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