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Regio- and stereoselective synthesis of nitrofunctionalized 1,2-oxazolidine analogs of nicotine
Authors:
- Agnieszka Fryźlewicz,
- Agnieszka Łapczuk-Krygier,
- Karolina Kula,
- Oleg M. Demchuk,
- Ewa Dresler,
- Radomir Jasiński
Abstract
(E)-3,3,3-Trichloro-1-nitroprop-1-ene undergoes [3+2] cycloaddition reaction with N-aryl(pyridin-3-yl) nitrones under mild conditions. The reaction is fully regio- and stereoselective and gives expected nitro-substituted nicotine analogs with 3,4-cis-4,5-trans-stereoconfiguration.
- Record ID
- CUT2709a528a72e4b9fb6cad956158438ce
- Publication categories
- ;
- Author
- Journal series
- Chemistry of Heterocyclic Compounds, ISSN 0009-3122, e-ISSN 1573-8353, Monthly
- Issue year
- 2020
- Vol
- 56
- No
- 1
- Pages
- 120-122
- Other elements of collation
- schem.; Bibliografia (na s.) - 122; Bibliografia (liczba pozycji) - 35; Oznaczenie streszczenia - Streszcz. ang.; Numeracja w czasopiśmie - Vol. 56, Iss. 1
- Keywords in English
- nicotine analogs, nitroalkenes, nitrones, 1,2-oxazolidines, [3+2] cycloaddition
- DOI
- DOI:10.1007/s10593-020-02631-6 Opening in a new tab
- URL
- https://link.springer.com/article/10.1007/s10593-020-02631-6 Opening in a new tab
- Language
- eng (en) English
- Score (nominal)
- 70
- Publication indicators
- Citation count
- 23
- Additional fields
- Indeksowana w: Web of Science, Scopus
- Uniform Resource Identifier
- https://cris.pk.edu.pl/info/article/CUT2709a528a72e4b9fb6cad956158438ce/
- URN
urn:pkr-prod:CUT2709a528a72e4b9fb6cad956158438ce
* presented citation count is obtained through Internet information analysis, and it is close to the number calculated by the Publish or PerishOpening in a new tab system.