Cookies on this website

We use cookies to ensure that we give you the best experience on our website. If you click 'Accept all cookies' we'll assume that you are happy to receive all cookies and you won't see this message again. If you click 'Reject all non-essential cookies' only necessary cookies providing core functionality such as security, network management, and accessibility will be enabled. Click 'Find out more' for information on how to change your cookie settings.

Conformational equilibrium isotope effects for hydrogen in cyclohexanones and other ketones are consistent with (i) hyperconjugation, (ii) analogues of hyperconjugation, and (iii) a difference in polarity between C-H and C-D bonds; steric effects are relatively unimportant. © 1989.

Original publication

DOI

10.1016/S0040-4039(01)80752-8

Type

Journal article

Journal

Tetrahedron Letters

Publication Date

01/01/1989

Volume

30

Pages

4589 - 4592