Ring closing metathesis in organic synthesis: Evolution of a high speed, solid phase method for the preparation of beta-turn mimetics.

Citation
Ad. Piscopio et al., Ring closing metathesis in organic synthesis: Evolution of a high speed, solid phase method for the preparation of beta-turn mimetics., TETRAHEDRON, 55(27), 1999, pp. 8189-8198
Citations number
60
Categorie Soggetti
Chemistry & Analysis","Organic Chemistry/Polymer Science
Journal title
TETRAHEDRON
ISSN journal
00404020 → ACNP
Volume
55
Issue
27
Year of publication
1999
Pages
8189 - 8198
Database
ISI
SICI code
0040-4020(19990702)55:27<8189:RCMIOS>2.0.ZU;2-9
Abstract
Complimentary solid phase syntheses of the Freidinger lactam class of p-tur n mimetics have been developed using ring closing metathesis as both the ke y carbon-carbon bond forming step and the cyclative cleavage mechanism. Sol id phase variants of the Fukuyama-Mitsunobu process were utilized as pad of a rapid three-step sequence to construct immobilized lactam precursors, an alternative solid phase process is offered which utilizes an Ugi/ring clos ing metathesis reaction tandem to deliver the desired compounds in two synt hetic operations. (C) 1999 Published by Elsevier Science Ltd, All rights re served.