Standard

Ugi reaction-derived 1H-pyrrol-2(5H)-ones proved as valid precursors to a new class of heterocyclic α-diazocarbonyl compounds. / Budeev, Anton; Kantin, Grigory; Dar'in, Dmitry; Krasavin, Mikhail.

In: Tetrahedron Letters, 14.12.2021.

Research output: Contribution to journal › Article › peer-review

Harvard

Budeev, A, Kantin, G, Dar'in, D & Krasavin, M 2021, 'Ugi reaction-derived 1H-pyrrol-2(5H)-ones proved as valid precursors to a new class of heterocyclic α-diazocarbonyl compounds', Tetrahedron Letters. https://doi.org/10.1016/j.tetlet.2021.153598

APA

Budeev, A., Kantin, G., Dar'in, D., & Krasavin, M. (2021). Ugi reaction-derived 1H-pyrrol-2(5H)-ones proved as valid precursors to a new class of heterocyclic α-diazocarbonyl compounds. Tetrahedron Letters, [153598]. https://doi.org/10.1016/j.tetlet.2021.153598

Vancouver

Budeev A, Kantin G, Dar'in D, Krasavin M. Ugi reaction-derived 1H-pyrrol-2(5H)-ones proved as valid precursors to a new class of heterocyclic α-diazocarbonyl compounds. Tetrahedron Letters. 2021 Dec 14. 153598. https://doi.org/10.1016/j.tetlet.2021.153598

Author

Budeev, Anton ; Kantin, Grigory ; Dar'in, Dmitry ; Krasavin, Mikhail. / Ugi reaction-derived 1H-pyrrol-2(5H)-ones proved as valid precursors to a new class of heterocyclic α-diazocarbonyl compounds. In: Tetrahedron Letters. 2021.

BibTeX

@article{aa233dd09b2d4f6183b723b25cfd5046,
title = "Ugi reaction-derived 1H-pyrrol-2(5H)-ones proved as valid precursors to a new class of heterocyclic α-diazocarbonyl compounds",
abstract = "1H-Pyrrol-2(5H)-ones synthesized via a modified literature procedure from primary amines, 3-substituted propiolic acids, isocyanides and glyoxal underwent a facile Regitz diazo transfer to give novel heterocyclic α-diazocarbonyl compounds – polysubstituted diazo pyrrol-2-ones.",
keywords = "1H-pyrrol-2(5H)-ones, Diazo transfer reaction, Heterocyclic α-diazocarbonyl compounds, Isocyanides, Multicomponent reaction",
author = "Anton Budeev and Grigory Kantin and Dmitry Dar'in and Mikhail Krasavin",
note = "Publisher Copyright: {\textcopyright} 2021 Elsevier Ltd",
year = "2021",
month = dec,
day = "14",
doi = "10.1016/j.tetlet.2021.153598",
language = "English",
journal = "Tetrahedron Letters",
issn = "0040-4039",
publisher = "Elsevier",

}

RIS

TY - JOUR

T1 - Ugi reaction-derived 1H-pyrrol-2(5H)-ones proved as valid precursors to a new class of heterocyclic α-diazocarbonyl compounds

AU - Budeev, Anton

AU - Kantin, Grigory

AU - Dar'in, Dmitry

AU - Krasavin, Mikhail

N1 - Publisher Copyright: © 2021 Elsevier Ltd

PY - 2021/12/14

Y1 - 2021/12/14

N2 - 1H-Pyrrol-2(5H)-ones synthesized via a modified literature procedure from primary amines, 3-substituted propiolic acids, isocyanides and glyoxal underwent a facile Regitz diazo transfer to give novel heterocyclic α-diazocarbonyl compounds – polysubstituted diazo pyrrol-2-ones.

AB - 1H-Pyrrol-2(5H)-ones synthesized via a modified literature procedure from primary amines, 3-substituted propiolic acids, isocyanides and glyoxal underwent a facile Regitz diazo transfer to give novel heterocyclic α-diazocarbonyl compounds – polysubstituted diazo pyrrol-2-ones.

KW - 1H-pyrrol-2(5H)-ones

KW - Diazo transfer reaction

KW - Heterocyclic α-diazocarbonyl compounds

KW - Isocyanides

KW - Multicomponent reaction

UR - http://www.scopus.com/inward/record.url?scp=85121384112&partnerID=8YFLogxK

U2 - 10.1016/j.tetlet.2021.153598

DO - 10.1016/j.tetlet.2021.153598

M3 - Article

AN - SCOPUS:85121384112

JO - Tetrahedron Letters

JF - Tetrahedron Letters

SN - 0040-4039

M1 - 153598

ER -

ID: 90454325