Research Article
Regioselectivity Of The Reactions Of Aryl Carbamoyl -N- Aryl Nitrile (mines With Some Dipolarophiles.
Abstract
The regioselectivity of the cyloadditions of nitrile imines 1, derived from Aryl Carbamoyl hyd- razidoyl chlorides 2, to the C=C and C=S double bonds of the enol tautomer of benzoyl aceta- nilide, ethyl benzoylacetate, p-acetoacetotoluidide and the resonance stabilized thiocyanate anion respectively was investigated. The results indicate that the reactions studied are dipole- LUMO controlled and that the larger orbital coefficient in the LUMO of 1 is on the carbon atom.
Keywords
References
- Communications Faculty of Sciences University of Ankara Series B Chemistry and Chemical Engineering
Year 1983,
Volume: 29 , 0 - 0, 01.01.1983
Abstract
References
- Communications Faculty of Sciences University of Ankara Series B Chemistry and Chemical Engineering
There are 1 citations in total.
Details
| Primary Language | English |
|---|---|
| Subjects | Chemical Engineering |
| Journal Section | Research Article |
| Authors | |
| Publication Date | January 1, 1983 |
| DOI | https://doi.org/10.1501/Commub_0000000224 |
| IZ | https://izlik.org/JA68GP88UX |
| Published in Issue | Year 1983 Volume: 29 |
Communications Faculty of Sciences University of Ankara Series B Chemistry and Chemical Engineering
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