Synthesis of carbocycles by enone-selective reduction using organoiodotin hydride

Citation
T. Suwa et al., Synthesis of carbocycles by enone-selective reduction using organoiodotin hydride, TETRAHEDR L, 41(18), 2000, pp. 3403-3406
Citations number
11
Categorie Soggetti
Chemistry & Analysis","Organic Chemistry/Polymer Science
Journal title
TETRAHEDRON LETTERS
ISSN journal
00404039 → ACNP
Volume
41
Issue
18
Year of publication
2000
Pages
3403 - 3406
Database
ISI
SICI code
0040-4039(20000429)41:18<3403:SOCBER>2.0.ZU;2-P
Abstract
By using di-n-butyliodotin hydride (n-Bu2SnIH), carbocycles were prepared f rom substrates hearing both enone and formyl moieties, where the enone-sele ctive reduction was followed by a diastereoselective intramolecular aldol r eaction. (C) 2000 Elsevier Science Ltd. All rights reserved.