INTRAMOLECULAR CYCLOADDITION OF 3-O-CYCLOHEXENYL CARBOHYDRATE NITRONES - DIASTEREOSELECTIVE SYNTHESIS OF OPTICALLY PURE TETRAHYDROPYRANO[2,3]CYCLOHEXANE DERIVATIVES

Citation
A. Bhattacharjee et al., INTRAMOLECULAR CYCLOADDITION OF 3-O-CYCLOHEXENYL CARBOHYDRATE NITRONES - DIASTEREOSELECTIVE SYNTHESIS OF OPTICALLY PURE TETRAHYDROPYRANO[2,3]CYCLOHEXANE DERIVATIVES, Tetrahedron letters, 37(42), 1996, pp. 7635-7636
Citations number
3
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
ISSN journal
00404039
Volume
37
Issue
42
Year of publication
1996
Pages
7635 - 7636
Database
ISI
SICI code
0040-4039(1996)37:42<7635:ICO3CN>2.0.ZU;2-Z
Abstract
The intramolecular cycloaddition of nitrones derived from 3-O-cyclohex enylfuranoside-5-aldehydes led to diastereoselective formation of tetr ahydropyrano[2, 3]cyclohexane ring systems with six chiral centres. Co pyright (C) 1996 Elsevier Science Ltd