The reactivity of thionaphtheno[3,2-b]pyrrole Full article
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Bulletin of the Academy of Sciences of the USSR Division of Chemical Science
ISSN: 0568-5230 |
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| Output data | Year: 1968, Volume: 17, Number: 1, Pages: 176-178 Pages count : 3 DOI: 10.1007/BF00914664 | ||
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Abstract:
By comparing the reactivity indices calculated by the molecular-orbit method, we conclude that in thionaphtheno[3,2-blpyrrole, electrophilic substitution must take place preferentially in position 2. © 1968 Consultants Bureau.
Cite:
Shkurko O.P.
The reactivity of thionaphtheno[3,2-b]pyrrole
Bulletin of the Academy of Sciences of the USSR Division of Chemical Science. 1968. V.17. N1. P.176-178. DOI: 10.1007/BF00914664 Scopus РИНЦ OpenAlex
The reactivity of thionaphtheno[3,2-b]pyrrole
Bulletin of the Academy of Sciences of the USSR Division of Chemical Science. 1968. V.17. N1. P.176-178. DOI: 10.1007/BF00914664 Scopus РИНЦ OpenAlex
Dates:
| Published print: | Jan 1, 1968 |
Identifiers:
| Scopus: | 2-s2.0-34250523025 |
| Elibrary: | 30914548 |
| OpenAlex: | W2003854775 |
Citing:
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