The bicyclo[4.3.0]nonane ring system of the pinguisane-type sesquiterpenoid natural products, including the vicinal quaternary stereocentres, has been synthesised as a single enantiomer via a novel Brønsted acid promoted transannular alkylation of an enol with an unactivated alkene
Enantiopure carbonyl compounds bearing tetrasubstituted α-stereogenic centers are versatile building...
Asymmetric bromolactonization reactions of δ-unsaturated carboxylic acids have been investigated in ...
An enantioselective synthesis of the AB ring system common to the majority of the <i>Schisandra</i> ...
The bicyclo[4.3.0]nonane ring system of the pinguisane-type sesquiterpenoid natural products, includ...
The bicyclo[4.3.0]nonane substructure is an abundant structure found in several natural compounds. A...
Stereo- and regioselective synthesis of chiral bicyclo-[3.3.1]nonanes employing a tandem intermolecu...
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...
A novel three step asymmetric annulation procedure comprises a tandem catalytic enantioselective 1,4...
A novel three step asymmetric annulation procedure comprises a tandem catalytic enantioselective 1,4...
The thesis entitled “Enantioselective synthesis of bio-active bicyclic acetals, cyclic ethers and la...
An enantioselective synthesis of the AB ring system common to the majority of the Schisandra nortrit...
A novel bifunctional catalyst derived from BINOL has been developed that promotes the highly enantio...
The enantiospecific synthesis of several bicyclic enones starting from enantiomerically pure (+)-(1S...
An improved synthetic procedure of racemic bicyclo[3.3.1]nonane-2,6-dione has been developed. Employ...
Enantiopure carbonyl compounds bearing tetrasubstituted α-stereogenic centers are versatile building...
Asymmetric bromolactonization reactions of δ-unsaturated carboxylic acids have been investigated in ...
An enantioselective synthesis of the AB ring system common to the majority of the <i>Schisandra</i> ...
The bicyclo[4.3.0]nonane ring system of the pinguisane-type sesquiterpenoid natural products, includ...
The bicyclo[4.3.0]nonane substructure is an abundant structure found in several natural compounds. A...
Stereo- and regioselective synthesis of chiral bicyclo-[3.3.1]nonanes employing a tandem intermolecu...
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...
A novel three step asymmetric annulation procedure comprises a tandem catalytic enantioselective 1,4...
A novel three step asymmetric annulation procedure comprises a tandem catalytic enantioselective 1,4...
The thesis entitled “Enantioselective synthesis of bio-active bicyclic acetals, cyclic ethers and la...
An enantioselective synthesis of the AB ring system common to the majority of the Schisandra nortrit...
A novel bifunctional catalyst derived from BINOL has been developed that promotes the highly enantio...
The enantiospecific synthesis of several bicyclic enones starting from enantiomerically pure (+)-(1S...
An improved synthetic procedure of racemic bicyclo[3.3.1]nonane-2,6-dione has been developed. Employ...
Enantiopure carbonyl compounds bearing tetrasubstituted α-stereogenic centers are versatile building...
Asymmetric bromolactonization reactions of δ-unsaturated carboxylic acids have been investigated in ...
An enantioselective synthesis of the AB ring system common to the majority of the <i>Schisandra</i> ...