Transition Metal-Mediated Syntheses of Alkaloids - Agarwal, Sameer
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Transition Metal-Mediated Syntheses of Yohimbane and Indolizidine Alkaloids. Iron-Mediated [2+2+1] Cycloaddition for the Syntheses of Indole Alkaloids: Total syntheses of Alloyohimbane and 3-Epialloyohimbane; Formal synthesis of Rauniticine and syntheses of various substituted nor-yohimbane alkaloids; Efficient total synthesis of demethoxycarbonyldihydrogambirtannine. Silver(I)-promoted Syntheses of Pyrroles: A novel silver(I)-promoted oxidative cyclization methodology for the synthesis of substituted pyrroles; Total synthesis of Harmicine, and Crispine A.

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Produktbeschreibung
Transition Metal-Mediated Syntheses of Yohimbane and Indolizidine Alkaloids. Iron-Mediated [2+2+1] Cycloaddition for the Syntheses of Indole Alkaloids: Total syntheses of Alloyohimbane and 3-Epialloyohimbane; Formal synthesis of Rauniticine and syntheses of various substituted nor-yohimbane alkaloids; Efficient total synthesis of demethoxycarbonyldihydrogambirtannine. Silver(I)-promoted Syntheses of Pyrroles: A novel silver(I)-promoted oxidative cyclization methodology for the synthesis of substituted pyrroles; Total synthesis of Harmicine, and Crispine A.
Autorenporträt
Dr. Sameer Agarwal has received Ph.D. degree from Technical University, Dresden, Germany in the field of Organic Chemistry under direction of Prof. Dr. Hans-Joachim Knölker, and Master in Chemistry from Indian Institute of Technology, (IIT), Delhi, India. His multifaceted experience is sought for association with several committees and programs.