Synthesis and conformational analysis of 2,6-dimethyl-1,5-diaza-cis-decalins

14Citations
Citations of this article
7Readers
Mendeley users who have this article in their library.
Get full text

Abstract

The stereoselective synthesis of 2,6-dimethyl-1,5-diaza-cis-decalins with the dimethyl groups syn or anti to the angular hydrogens has been accomplished starting from 1,5-diaza-cis-decalin. From an NMR study of the conformational properties of all three 2,6-dimethyl-1,5-diaza-cis-decalins, the components which affect the conformational equilibrium have been identified. © 2001 Elsevier Science Ltd.

Cite

CITATION STYLE

APA

Kozlowski, M. C., Xu, Z., & Santos, A. G. (2001). Synthesis and conformational analysis of 2,6-dimethyl-1,5-diaza-cis-decalins. Tetrahedron, 57(21), 4537–4542. https://doi.org/10.1016/S0040-4020(01)00370-2

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free