Studies toward the total synthesis of glycinoeclepin A

Studies directed toward the synthesis of the A-ring portion of glycinoeclepin A are described. The enantioselective synthesis of key diketone intermediate 128 in four steps from 2,2-dimethyl-1,3-cyclohexanedione (5) has been accomplished via the acid-catalyzed intramolecular Michael cyclization of an enone generated in situ from 132. In the course of these studies, a new method for the preparation of the highly reactive a-alkynyl acroleins was developed. Several methods for the further elaborations of diketone 128 to the key enyne intermediate 95 were investigated and the best route developed to date involves the conversion of the methyl ketone to a vinyl triflate (177) followed by Sonogashira coupling. In addition, the conversion of diketone 128 to the vinyl halide 258 via a Shapiro strategy was achieved and model studies were carried out on the synthesis of vinylallene by coupling cuprate derivatives of this intermediate with propargyl alcohol derivatives.

Department dc:contributor.department

Massachusetts Institute of Technology. Dept. of Chemistry.

Grantor dc:publisher

Massachusetts Institute of Technology

Year dc:date.issued

2006

Author dc:creator

• Thongsornkleeb, Charnsak

Advisor dc:contributor.advisor

• Rick L. Danheiser.

• Chemistry.

Statement dc:rights

• M.I.T. theses are protected by copyright. They may be viewed from this source for any purpose, but reproduction or distribution in any format is prohibited without written permission. See provided URL for inquiries about permission.

Licence dc:rights.uri

• http://dspace.mit.edu/handle/1721.1/7582

Language dc:language.iso

eng

Handle dc:identifier.uri

http://hdl.handle.net/1721.1/34494

OAI identifier oai:identifier

oai:dspace.mit.edu:1721.1/34494