In a study directed toward the bioactive natural product garsubellin A, an expedient route to the bicyclo 3.3.1]nonan-9-one bearing tricyclic core, with a bridgehead anchored tetrahydrofuran ring, is delineated. The approach emanating from commercially available dimedone involved a DIBAL-H mediated retro aldol/re-aldol cyclization cascade and a PCC mediated oxidative cyclization as the key steps. (C) 2013 Elsevier Ltd. All rights reserved
Garsubelone A (1), the first dimeric polycyclic polyprenylated acylphloroglucinols type metabolite f...
The first chemical synthesis of pentacyclic onocerane triterpenoids has been achieved. A putative bi...
Thesis (Ph.D.)--Boston University PLEASE NOTE: Boston University Libraries did not receive an Autho...
In a study directed toward the bioactive natural product garsubellin A, an expedient route to the bi...
An exceptionally concise and stereoselective route to the prenylated bicyclo[3.3.1]nonan-9-one core ...
Bridgehead lithiations have successfully been carried out on substrates derived from catechinic acid...
The bicyclo[3.3.1]nonane architecture is a privileged structural motif found in over 1000 natural pr...
The first enantiospecific approach to garsubellin A and related phloroglucin natural product nemoros...
The synthesis of polyprenylated phloroglucinol natural products, including clusianone, nemorosone, a...
In this two-part dissertation, several different strategies are developed to attempt concise synthes...
A highly diastereoselective single-step cyclization reaction provides access to the bicyclo[3.3.1]no...
Synthetic efforts towards various meroterpenoid natural products based on biosynthetic speculation w...
This thesis outlines synthetic efforts towards three different natural product families. Norascyrono...
The synthesis and the biological evaluation of a new family diterpenes are presented. The synthetic ...
An organic synthesis ‘round trip’ between natural product total synthesis and the development of new...
Garsubelone A (1), the first dimeric polycyclic polyprenylated acylphloroglucinols type metabolite f...
The first chemical synthesis of pentacyclic onocerane triterpenoids has been achieved. A putative bi...
Thesis (Ph.D.)--Boston University PLEASE NOTE: Boston University Libraries did not receive an Autho...
In a study directed toward the bioactive natural product garsubellin A, an expedient route to the bi...
An exceptionally concise and stereoselective route to the prenylated bicyclo[3.3.1]nonan-9-one core ...
Bridgehead lithiations have successfully been carried out on substrates derived from catechinic acid...
The bicyclo[3.3.1]nonane architecture is a privileged structural motif found in over 1000 natural pr...
The first enantiospecific approach to garsubellin A and related phloroglucin natural product nemoros...
The synthesis of polyprenylated phloroglucinol natural products, including clusianone, nemorosone, a...
In this two-part dissertation, several different strategies are developed to attempt concise synthes...
A highly diastereoselective single-step cyclization reaction provides access to the bicyclo[3.3.1]no...
Synthetic efforts towards various meroterpenoid natural products based on biosynthetic speculation w...
This thesis outlines synthetic efforts towards three different natural product families. Norascyrono...
The synthesis and the biological evaluation of a new family diterpenes are presented. The synthetic ...
An organic synthesis ‘round trip’ between natural product total synthesis and the development of new...
Garsubelone A (1), the first dimeric polycyclic polyprenylated acylphloroglucinols type metabolite f...
The first chemical synthesis of pentacyclic onocerane triterpenoids has been achieved. A putative bi...
Thesis (Ph.D.)--Boston University PLEASE NOTE: Boston University Libraries did not receive an Autho...