Electrophilically Activated Nitroalkanes in Synthesis of 3,4-Dihydroquinozalines

Nitroalkanes activated with polyphosphoric acid serve as efficient electrophiles in reactions with various nucleophilic amines. Strategically placed second functionality allows for the design of annulation reactions enabling preparation of various heterocycles. This strategy was employed to develop...

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Main Authors: Alexander V. Aksenov, Igor Yu. Grishin, Nicolai A. Aksenov, Vladimir V. Malyuga, Dmitrii A. Aksenov, Mezvah A. Nobi, Michael Rubin
Format: Article
Language:English
Published: MDPI AG 2021-07-01
Series:Molecules
Subjects:
Online Access:https://www.mdpi.com/1420-3049/26/14/4274
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spelling doaj-09587f72118e41a7ac10e904cfb9b3d72021-07-23T13:56:39ZengMDPI AGMolecules1420-30492021-07-01264274427410.3390/molecules26144274Electrophilically Activated Nitroalkanes in Synthesis of 3,4-DihydroquinozalinesAlexander V. Aksenov0Igor Yu. Grishin1Nicolai A. Aksenov2Vladimir V. Malyuga3Dmitrii A. Aksenov4Mezvah A. Nobi5Michael Rubin6Department of Chemistry, North Caucasus Federal University, 1a Pushkin St., 355017 Stavropol, RussiaDepartment of Chemistry, North Caucasus Federal University, 1a Pushkin St., 355017 Stavropol, RussiaDepartment of Chemistry, North Caucasus Federal University, 1a Pushkin St., 355017 Stavropol, RussiaDepartment of Chemistry, North Caucasus Federal University, 1a Pushkin St., 355017 Stavropol, RussiaDepartment of Chemistry, North Caucasus Federal University, 1a Pushkin St., 355017 Stavropol, RussiaDepartment of Chemistry, University of Kansas, 1567 Irving Hill Road, Lawrence, KS 66045, USADepartment of Chemistry, North Caucasus Federal University, 1a Pushkin St., 355017 Stavropol, RussiaNitroalkanes activated with polyphosphoric acid serve as efficient electrophiles in reactions with various nucleophilic amines. Strategically placed second functionality allows for the design of annulation reactions enabling preparation of various heterocycles. This strategy was employed to develop an innovative synthetic approach towards 3,4-dihydroquinazolines from readily available 2-(aminomethyl)anilines.https://www.mdpi.com/1420-3049/26/14/4274nitroalkanesheterocyclic compoundsquinozalinesannulation
collection DOAJ
language English
format Article
sources DOAJ
author Alexander V. Aksenov
Igor Yu. Grishin
Nicolai A. Aksenov
Vladimir V. Malyuga
Dmitrii A. Aksenov
Mezvah A. Nobi
Michael Rubin
spellingShingle Alexander V. Aksenov
Igor Yu. Grishin
Nicolai A. Aksenov
Vladimir V. Malyuga
Dmitrii A. Aksenov
Mezvah A. Nobi
Michael Rubin
Electrophilically Activated Nitroalkanes in Synthesis of 3,4-Dihydroquinozalines
Molecules
nitroalkanes
heterocyclic compounds
quinozalines
annulation
author_facet Alexander V. Aksenov
Igor Yu. Grishin
Nicolai A. Aksenov
Vladimir V. Malyuga
Dmitrii A. Aksenov
Mezvah A. Nobi
Michael Rubin
author_sort Alexander V. Aksenov
title Electrophilically Activated Nitroalkanes in Synthesis of 3,4-Dihydroquinozalines
title_short Electrophilically Activated Nitroalkanes in Synthesis of 3,4-Dihydroquinozalines
title_full Electrophilically Activated Nitroalkanes in Synthesis of 3,4-Dihydroquinozalines
title_fullStr Electrophilically Activated Nitroalkanes in Synthesis of 3,4-Dihydroquinozalines
title_full_unstemmed Electrophilically Activated Nitroalkanes in Synthesis of 3,4-Dihydroquinozalines
title_sort electrophilically activated nitroalkanes in synthesis of 3,4-dihydroquinozalines
publisher MDPI AG
series Molecules
issn 1420-3049
publishDate 2021-07-01
description Nitroalkanes activated with polyphosphoric acid serve as efficient electrophiles in reactions with various nucleophilic amines. Strategically placed second functionality allows for the design of annulation reactions enabling preparation of various heterocycles. This strategy was employed to develop an innovative synthetic approach towards 3,4-dihydroquinazolines from readily available 2-(aminomethyl)anilines.
topic nitroalkanes
heterocyclic compounds
quinozalines
annulation
url https://www.mdpi.com/1420-3049/26/14/4274
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