Herein we report the addition of acidic γ-butenolide and N-Boc-pyrrolidone to 4-nitro-5-styrylisoxazoles, a popular class of cinnamic ester synthetic equivalent. The reactions proceeded under the catalysis of Cinchona-based phase-transfer catalysts. Functionalised γ-butenolides were obtained in good isolated yields and moderate enantioselectivity (up to 74% ee)
Bifunctional asymmetric phase-transfer catalysts bearing multiple hydrogen-bonding donors have rarel...
The effectiveness of a series of chiral phase transfer catalysts in cascade reactions of active meth...
A study into the use of a chiral phase-transfer catalyst in conjunction with acetone cyanohydrin to ...
Heavily substituted cyclopropane esters were prepared in high yields, complete diastereoselection an...
This thesis describes an investigation into organocatalysed asymmetric Michael additions and their a...
In this work, we would like to present the development of a highly optimized method for generating t...
Heavily substituted cyclopropane esters were prepared in high yields, complete diastereoselection an...
An asymmetric, phase-transfer-catalyzed vinylogous conjugate addition–vinylogous cyclization cascade...
International audienceAn efficient enantioselective Michael reaction of readily available α‐substitu...
For full abstract, see thesis. The present work deals primarily with the development of two new reac...
A new family of bifunctional H-bond donor phase-transfer catalysts derived from cinchona alkaloids h...
A new family of bifunctional H-bond donor phase-transfer catalysts derived from cinchona alkaloids h...
A novel high yielding, enantio- and diastereoselective protocol for the synthesis of α-allylated hig...
This work is concerned with the development of the synthesis of a series of N-anthracenyl cinchona s...
Readily available chiral ammonium salts derived from cinchona alkaloids have proven to be effective...
Bifunctional asymmetric phase-transfer catalysts bearing multiple hydrogen-bonding donors have rarel...
The effectiveness of a series of chiral phase transfer catalysts in cascade reactions of active meth...
A study into the use of a chiral phase-transfer catalyst in conjunction with acetone cyanohydrin to ...
Heavily substituted cyclopropane esters were prepared in high yields, complete diastereoselection an...
This thesis describes an investigation into organocatalysed asymmetric Michael additions and their a...
In this work, we would like to present the development of a highly optimized method for generating t...
Heavily substituted cyclopropane esters were prepared in high yields, complete diastereoselection an...
An asymmetric, phase-transfer-catalyzed vinylogous conjugate addition–vinylogous cyclization cascade...
International audienceAn efficient enantioselective Michael reaction of readily available α‐substitu...
For full abstract, see thesis. The present work deals primarily with the development of two new reac...
A new family of bifunctional H-bond donor phase-transfer catalysts derived from cinchona alkaloids h...
A new family of bifunctional H-bond donor phase-transfer catalysts derived from cinchona alkaloids h...
A novel high yielding, enantio- and diastereoselective protocol for the synthesis of α-allylated hig...
This work is concerned with the development of the synthesis of a series of N-anthracenyl cinchona s...
Readily available chiral ammonium salts derived from cinchona alkaloids have proven to be effective...
Bifunctional asymmetric phase-transfer catalysts bearing multiple hydrogen-bonding donors have rarel...
The effectiveness of a series of chiral phase transfer catalysts in cascade reactions of active meth...
A study into the use of a chiral phase-transfer catalyst in conjunction with acetone cyanohydrin to ...