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Reaction of 3,3,3-Tribromo- and 1,3,3,3-Tetrabromo-1-nitroprop-1-enes with Aliphatic Dienes Full article

Journal Russian Journal of General Chemistry
ISSN: 1070-3632 , E-ISSN: 1608-3350
Output data Year: 2020, Volume: 90, Number: 8, Pages: 1388-1397 Pages count : 10 DOI: 10.1134/S1070363220080022
Tags 1,4-addition; 3,3,3-tribromo-1-nitroprop-1-ene; cyclohexene derivatives; Diels–Alder reaction; hepta-1,5-diene
Authors Anisimova N.A. 1,2 , Slobodchikova E.K. 1 , Ivanova M.E. 3 , Rybalova T.V. 4,5
Affiliations
1 (Scopus) Herzen State Pedagogical University of Russia, St. Petersburg, 191186, Russian Federation
2 (Scopus) St. Petersburg State University of Industrial Technologies andDesign, St. Petersburg, 191186, Russian Federation
3 (Scopus) Altai State Agricultural University, Barnaul, 656049, Russian Federation
4 (Scopus) Vorozhtsov Novosibirsk Institute of Organic Chemistry, Siberian Branch,Russian Academy of Sciences, Novosibirsk, 630090, Russian Federation
5 (Scopus) Novosibirsk State University, Novosibirsk, 630090, Russian Federation

Abstract: Abstract: 3,3,3-Tribromo- and 1,3,3,3-tetrabromo-1-nitroprop-1-enes reacted with2-methyl- and 2,3-dimethylbuta-1,3-dienes to give cyclohexene, cyclohexane, andhepta-1,5-diene derivatives containing nitro and tribromomethyl groups. Theproducts were characterized by IR and 1H and13C NMR spectra and X-ray diffractiondata. © 2020, Pleiades Publishing, Ltd.
Cite: Anisimova N.A. , Slobodchikova E.K. , Ivanova M.E. , Rybalova T.V.
Reaction of 3,3,3-Tribromo- and 1,3,3,3-Tetrabromo-1-nitroprop-1-enes with Aliphatic Dienes
Russian Journal of General Chemistry. 2020. V.90. N8. P.1388-1397. DOI: 10.1134/S1070363220080022 WOS Scopus РИНЦ OpenAlex
Original: Анисимова Н.А. , Слободчикова Е.К. , Иванова М.Е. , Рыбалова Т.В.
ВЗАИМОДЕЙСТВИЕ 1-НИТРО-3,3,3-ТРИБРОМ- И 1-НИТРО-1,3,3,3-ТЕТРАБРОМПРОП-1-ЕНОВ С АЛИФАТИЧЕСКИМИ ДИЕНАМИ
Журнал общей химии (RUSS J GEN CHEM+). 2020. Т.90. №8. С.1173-1183. DOI: 10.31857/S0044460X2008003X РИНЦ OpenAlex
Dates:
Published print: Aug 1, 2020
Published online: Sep 15, 2020
Identifiers:
Web of science: WOS:000569346300002
Scopus: 2-s2.0-85091121712
Elibrary: 45350581
OpenAlex: W3169995397
Citing:
DB Citing
Scopus 1
Web of science 1
Elibrary 1
OpenAlex 1
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