The formal synthesis of (+)-sorangicin A was completed by two independent routes. Both approaches feature a cross metathesis reaction to form the C29-C30 bond to arrive at the bicyclic ether/tetrahydropyran fragment. Formation of the C15-C16 olefin to unite the dihydropyran fragment with the rest of the molecule was achieved by either a cross metathesis reaction or a Julia-Kocienski olefination
The jerangolids are a class of natural products with a skipped diene substructure isolated from Sora...
The asymmetric total synthesis of pyranicin (1) is reported. The butenolide ring was constructed via...
(Chemical Equation Presented) An enantioconvergent total synthesis of sordaricin (3), the diterpene ...
The formal synthesis of (+)-sorangicin A was completed by two independent routes. Both approaches fe...
This dissertation has been divided into five chapters, and describes our synthetic efforts towards (...
Efforts towards (+)-sorangicin A, a previously unprepared antibiotic macrolide, are reported. A modu...
The enantioselective total synthesis of spirofungins A and B is reported in 14 steps over the longes...
University of Minnesota Ph.D dissertation. January 2014. Major: Chemistry. Advisor: Andrew M. Harned...
The C11-C17 segment of soraphen A1 with inverted stereochemistry at C17 as required for ring closur...
A carbohydrate derived synthesis of C16-C29 fragment of sorangicin A is described utilizing regiosel...
A novel iodine-catalyzed highly diastereoselective synthesis of trans-2,6-disubstituted-3,4-dihydrop...
The C11–C17 segment of the antifungal agent soraphen A1α was prepared from glyceraldehyde acetonide ...
Part I: A synthetic platform for the total synthesis of the structurally related tetracyclic meroter...
Part I of this thesis describes the total synthesis of 18-deoxynargenicin A$\sb1$. 18-Deoxynargenici...
Chapter one describes a new approach to the synthesis of the antitumour macrolide (+)-acutiphycin, c...
The jerangolids are a class of natural products with a skipped diene substructure isolated from Sora...
The asymmetric total synthesis of pyranicin (1) is reported. The butenolide ring was constructed via...
(Chemical Equation Presented) An enantioconvergent total synthesis of sordaricin (3), the diterpene ...
The formal synthesis of (+)-sorangicin A was completed by two independent routes. Both approaches fe...
This dissertation has been divided into five chapters, and describes our synthetic efforts towards (...
Efforts towards (+)-sorangicin A, a previously unprepared antibiotic macrolide, are reported. A modu...
The enantioselective total synthesis of spirofungins A and B is reported in 14 steps over the longes...
University of Minnesota Ph.D dissertation. January 2014. Major: Chemistry. Advisor: Andrew M. Harned...
The C11-C17 segment of soraphen A1 with inverted stereochemistry at C17 as required for ring closur...
A carbohydrate derived synthesis of C16-C29 fragment of sorangicin A is described utilizing regiosel...
A novel iodine-catalyzed highly diastereoselective synthesis of trans-2,6-disubstituted-3,4-dihydrop...
The C11–C17 segment of the antifungal agent soraphen A1α was prepared from glyceraldehyde acetonide ...
Part I: A synthetic platform for the total synthesis of the structurally related tetracyclic meroter...
Part I of this thesis describes the total synthesis of 18-deoxynargenicin A$\sb1$. 18-Deoxynargenici...
Chapter one describes a new approach to the synthesis of the antitumour macrolide (+)-acutiphycin, c...
The jerangolids are a class of natural products with a skipped diene substructure isolated from Sora...
The asymmetric total synthesis of pyranicin (1) is reported. The butenolide ring was constructed via...
(Chemical Equation Presented) An enantioconvergent total synthesis of sordaricin (3), the diterpene ...