Efficient synthesis of several methylene-expanded oxetanocin nucleoside analogues

Authors
Jung, ME Toyota, A
Citation
Me. Jung et A. Toyota, Efficient synthesis of several methylene-expanded oxetanocin nucleoside analogues, TETRAHEDR L, 41(19), 2000, pp. 3577-3581
Citations number
23
Categorie Soggetti
Chemistry & Analysis","Organic Chemistry/Polymer Science
Journal title
TETRAHEDRON LETTERS
ISSN journal
00404039 → ACNP
Volume
41
Issue
19
Year of publication
2000
Pages
3577 - 3581
Database
ISI
SICI code
0040-4039(20000506)41:19<3577:ESOSMO>2.0.ZU;2-I
Abstract
S-Glycidol 4 has been converted by a direct route via the dihydrofuran-3-me thanols 9ab into a series of methylene-expanded oxetanocin nucleoside analo gues, e.g., analogues of the normal nucleosides 2 and the known antiviral n ucleosides, AZT, FdT, and ddC, 3. (C) 2000 Elsevier Science Ltd. All rights reserved.