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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Autor*in:	Alexander V. Aksenov [verfasserIn] Igor Yu. Grishin [verfasserIn] Nicolai A. Aksenov [verfasserIn] Vladimir V. Malyuga [verfasserIn] Dmitrii A. Aksenov [verfasserIn] Mezvah A. Nobi [verfasserIn] Michael Rubin [verfasserIn]

Format:	E-Artikel
Sprache:	Englisch

Erschienen:	2021

Schlagwörter:	nitroalkanes heterocyclic compounds quinozalines annulation

Übergeordnetes Werk:	In: Molecules - MDPI AG, 2003, 26(2021), 14, p 4274
Übergeordnetes Werk:	volume:26 ; year:2021 ; number:14, p 4274

Links:	Link aufrufen Link aufrufen Link aufrufen Journal toc

DOI / URN:	10.3390/molecules26144274

Katalog-ID:	DOAJ071979395

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520			\|a 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.
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allfieldsSound	10.3390/molecules26144274 doi (DE-627)DOAJ071979395 (DE-599)DOAJ09587f72118e41a7ac10e904cfb9b3d7 DE-627 ger DE-627 rakwb eng QD241-441 Alexander V. Aksenov verfasserin aut Electrophilically Activated Nitroalkanes in Synthesis of 3,4-Dihydroquinozalines 2021 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier 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. nitroalkanes heterocyclic compounds quinozalines annulation Organic chemistry Igor Yu. Grishin verfasserin aut Nicolai A. Aksenov verfasserin aut Vladimir V. Malyuga verfasserin aut Dmitrii A. Aksenov verfasserin aut Mezvah A. Nobi verfasserin aut Michael Rubin verfasserin aut In Molecules MDPI AG, 2003 26(2021), 14, p 4274 (DE-627)311313132 (DE-600)2008644-1 14203049 nnns volume:26 year:2021 number:14, p 4274 https://doi.org/10.3390/molecules26144274 kostenfrei https://doaj.org/article/09587f72118e41a7ac10e904cfb9b3d7 kostenfrei https://www.mdpi.com/1420-3049/26/14/4274 kostenfrei https://doaj.org/toc/1420-3049 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2005 GBV_ILN_2009 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2055 GBV_ILN_2111 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 26 2021 14, p 4274
language	English
source	In Molecules 26(2021), 14, p 4274 volume:26 year:2021 number:14, p 4274
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topic_facet	nitroalkanes heterocyclic compounds quinozalines annulation Organic chemistry
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authorswithroles_txt_mv	Alexander V. Aksenov @@aut@@ Igor Yu. Grishin @@aut@@ Nicolai A. Aksenov @@aut@@ Vladimir V. Malyuga @@aut@@ Dmitrii A. Aksenov @@aut@@ Mezvah A. Nobi @@aut@@ Michael Rubin @@aut@@
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callnumber-first	Q - Science
author	Alexander V. Aksenov
spellingShingle	Alexander V. Aksenov misc QD241-441 misc nitroalkanes misc heterocyclic compounds misc quinozalines misc annulation misc Organic chemistry Electrophilically Activated Nitroalkanes in Synthesis of 3,4-Dihydroquinozalines
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topic_title	QD241-441 Electrophilically Activated Nitroalkanes in Synthesis of 3,4-Dihydroquinozalines nitroalkanes heterocyclic compounds quinozalines annulation
topic	misc QD241-441 misc nitroalkanes misc heterocyclic compounds misc quinozalines misc annulation misc Organic chemistry
topic_unstemmed	misc QD241-441 misc nitroalkanes misc heterocyclic compounds misc quinozalines misc annulation misc Organic chemistry
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title	Electrophilically Activated Nitroalkanes in Synthesis of 3,4-Dihydroquinozalines
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title_full	Electrophilically Activated Nitroalkanes in Synthesis of 3,4-Dihydroquinozalines
author_sort	Alexander V. Aksenov
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author_browse	Alexander V. Aksenov Igor Yu. Grishin Nicolai A. Aksenov Vladimir V. Malyuga Dmitrii A. Aksenov Mezvah A. Nobi Michael Rubin
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title_sort	electrophilically activated nitroalkanes in synthesis of 3,4-dihydroquinozalines
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title_auth	Electrophilically Activated Nitroalkanes in Synthesis of 3,4-Dihydroquinozalines
abstract	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.
abstractGer	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.
abstract_unstemmed	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.
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container_issue	14, p 4274
title_short	Electrophilically Activated Nitroalkanes in Synthesis of 3,4-Dihydroquinozalines
url	https://doi.org/10.3390/molecules26144274 https://doaj.org/article/09587f72118e41a7ac10e904cfb9b3d7 https://www.mdpi.com/1420-3049/26/14/4274 https://doaj.org/toc/1420-3049
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Electrophilically Activated Nitroalkanes in Synthesis of 3,4-Dihydroquinozalines

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