A new method is reported for the synthesis of the α,β-unsaturated nitrone moiety characteristic of the stephacidin/avrainvillamide family of bioactive prenylated indole alkaloids. Application to the synthesis of stephacidin analogs and a potential biological probe are showcased.A new method is reported for the synthesis of the α,β-unsaturated nitrone moiety characteristic of the stephacidin/avrainvillamide family of bioactive prenylated indole alkaloids. Application to the synthesis of stephacidin analogs and a potential biological probe are showcased. © 2009 Elsevier Ltd. All rights reserved
The ergot alkaloids are an important subgroup of indole alkaloids as they show a wide range of biolo...
A new indole synthesis is described. The key step involves a novel tin-mediated free radical reactio...
Chapter One of this dissertation focuses on the indole diterpene alkaloid family of natural products...
A new method is reported for the synthesis of the α,β-unsaturated nitrone moiety characteristic of t...
Stephacidin A and its congeners are a collection of secondary metabolites that possess intriguing st...
2006 Fall.Includes bibliographical references.The total synthesis of stephacidin A, avrainvillamide ...
2009 Spring.Includes bibliographical references.Progress towards three potential biosynthetic interm...
AbstractA Unified Approach Toward the Total Syntheses ofPrenylated Indole Alkaloid Natural Productsb...
AbstractA Unified Approach Toward the Total Syntheses ofPrenylated Indole Alkaloid Natural Productsb...
Some novel cyclic ?-aminoacid esters and potential bioactive compounds were prepared via thermal 1,2...
This thesis describes synthetic approaches towards indolizidine and pyrrolidine alkaloids. The total...
This thesis describes synthetic approaches towards indolizidine and pyrrolidine alkaloids. The total...
A unified strategy for the synthesis of congeners of the prenylated indole alkaloids is presented. T...
Chapter one discusses the previous use of synthetic chemistry in biosynthetic studies of natural pro...
A unified strategy for the synthesis of congeners of the prenylated indole alkaloids is presented. T...
The ergot alkaloids are an important subgroup of indole alkaloids as they show a wide range of biolo...
A new indole synthesis is described. The key step involves a novel tin-mediated free radical reactio...
Chapter One of this dissertation focuses on the indole diterpene alkaloid family of natural products...
A new method is reported for the synthesis of the α,β-unsaturated nitrone moiety characteristic of t...
Stephacidin A and its congeners are a collection of secondary metabolites that possess intriguing st...
2006 Fall.Includes bibliographical references.The total synthesis of stephacidin A, avrainvillamide ...
2009 Spring.Includes bibliographical references.Progress towards three potential biosynthetic interm...
AbstractA Unified Approach Toward the Total Syntheses ofPrenylated Indole Alkaloid Natural Productsb...
AbstractA Unified Approach Toward the Total Syntheses ofPrenylated Indole Alkaloid Natural Productsb...
Some novel cyclic ?-aminoacid esters and potential bioactive compounds were prepared via thermal 1,2...
This thesis describes synthetic approaches towards indolizidine and pyrrolidine alkaloids. The total...
This thesis describes synthetic approaches towards indolizidine and pyrrolidine alkaloids. The total...
A unified strategy for the synthesis of congeners of the prenylated indole alkaloids is presented. T...
Chapter one discusses the previous use of synthetic chemistry in biosynthetic studies of natural pro...
A unified strategy for the synthesis of congeners of the prenylated indole alkaloids is presented. T...
The ergot alkaloids are an important subgroup of indole alkaloids as they show a wide range of biolo...
A new indole synthesis is described. The key step involves a novel tin-mediated free radical reactio...
Chapter One of this dissertation focuses on the indole diterpene alkaloid family of natural products...