Reactions of 1-[(dimethylamino)methyl]naphthalen-2-ols with cyclic push-pull nitroenamines

[Figure not available: see fulltext.] A method was developed for the synthesis of 1-[2-nitro-2-(pyrrolidin-2-ylidene)ethyl]- and 1-[2-(imidazolidin-2-ylidene)-2-nitroethyl]-naphthalen-2-ols based on a reaction of 1,2-naphthoquinone-1-methide precursors with heterocyclic β-nitroenamines (pyrrolidine and imidazolidine derivatives). © 2018, Springer Science+Business Media, LLC, part of Springer Nature.

Authors
Lukashenko A.V.1 , Osipov D.V.1 , Osyanin V.A. 1, 2 , Klimochkin Y.N.1
Publisher
Латвийский институт органического синтеза Латвийской академии наук / Springer New York Consultants Bureau
Number of issue
12
Language
English
Pages
1369-1372
Status
Published
Volume
53
Year
2017
Organizations
  • 1 Samara State Technical University, 244 Molodogvardeiskaya St., Samara, 443100, Russian Federation
  • 2 RUDN University, 6 Miklukho-Maklaya St., Moscow, 117198, Russian Federation
Keywords
1-[2-(imidazolidin-2-ylidene)-2-nitroethyl]naphthalen-2-ols; 1-[2-nitro-2-(pyrrolidin-2-ylidene)ethyl]naphthalen-2-ols; Mannich bases; [4+2] cycloaddition; β-nitroenamines; о-quinone methides
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