PREPARATION AND STERIC STRUCTURES OF SATURATED OR PARTIALLY SATURATEDCYCLOPENTANE[B]PYRROLO[1,2-A][3,1]BENZOXAZINE AND CYCLOHEXANE[B]PYRROLO[1,2-A][3,1]BENZOXAZINE ISOMERS [1]
M. Virag et al., PREPARATION AND STERIC STRUCTURES OF SATURATED OR PARTIALLY SATURATEDCYCLOPENTANE[B]PYRROLO[1,2-A][3,1]BENZOXAZINE AND CYCLOHEXANE[B]PYRROLO[1,2-A][3,1]BENZOXAZINE ISOMERS [1], Journal of molecular structure, 440(1-3), 1998, pp. 147-154
The reactions of 2-ethoxycarbonylmethyleyclopentanone (1) with cis-(3a
) and trans-2-hydroxymethylcyclohex-4-enyl-1-amine (3b) and of 2-ethox
ycarbonylmethylcyclohexanone (2) with stereoisomeric 2-hydroxymethyl-1
-cyclohexylamines (4a,b) yield the isomeric cyclopentane-(5a,b) and cy
clohexane[b] pyrrolo[1,2-a][3,1]benzoxazinones (6a,b) with unsaturated
(5) or saturated (6) ring A, The steric structures were elucidated by
means H-1, C-13 NMR and X-ray measurements. (C) 1998 Elsevier Science
B.V.