Reaction of trimethylaluminium, dimethyllithium cuprate and lithium tetramethylaluminate with the homochiral epoxide 8 has been studied. Intermolecular epoxide ring-opening was observed with dimethyllithium cuprate and lithium tetramethylaluminate, but acetal ring-opening followed by intramolecular epoxide ring-opening was observed with trimethylaluminium
Stereoselective synthesis of a suitably functionalized C-1 to C-15 segment of rapamycin is described
A stereoselective synthesis of a rapamycin fragment is developed and further utilized toward buildin...
The synthesis of the diastereoisomeric epoxides cis-1b-d and trans-2b-d and the products of their ri...
This dissertation describes synthetic studies culminating in the total synthesis of the macrocyclic ...
Details of the total synthesis of rapamycin (1) are reported. The synthesis required the preparation...
This dissertation describes a stereoselective synthesis of two major fragments of rapamycin. Isolate...
The main contributions of the work described in this thesis are the development of a novel method fo...
The macrolide rapamycin ( 1 ) was first described as an antifungal agent in 1975. Even though its bi...
The regiochem. outcome of the ring-opening of epoxides bearing remote polar functionalities was esta...
Résumé Cette thèse consiste en trois thèmes résumés dans les paragraphes ci-dessous. L’influence de...
The synthesis and enantioselective α-deprotonation - double ring opening of 6,7-epoxy-8-azabicyclo[3...
Researchers have long recognized the important physical relationship between molecular conformation ...
For over 30 years, rapamycin has generated a sustained and intense interest from the scientific comm...
The regiochemical control of the ring opening of epoxides bearing polar remote functionalities, thro...
Research toward the total synthesis of the promising antibiotic lactonamycin is reported. Lactonamyc...
Stereoselective synthesis of a suitably functionalized C-1 to C-15 segment of rapamycin is described
A stereoselective synthesis of a rapamycin fragment is developed and further utilized toward buildin...
The synthesis of the diastereoisomeric epoxides cis-1b-d and trans-2b-d and the products of their ri...
This dissertation describes synthetic studies culminating in the total synthesis of the macrocyclic ...
Details of the total synthesis of rapamycin (1) are reported. The synthesis required the preparation...
This dissertation describes a stereoselective synthesis of two major fragments of rapamycin. Isolate...
The main contributions of the work described in this thesis are the development of a novel method fo...
The macrolide rapamycin ( 1 ) was first described as an antifungal agent in 1975. Even though its bi...
The regiochem. outcome of the ring-opening of epoxides bearing remote polar functionalities was esta...
Résumé Cette thèse consiste en trois thèmes résumés dans les paragraphes ci-dessous. L’influence de...
The synthesis and enantioselective α-deprotonation - double ring opening of 6,7-epoxy-8-azabicyclo[3...
Researchers have long recognized the important physical relationship between molecular conformation ...
For over 30 years, rapamycin has generated a sustained and intense interest from the scientific comm...
The regiochemical control of the ring opening of epoxides bearing polar remote functionalities, thro...
Research toward the total synthesis of the promising antibiotic lactonamycin is reported. Lactonamyc...
Stereoselective synthesis of a suitably functionalized C-1 to C-15 segment of rapamycin is described
A stereoselective synthesis of a rapamycin fragment is developed and further utilized toward buildin...
The synthesis of the diastereoisomeric epoxides cis-1b-d and trans-2b-d and the products of their ri...