SYNTHESIS OF 2,5-DIHYDROFURANS VIA ALKYLIDENE CARBENE INSERTION REACTIONS

Authors
WALKER LF CONNOLLY S WILLS M
Citation
Lf. Walker et al., SYNTHESIS OF 2,5-DIHYDROFURANS VIA ALKYLIDENE CARBENE INSERTION REACTIONS, Tetrahedron letters, 39(29), 1998, pp. 5273-5276
Citations number
29
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
Tetrahedron letters → ACNP
ISSN journal
00404039
Volume
39
Issue
29
Year of publication
1998
Pages
5273 - 5276
Database
ISI
SICI code
0040-4039(1998)39:29<5273:SO2VAC>2.0.ZU;2-9
Abstract
The insertion of vinylidene carbenes into C-H bonds is an efficient me thod for the synthesis of 2,5-dihydrofurans. The methodology provides a convenient entry to the core structure of squalestatin/zaragozic aci d natural products. (C) 1998 Elsevier Science Ltd. All rights reserved .