Modeling and experiment reveal an unexpected stereoelectronic effect on conformation and scalar couplings of alpha-aminoorganostannanes, with possible relevance to the tin-lithium exchange reaction
by Santiago, M.; Low, E.; Chambournier, G.; Gawley, R. E.
The solution conformation of N-methyl-2-(tributylstannyl)piperidines has been determined through the use of vicinal Sn-119-C-13 coupling constants, revealing a conformational distortion caused by an unexpected stereoelectronic effect in some cases. Specifically, the "equatorial" conformer is distorted into a half-chair, in which the nitrogen lone pair eclipses the C-Sn bond. This distortion, which "costs" approximately 1 kcal/mol, correlates with a conformational dependence of geminal Sn-119-N-15 couplings and a possible correlation with reactivity in the tin-lithium exchange reaction.
- Journal
- Journal of Organic Chemistry
- Volume
- 68
- Issue
- 22
- Year
- 2003
- Start Page
- 8480-8484
- URL
- https://dx.doi.org/10.1021/jo034948y
- ISBN/ISSN
- 1520-6904; 0022-3263
- DOI
- 10.1021/jo034948y