Regioselectivity Of The Reactions Of Aryl Carbamoyl -N- Aryl Nitrile (mines With Some Dipolarophiles.

Mohamed Kamal Ahmad İbrahim

doi:10.1501/Commub_0000000224

EN

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

Details

Primary Language

English

Subjects

Chemical Engineering

Journal Section

Research Article

Authors

Mohamed Kamal Ahmad İbrahim This is me
Türkiye

Publication Date

January 1, 1983

Submission Date

January 1, 1983

Acceptance Date

-

Published in Issue

Year 1983 Volume: 29

DOI

https://doi.org/10.1501/Commub_0000000224

IZ

https://izlik.org/JA68GP88UX

Cite

RIS / Bibtex

APA

İbrahim, M. K. A. (1983). Regioselectivity Of The Reactions Of Aryl Carbamoyl -N- Aryl Nitrile (mines With Some Dipolarophiles. Communications Faculty of Sciences University of Ankara Series B Chemistry and Chemical Engineering, 29. https://doi.org/10.1501/Commub_0000000224

AMA

1.İbrahim MKA. Regioselectivity Of The Reactions Of Aryl Carbamoyl -N- Aryl Nitrile (mines With Some Dipolarophiles. Commun. Fac. Sci. Univ. Ank. Ser. B. 1983;29. doi:10.1501/Commub_0000000224

Chicago

İbrahim, Mohamed Kamal Ahmad. 1983. “Regioselectivity Of The Reactions Of Aryl Carbamoyl -N- Aryl Nitrile (mines With Some Dipolarophiles”. Communications Faculty of Sciences University of Ankara Series B Chemistry and Chemical Engineering 29 (January). https://doi.org/10.1501/Commub_0000000224.

EndNote

İbrahim MKA (January 1, 1983) Regioselectivity Of The Reactions Of Aryl Carbamoyl -N- Aryl Nitrile (mines With Some Dipolarophiles. Communications Faculty of Sciences University of Ankara Series B Chemistry and Chemical Engineering 29

IEEE

[1]M. K. A. İbrahim, “Regioselectivity Of The Reactions Of Aryl Carbamoyl -N- Aryl Nitrile (mines With Some Dipolarophiles”., Commun. Fac. Sci. Univ. Ank. Ser. B, vol. 29, Jan. 1983, doi: 10.1501/Commub_0000000224.

ISNAD

İbrahim, Mohamed Kamal Ahmad. “Regioselectivity Of The Reactions Of Aryl Carbamoyl -N- Aryl Nitrile (mines With Some Dipolarophiles”. Communications Faculty of Sciences University of Ankara Series B Chemistry and Chemical Engineering 29 (January 1, 1983). https://doi.org/10.1501/Commub_0000000224.

JAMA

1.İbrahim MKA. Regioselectivity Of The Reactions Of Aryl Carbamoyl -N- Aryl Nitrile (mines With Some Dipolarophiles. Commun. Fac. Sci. Univ. Ank. Ser. B. 1983;29. doi:10.1501/Commub_0000000224.

MLA

İbrahim, Mohamed Kamal Ahmad. “Regioselectivity Of The Reactions Of Aryl Carbamoyl -N- Aryl Nitrile (mines With Some Dipolarophiles”. Communications Faculty of Sciences University of Ankara Series B Chemistry and Chemical Engineering, vol. 29, Jan. 1983, doi:10.1501/Commub_0000000224.

Vancouver

1.Mohamed Kamal Ahmad İbrahim. Regioselectivity Of The Reactions Of Aryl Carbamoyl -N- Aryl Nitrile (mines With Some Dipolarophiles. Commun. Fac. Sci. Univ. Ank. Ser. B. 1983 Jan. 1;29. doi:10.1501/Commub_0000000224