Novel tandem "Ene-ISMS" methodology. Efficient and versatile assembly of apseudomonic acid C analogue.

Authors
Marko, IE Plancher, JM
Citation
Ie. Marko et Jm. Plancher, Novel tandem "Ene-ISMS" methodology. Efficient and versatile assembly of apseudomonic acid C analogue., TETRAHEDR L, 40(28), 1999, pp. 5259-5262
Citations number
33
Categorie Soggetti
Chemistry & Analysis","Organic Chemistry/Polymer Science
Journal title
TETRAHEDRON LETTERS
ISSN journal
00404039 → ACNP
Volume
40
Issue
28
Year of publication
1999
Pages
5259 - 5262
Database
ISI
SICI code
0040-4039(19990709)40:28<5259:NT"MEA>2.0.ZU;2-P
Abstract
The pseudomonic acid C analogue 19 can be readily constructed using a novel tandem methodology involving, as a key-step, an ene-reaction followed by a concomitant Intramolecular Silyl-Mediated Sakurai (ISMS) cyclisation. (C) 1999 Elsevier Science Ltd. All rights reserved.