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Plant Coumarins : XVII. Synthesis and Transformations of 7-Hydroxy-2-oxo-2H-chromene-6-carboxamides. / Zakharov, D. O.; Lipeeva, A. V.; Gatilov, Yu V. и др.

в: Russian Journal of Organic Chemistry, Том 55, № 10, 9, 01.10.2019, стр. 1518-1526.

Результаты исследований: Научные публикации в периодических изданиях › статья › Рецензирование

Harvard

Zakharov, DO, Lipeeva, AV, Gatilov, YV, Makarov, AG & Shults, EE 2019, 'Plant Coumarins: XVII. Synthesis and Transformations of 7-Hydroxy-2-oxo-2H-chromene-6-carboxamides', Russian Journal of Organic Chemistry, Том. 55, № 10, 9, стр. 1518-1526. https://doi.org/10.1134/S1070428019100099

APA

Zakharov, D. O., Lipeeva, A. V., Gatilov, Y. V., Makarov, A. G., & Shults, E. E. (2019). Plant Coumarins: XVII. Synthesis and Transformations of 7-Hydroxy-2-oxo-2H-chromene-6-carboxamides. Russian Journal of Organic Chemistry, 55(10), 1518-1526. [9]. https://doi.org/10.1134/S1070428019100099

Vancouver

Zakharov DO, Lipeeva AV, Gatilov YV, Makarov AG, Shults EE. Plant Coumarins: XVII. Synthesis and Transformations of 7-Hydroxy-2-oxo-2H-chromene-6-carboxamides. Russian Journal of Organic Chemistry. 2019 окт. 1;55(10):1518-1526. 9. doi: 10.1134/S1070428019100099

Author

Zakharov, D. O. ; Lipeeva, A. V. ; Gatilov, Yu V. и др. / Plant Coumarins : XVII. Synthesis and Transformations of 7-Hydroxy-2-oxo-2H-chromene-6-carboxamides. в: Russian Journal of Organic Chemistry. 2019 ; Том 55, № 10. стр. 1518-1526.

BibTeX

@article{b775eaa6e30741e8918d72e2e16d7b36,
title = "Plant Coumarins: XVII. Synthesis and Transformations of 7-Hydroxy-2-oxo-2H-chromene-6-carboxamides",
abstract = "Umbelliferone-6-carbonyl chloride reacted with amines and α-, β-, and ω-amino acid methyl esters to afford the corresponding N-substituted 7-hydroxy-2-oxo-2H-chromene-6-carboxamides. The reaction of umbelliferone-6-carbonyl chloride with glycine gave 2-(7-hydroxy-2-oxo-2H-chromene-6-carboxamido)acetic acid which was converted into acid chloride, and the latter reacted with benzylamines and α-amino acid methyl esters to produce compounds containing a dipeptide fragment.",
keywords = "amides, amino acids, coumarins, peptides, umbelliferone",
author = "Zakharov, {D. O.} and Lipeeva, {A. V.} and Gatilov, {Yu V.} and Makarov, {A. G.} and Shults, {E. E.}",
note = "Funding Information: The authors thank the Joint Chemical Service Center, Siberian Branch, Russian Academy of Sciences for providing facilities for spectral and analytical studies. Funding Information: This study was performed under financial support by the Russian Foundation for Basic Research and by the Authorities of Novosibirsk oblast (project no. 18-43- 543 014).",
year = "2019",
month = oct,
day = "1",
doi = "10.1134/S1070428019100099",
language = "English",
volume = "55",
pages = "1518--1526",
journal = "Russian Journal of Organic Chemistry",
issn = "1070-4280",
publisher = "Maik Nauka-Interperiodica Publishing",
number = "10",

}

RIS

TY - JOUR

T1 - Plant Coumarins

T2 - XVII. Synthesis and Transformations of 7-Hydroxy-2-oxo-2H-chromene-6-carboxamides

AU - Zakharov, D. O.

AU - Lipeeva, A. V.

AU - Gatilov, Yu V.

AU - Makarov, A. G.

AU - Shults, E. E.

N1 - Funding Information: The authors thank the Joint Chemical Service Center, Siberian Branch, Russian Academy of Sciences for providing facilities for spectral and analytical studies. Funding Information: This study was performed under financial support by the Russian Foundation for Basic Research and by the Authorities of Novosibirsk oblast (project no. 18-43- 543 014).

PY - 2019/10/1

Y1 - 2019/10/1

N2 - Umbelliferone-6-carbonyl chloride reacted with amines and α-, β-, and ω-amino acid methyl esters to afford the corresponding N-substituted 7-hydroxy-2-oxo-2H-chromene-6-carboxamides. The reaction of umbelliferone-6-carbonyl chloride with glycine gave 2-(7-hydroxy-2-oxo-2H-chromene-6-carboxamido)acetic acid which was converted into acid chloride, and the latter reacted with benzylamines and α-amino acid methyl esters to produce compounds containing a dipeptide fragment.

AB - Umbelliferone-6-carbonyl chloride reacted with amines and α-, β-, and ω-amino acid methyl esters to afford the corresponding N-substituted 7-hydroxy-2-oxo-2H-chromene-6-carboxamides. The reaction of umbelliferone-6-carbonyl chloride with glycine gave 2-(7-hydroxy-2-oxo-2H-chromene-6-carboxamido)acetic acid which was converted into acid chloride, and the latter reacted with benzylamines and α-amino acid methyl esters to produce compounds containing a dipeptide fragment.

KW - amides

KW - amino acids

KW - coumarins

KW - peptides

KW - umbelliferone

UR - http://www.scopus.com/inward/record.url?scp=85076861428&partnerID=8YFLogxK

UR - https://www.elibrary.ru/item.asp?id=43227308

U2 - 10.1134/S1070428019100099

DO - 10.1134/S1070428019100099

M3 - Article

AN - SCOPUS:85076861428

VL - 55

SP - 1518

EP - 1526

JO - Russian Journal of Organic Chemistry

JF - Russian Journal of Organic Chemistry

SN - 1070-4280

IS - 10

M1 - 9

ER -

ID: 28277753