The complete structure of Psymberin was determined with the application of the Universal NMR database approach. A formal synthesis of psymberin was completed with the application of spirodiepoxides. An assembly of a dihydroisocumarin ring was accomplished from a complex aldehyde and an anion derived from a pentasubstituted arene. A new condition to couple an aldehyde and an amide was achieved to reach a carbinolamide moiety. This condition was applied for the synthesis of analogs and hybrid structures. In a separate study, a metal and a ligand were investigated to promote the coupling between thioacids and azides.Ph.D.Includes bibliographical referencesby Sezgin Kire
A novel chlorohydrin-based spirocyclization reaction has been developed that complements contemporar...
Spiro compounds provide attractive targets in drug discovery due to their inherent three-dimensional...
Natural products have until recently provided the only remedy for treatment of diseases. The develop...
Two synthetic approaches to psymberin have been accomplished. A highly convergent first generation s...
A comprehensive treatment of the latest research in, and applications of, spiro compoundsSpiro Compo...
The addition of nucleophiles to SDEs (SDEs), the double oxidation product of allenes, offers a conci...
Disclosed are studies on the mechanism and reactivity of spirodiepoxides (SDE) and their application...
The first chapter describes our preparation of novel analogs of the natural product, palmarumycin CP...
An investigation of the pederin family of natural products has led to the total synthesis of theoped...
Revealed are studies on the reactivity and mechanism of spirodiepoxides and their utilization in the...
933-942Diarylidene ketones 1a-c, prepared by the condensation of acetone with different appropriate...
This study was designed to create a series of spirolactone compounds produced through an oxidative s...
This dissertation describes studies toward the total synthesis of purpuromycin. Consisting of naphth...
Modern synthetic methods aim at high efficiency in terms of atom economy and yield while at the same...
A convergent approach for the stereoselective synthesis of diverse spiroethers is described. The rea...
A novel chlorohydrin-based spirocyclization reaction has been developed that complements contemporar...
Spiro compounds provide attractive targets in drug discovery due to their inherent three-dimensional...
Natural products have until recently provided the only remedy for treatment of diseases. The develop...
Two synthetic approaches to psymberin have been accomplished. A highly convergent first generation s...
A comprehensive treatment of the latest research in, and applications of, spiro compoundsSpiro Compo...
The addition of nucleophiles to SDEs (SDEs), the double oxidation product of allenes, offers a conci...
Disclosed are studies on the mechanism and reactivity of spirodiepoxides (SDE) and their application...
The first chapter describes our preparation of novel analogs of the natural product, palmarumycin CP...
An investigation of the pederin family of natural products has led to the total synthesis of theoped...
Revealed are studies on the reactivity and mechanism of spirodiepoxides and their utilization in the...
933-942Diarylidene ketones 1a-c, prepared by the condensation of acetone with different appropriate...
This study was designed to create a series of spirolactone compounds produced through an oxidative s...
This dissertation describes studies toward the total synthesis of purpuromycin. Consisting of naphth...
Modern synthetic methods aim at high efficiency in terms of atom economy and yield while at the same...
A convergent approach for the stereoselective synthesis of diverse spiroethers is described. The rea...
A novel chlorohydrin-based spirocyclization reaction has been developed that complements contemporar...
Spiro compounds provide attractive targets in drug discovery due to their inherent three-dimensional...
Natural products have until recently provided the only remedy for treatment of diseases. The develop...