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Synthesis of Bi-, Ter-, and Quaterpyridinecarboxylates via Propargylisoxazole–Pyridine Rearrangement. / Galenko, Ekaterina E.; Kryukova, Mariya A.; Novikov, Mikhail S.; Khlebnikov, Alexander F.

в: The Journal of organic chemistry, Том 85, № 9, 01.05.2020, стр. 6109−6122.

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

Harvard

Galenko, EE, Kryukova, MA, Novikov, MS & Khlebnikov, AF 2020, 'Synthesis of Bi-, Ter-, and Quaterpyridinecarboxylates via Propargylisoxazole–Pyridine Rearrangement', The Journal of organic chemistry, Том. 85, № 9, стр. 6109−6122. https://doi.org/10.1021/acs.joc.0c00611

APA

Galenko, E. E., Kryukova, M. A., Novikov, M. S., & Khlebnikov, A. F. (2020). Synthesis of Bi-, Ter-, and Quaterpyridinecarboxylates via Propargylisoxazole–Pyridine Rearrangement. The Journal of organic chemistry, 85(9), 6109−6122. https://doi.org/10.1021/acs.joc.0c00611

Vancouver

Galenko EE, Kryukova MA, Novikov MS, Khlebnikov AF. Synthesis of Bi-, Ter-, and Quaterpyridinecarboxylates via Propargylisoxazole–Pyridine Rearrangement. The Journal of organic chemistry. 2020 Май 1;85(9):6109−6122. https://doi.org/10.1021/acs.joc.0c00611

Author

Galenko, Ekaterina E. ; Kryukova, Mariya A. ; Novikov, Mikhail S. ; Khlebnikov, Alexander F. / Synthesis of Bi-, Ter-, and Quaterpyridinecarboxylates via Propargylisoxazole–Pyridine Rearrangement. в: The Journal of organic chemistry. 2020 ; Том 85, № 9. стр. 6109−6122.

BibTeX

@article{69ee4031a3184b01826b18477287ef09,
title = "Synthesis of Bi-, Ter-, and Quaterpyridinecarboxylates via Propargylisoxazole–Pyridine Rearrangement",
abstract = "A flexible method was developed for the synthesis of2,2′-bi-, 2,2′:6′,2″-ter-, and 2,2′:6′,2′′:6′′,2‴-quaterpyridines con-taining a nicotinic acid moiety. The approach involves the Fe(II)/Au(I)-catalyzed rearrangement of key 4-propargylisoxazole build-ing blocks bearing a pyrid-2-yl or quinolin-2-yl substituent at the 3- position and Pd(0)-catalyzed cross-coupling reactions.",
author = "Galenko, {Ekaterina E.} and Kryukova, {Mariya A.} and Novikov, {Mikhail S.} and Khlebnikov, {Alexander F.}",
year = "2020",
month = may,
day = "1",
doi = "10.1021/acs.joc.0c00611",
language = "English",
volume = "85",
pages = "6109−6122",
journal = "Journal of Organic Chemistry",
issn = "0022-3263",
publisher = "American Chemical Society",
number = "9",

}

RIS

TY - JOUR

T1 - Synthesis of Bi-, Ter-, and Quaterpyridinecarboxylates via Propargylisoxazole–Pyridine Rearrangement

AU - Galenko, Ekaterina E.

AU - Kryukova, Mariya A.

AU - Novikov, Mikhail S.

AU - Khlebnikov, Alexander F.

PY - 2020/5/1

Y1 - 2020/5/1

N2 - A flexible method was developed for the synthesis of2,2′-bi-, 2,2′:6′,2″-ter-, and 2,2′:6′,2′′:6′′,2‴-quaterpyridines con-taining a nicotinic acid moiety. The approach involves the Fe(II)/Au(I)-catalyzed rearrangement of key 4-propargylisoxazole build-ing blocks bearing a pyrid-2-yl or quinolin-2-yl substituent at the 3- position and Pd(0)-catalyzed cross-coupling reactions.

AB - A flexible method was developed for the synthesis of2,2′-bi-, 2,2′:6′,2″-ter-, and 2,2′:6′,2′′:6′′,2‴-quaterpyridines con-taining a nicotinic acid moiety. The approach involves the Fe(II)/Au(I)-catalyzed rearrangement of key 4-propargylisoxazole build-ing blocks bearing a pyrid-2-yl or quinolin-2-yl substituent at the 3- position and Pd(0)-catalyzed cross-coupling reactions.

UR - http://www.scopus.com/inward/record.url?scp=85085120391&partnerID=8YFLogxK

U2 - 10.1021/acs.joc.0c00611

DO - 10.1021/acs.joc.0c00611

M3 - Article

VL - 85

SP - 6109−6122

JO - Journal of Organic Chemistry

JF - Journal of Organic Chemistry

SN - 0022-3263

IS - 9

ER -

ID: 53470308