New Frontiers in Nitramine Reactivity via the Mitsunobu Reaction

New Frontiers in Nitramine Reactivity via the Mitsunobu Reaction Full article

Journal

Journal of Organic Chemistry
ISSN: 1520-6904 , E-ISSN: 0022-3263

Output data

Year: 2025, Volume: 90, Number: 1, Pages: 317–322 Pages count : DOI: 10.1021/acs.joc.4c02261

Authors

Sheremetev Aleksei B. ¹ , Gribov Pavel S. ¹ , Chernyshov Daniil A. ¹ , Lipilin Dmitry L. ¹ , Suponitsky Kyrill Yu. ¹

Affiliations

1	Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Moscow 119991, Russia

N-Nitro derivatives of primary alkyl, aryl and heteroarylamines can be directly alkylated with functionalized alcohols under Mitsunobu conditions at the N and/or O atoms of the nitramino moiety to give secondary nitramines or 1-alkoxydiazene 1-oxides, respectively.

Sheremetev A.B. , Gribov P.S. , Chernyshov D.A. , Lipilin D.L. , Suponitsky K.Y.
New Frontiers in Nitramine Reactivity via the Mitsunobu Reaction
Journal of Organic Chemistry. 2025. V.90. N1. P.317–322. DOI: 10.1021/acs.joc.4c02261 WOS Scopus OpenAlex

Web of science:	WOS:001380384800001
Scopus:	2-s2.0-85212632450
OpenAlex:	W4405620440

DB	Citing
OpenAlex	2
Web of science	1
Scopus	1