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Conformational study of N-vinyl-2-isopropyl- and N-vinyl-2-cyclopropylpyrroles by1H and13C NMR

✍ Scribed by A. V. Afonin; M. V. Sigalov; B. A. Trofimov; A. I. Mikhaleva; I. A. Aliev


Book ID
112448872
Publisher
Springer
Year
1991
Tongue
English
Weight
656 KB
Volume
40
Category
Article
ISSN
1573-9171

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Intramolecular interactions in N-vinyl-2
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## Abstract The introduction of a substituent in the 3‐position of the pyrrole ring in __N__‐vinyl‐2‐arylpyrroles and ‐2‐heteroarylpyrroles results in an increase in the dihedral angles between the planes of the pyrrole ring and the aryl (or heteroaryl) residue, and a decrease in the dihedral angle