Date of Award

1-1-2014

Thesis Type

masters

Document Type

Thesis

Divisions

science

Department

Department of Chemistry, Faculty of Science

Institution

University of Malaya

Abstract

Six iodoanilides incorporating different amide functionalities (e.g butyramide, furan carboxamide, cyclohexylamide, (2.1 to 2.6)) were prepared by established methods. These iodocarboxamides were transformed to the corresponding amido stilbenes (2.5 to 2.12) by an improved Heck procedure. Following silica gel chromatography, the resulting stilbene orthocarboxamides were exposed to diacetoxy iodobenzene with a view to indole synthesis.

Note

M.Sc. -- Jabatan Kimia, Fakulti Sains, Universiti Malaya, 2014.

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