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New applications of pyridinium ylides toward heterocyclic synthesis. / Funt, Liya D.; Novikov, Mikhail S.; Khlebnikov, Alexander F.

в: Tetrahedron, Том 76, № 35, 131415, 28.08.2020.

Результаты исследований: Научные публикации в периодических изданияхОбзорная статьяРецензирование

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@article{97f8d90af3c84d7abb1dd45791f468e9,
title = "New applications of pyridinium ylides toward heterocyclic synthesis",
abstract = "The recent advances in the syntheses of various heterocycles based on pyridinium ylides are described. Depending on the reactivity of the pyridinium ylides and the reactants, a significant structural diversity of heterocycles can be prepared. It is evident that the application of pyridinium ylides is the most pertinent for the preparation of fused and spiropyrrole derivatives. Besides, often they are convenient precursors for the preparation of certain substituted non-fused pyrroles, furans, cyclopropanes and polyheterocycles. Particular attention is paid to heterocyclic syntheses involving the in situ formation of ylide precursors and their reaction partners under the multicomponent reaction conditions. The present survey covers studies published for the period from 2012 until the May 2020.",
keywords = "Furan, Heterocycles, Indolizine, Pyridine, Pyridinium ylide, Pyrrole, DOMINO REACTION, ONE-POT SYNTHESIS, EFFICIENT SYNTHESIS, IODINE-PROMOTED SYNTHESIS, SALTS, DIASTEREOSELECTIVE SYNTHESIS, FUNCTIONALIZED INDOLIZINES, 1,3-DIPOLAR CYCLOADDITION, DERIVATIVES, N-YLIDES",
author = "Funt, {Liya D.} and Novikov, {Mikhail S.} and Khlebnikov, {Alexander F.}",
year = "2020",
month = aug,
day = "28",
doi = "10.1016/j.tet.2020.131415",
language = "English",
volume = "76",
journal = "Tetrahedron",
issn = "0040-4020",
publisher = "Elsevier",
number = "35",

}

RIS

TY - JOUR

T1 - New applications of pyridinium ylides toward heterocyclic synthesis

AU - Funt, Liya D.

AU - Novikov, Mikhail S.

AU - Khlebnikov, Alexander F.

PY - 2020/8/28

Y1 - 2020/8/28

N2 - The recent advances in the syntheses of various heterocycles based on pyridinium ylides are described. Depending on the reactivity of the pyridinium ylides and the reactants, a significant structural diversity of heterocycles can be prepared. It is evident that the application of pyridinium ylides is the most pertinent for the preparation of fused and spiropyrrole derivatives. Besides, often they are convenient precursors for the preparation of certain substituted non-fused pyrroles, furans, cyclopropanes and polyheterocycles. Particular attention is paid to heterocyclic syntheses involving the in situ formation of ylide precursors and their reaction partners under the multicomponent reaction conditions. The present survey covers studies published for the period from 2012 until the May 2020.

AB - The recent advances in the syntheses of various heterocycles based on pyridinium ylides are described. Depending on the reactivity of the pyridinium ylides and the reactants, a significant structural diversity of heterocycles can be prepared. It is evident that the application of pyridinium ylides is the most pertinent for the preparation of fused and spiropyrrole derivatives. Besides, often they are convenient precursors for the preparation of certain substituted non-fused pyrroles, furans, cyclopropanes and polyheterocycles. Particular attention is paid to heterocyclic syntheses involving the in situ formation of ylide precursors and their reaction partners under the multicomponent reaction conditions. The present survey covers studies published for the period from 2012 until the May 2020.

KW - Furan

KW - Heterocycles

KW - Indolizine

KW - Pyridine

KW - Pyridinium ylide

KW - Pyrrole

KW - DOMINO REACTION

KW - ONE-POT SYNTHESIS

KW - EFFICIENT SYNTHESIS

KW - IODINE-PROMOTED SYNTHESIS

KW - SALTS

KW - DIASTEREOSELECTIVE SYNTHESIS

KW - FUNCTIONALIZED INDOLIZINES

KW - 1,3-DIPOLAR CYCLOADDITION

KW - DERIVATIVES

KW - N-YLIDES

UR - http://www.scopus.com/inward/record.url?scp=85088815763&partnerID=8YFLogxK

UR - https://www.mendeley.com/catalogue/08fe7651-3073-3953-931b-f308e5ffb352/

U2 - 10.1016/j.tet.2020.131415

DO - 10.1016/j.tet.2020.131415

M3 - Review article

AN - SCOPUS:85088815763

VL - 76

JO - Tetrahedron

JF - Tetrahedron

SN - 0040-4020

IS - 35

M1 - 131415

ER -

ID: 62157356