Email this article Novel reaction of sulfonyl azides with fosphine sulfides
- Authors: Filimonov V.O1, Ilkin V.G1, Seliverstova E.A1, Bakulev V.A1
-
Affiliations:
- Ural Federal University
- Issue: Vol 59, No 5 (2023)
- Pages: 687-690
- Section: Articles
- URL: https://journals.rcsi.science/0514-7492/article/view/145091
- DOI: https://doi.org/10.31857/S0514749223050178
- EDN: https://elibrary.ru/EDCLLG
- ID: 145091
Cite item
Open Access
Access granted
Subscription Access
Abstract
(4-Methoxyphenyl)di(pyrrolidin-1-yl)phosphine sulfides were synthesized by reaction of Lausson’s reagent with cyclic amines. It was shown for the first time that phosphine sulfides react with aryl sulfonylazides when boiled in 1,4-dioxane with the elimination of nitrogen and elemental sulfur molecules and the formation of previously undescribed dicycloaminophosphoranylidene sulfonamides.
About the authors
V. O Filimonov
Ural Federal University
Email: v.a.bakulev@urfu.ru
V. G Ilkin
Ural Federal University
Email: v.a.bakulev@urfu.ru
E. A Seliverstova
Ural Federal University
Email: v.a.bakulev@urfu.ru
V. A Bakulev
Ural Federal University
Email: v.a.bakulev@urfu.ru
References
- Galieva N.A., Saveliev D.A., Eltsov O.S., Bakulev V.A., Lubec G., Xing J., Fan Z., Beryozkina T.V. Mendeleev Commun. 2021, 31, 495-497. doi: 10.1016/j.mencom.2021.07.019
- Ilkin V., Berseneva V., Beryozkina T., Glukhareva T., Dianova L., Dehaen W., Seliverstova E., Bakulev V. Beilstein J. Org. Chem. 2020, 16, 2937-2947. doi: 10.3762/bjoc.16.243
- Rupakova N.A., Bakulev V.A., Knippschild U., García-Reyes B., Eltsov O.S., Slesarev G.P., Beliaev N., Slepukhin P.A., Witt L., Peifer C., Beryozkina T.V. Arkivoc. 2017, 2017, 225-240. doi: 10.24820/ark.5550190.p010.200
- Aswad M., Chiba J., Tomohiro T., Hatanaka Y. Chem. Commun. 2013, 49, 10242-10244. doi: 10.1039/C3CC46055J
- Aswad M., Chiba J., Hatanaka Y., Tomohiro T. Tetrahedron Lett. 2019, 24, 1611-1613. doi: 10.1016/j.tetlet.2019.05.029
- Dianova L., Berseneva V., Beryozkina T., Efimov I., Kosterina M., Eltsov O., Dehaen W., Bakulev V. Eur. J. Org. Chem. 2015, 6917-6923. doi: 10.1002/ejoc.201500968
- Илькин В.Г., Берсенева В.С., Слепухин П.А., Бакулев В.А. ХГС. 2018, 54, 1153-1160.
- Il'kin V.G., Berseneva V.S., Slepukhin P.A., Bakulev V.A. Chem. Heterocycl. Compd. 2018, 54, 1153-1160. doi: 10.1007/s10593-019-02407-7
- Beryozkina T., Bakulev V., Dianova L., Berseneva V., Slepukhin P., Leban J., Kalaba P., Aher N.Y., Ilic M., Sitte H.H., Lubec G. Synthesis. 2016, 48, 1046-1054. doi: 10.1055/s-0035-1561350
