Conformational analysis and steric effects of substituents in derivatives of 3-oxo-, 3-imino-, and 3-methylenecyclohexene

1997 ◽  
Vol 46 (11) ◽  
pp. 1891-1896
Author(s):  
O. V. Shishkin ◽  
E. V. Solomovich ◽  
M. Yu. Antipin ◽  
A. S. Petrenko ◽  
L. A. Kutulya
1983 ◽  
Vol 61 (1) ◽  
pp. 109-115 ◽  
Author(s):  
R. St-Amour ◽  
M. St-Jacques

The conformational properties of 2-alkyl (Me, Et, i-Pr, and t-Bu) and 2-phenyl derivatives of 1,3-dioxa-5,6-benzocycloheptene (1) were studied by 13C dnmr. Analysis of slow exchange spectra at 100.6 MHz indicates that all derivatives except tert-butyl exist in an equilibrium of chair (major) and twist-boat (minor) conformations. Substituent effects on the position of the equilibrium are rationalized in terms of steric effects.


1974 ◽  
Vol 52 (24) ◽  
pp. 4062-4071 ◽  
Author(s):  
T. Bruce Grindley ◽  
Walter A. Szarek

The magnitude of —OCH2O— group geminal H,H coupling contants, the size of the vicinal coupling constants, and the tenets of conformational analysis were used to establish that in solution the conformation of the 1,3-dioxepane rings in derivatives of 1,3:2,5-di-O-methylenemannitol and 2,5-O-methylenemannitol is predominantly the twist-chair in which the C2 axis passes through the acetal carbon.


1983 ◽  
Vol 19 (3) ◽  
pp. 293-296 ◽  
Author(s):  
V. N. Zemlyanoi ◽  
I. L. Mushkalo ◽  
M. Yu. Kornilov ◽  
I. E. Boldeskul ◽  
M. L. Dekhtyar'

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