Aldol condensation reactions of tricarbonyliron complexes. Easy access to diastereomerically pure 1,2,3-trisubstituted 1,3-diols from alpha-substituted dienone complexes

Citation
M. Franck-neumann et al., Aldol condensation reactions of tricarbonyliron complexes. Easy access to diastereomerically pure 1,2,3-trisubstituted 1,3-diols from alpha-substituted dienone complexes, TETRAHEDR L, 41(21), 2000, pp. 4213-4217
Citations number
11
Categorie Soggetti
Chemistry & Analysis","Organic Chemistry/Polymer Science
Journal title
TETRAHEDRON LETTERS
ISSN journal
00404039 → ACNP
Volume
41
Issue
21
Year of publication
2000
Pages
4213 - 4217
Database
ISI
SICI code
0040-4039(20000529)41:21<4213:ACROTC>2.0.ZU;2-V
Abstract
Tricarbonyliron complexes of alpha-substituted dienones are well suited sta rting compounds for the synthesis of diastereomerically pure 1,2,3-trisubst ituted 1,3-diols of known configuration, among them 1,2,3-triols. This is a chieved by aldol condensation with an aldehyde, a reaction which gives one distinctly major isolated ketol, under Mukayiama conditions, followed by to tally stereoselective reduction. (C) 2000 Elsevier Science Ltd. All rights reserved.