Stereoselective sulfoxide directed reduction of 1,2-diketo-derivatives to enantiomerically pure syn and anti 1,2-diols. Correction of the relative configuration by X-ray and chemical correlation to goniobutenolides A and B.

Citation
G. Solladie et al., Stereoselective sulfoxide directed reduction of 1,2-diketo-derivatives to enantiomerically pure syn and anti 1,2-diols. Correction of the relative configuration by X-ray and chemical correlation to goniobutenolides A and B., TETRAHEDR L, 40(1), 1999, pp. 177-180
Citations number
6
Categorie Soggetti
Chemistry & Analysis","Organic Chemistry/Polymer Science
Journal title
TETRAHEDRON LETTERS
ISSN journal
00404039 → ACNP
Volume
40
Issue
1
Year of publication
1999
Pages
177 - 180
Database
ISI
SICI code
0040-4039(19990101)40:1<177:SSDRO1>2.0.ZU;2-J
Abstract
In our recent report on the enantioselective synthesis of syn and anti 1,2- diols from oxalyl-di-(N-methyl-N-methoxyamide), an unfortunate sample inver sion for C-13 NMR analysis led us to an incorrect attribution of their rela tive configurations. We report now the correction of the configurations of these diols by X-ray analysis and chemical correlation to two known natural products, goniobutenolides A and B. (C) 1998 Elsevier Science Ltd. All rig hts reserved.