
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...
This thesis describes synthetic studies aimed towards developing a concise synthesis of taxinine, a ...
A short, regio- and stereoselective approach to functionalized cis-bicyclo[6.4.0]dodecane ring syste...
An intramolecular alkylation based approach has been explored for the enantiospecific construction o...
A simple and convenient tandem methodology for the enantiospecific generation of functionalised bicy...
A simple and convenient tandem methodology for the enantiospecific generation of functionalised bicy...
The microbially derived cis-1,2-dihydrocatechol 2 has been converted, via reaction sequences includi...
A simple route for the synthesis of the bicyclo[5.3.1]undecane ring system present in taxanes has be...
In connection with efforts to develop an efficient total synthesis of the biologically active natura...
A domino enyne cross-metathesis/intramolecular Diels-Alder reaction has been successfully used to sy...
Two alternative approaches to the BC-ring system of taxanes, suitable for generating both enantiomer...
Intramolecular pyrylium ylide-alkene cyclizations provide control of the absolute stereochemistry at...
The synthesis of the taxanes derivatives has been the major focus of this research. The efforts made...
The bicyclo[5.4.0]undecenone 4 was converted through a four step sequence involving activation, gem-...
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...
This thesis describes synthetic studies aimed towards developing a concise synthesis of taxinine, a ...
A short, regio- and stereoselective approach to functionalized cis-bicyclo[6.4.0]dodecane ring syste...