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Functionalized buta-1,3-diynyl-N-methylpyrazoles by sequential “diacetylene zipper” and Sonogashira coupling reactions. / Govdi, Anastasiya I.; Kulyashova, Alexandra E.; Vasilevsky, Sergey F.; Balova, Irina A.

в: Tetrahedron Letters, Том 58, № 8, 2017, стр. 762-765.

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

Harvard

Govdi, AI, Kulyashova, AE, Vasilevsky, SF & Balova, IA 2017, 'Functionalized buta-1,3-diynyl-N-methylpyrazoles by sequential “diacetylene zipper” and Sonogashira coupling reactions', Tetrahedron Letters, Том. 58, № 8, стр. 762-765. https://doi.org/10.1016/j.tetlet.2017.01.032

APA

Govdi, A. I., Kulyashova, A. E., Vasilevsky, S. F., & Balova, I. A. (2017). Functionalized buta-1,3-diynyl-N-methylpyrazoles by sequential “diacetylene zipper” and Sonogashira coupling reactions. Tetrahedron Letters, 58(8), 762-765. https://doi.org/10.1016/j.tetlet.2017.01.032

Vancouver

Govdi AI, Kulyashova AE, Vasilevsky SF, Balova IA. Functionalized buta-1,3-diynyl-N-methylpyrazoles by sequential “diacetylene zipper” and Sonogashira coupling reactions. Tetrahedron Letters. 2017;58(8):762-765. https://doi.org/10.1016/j.tetlet.2017.01.032

Author

Govdi, Anastasiya I. ; Kulyashova, Alexandra E. ; Vasilevsky, Sergey F. ; Balova, Irina A. / Functionalized buta-1,3-diynyl-N-methylpyrazoles by sequential “diacetylene zipper” and Sonogashira coupling reactions. в: Tetrahedron Letters. 2017 ; Том 58, № 8. стр. 762-765.

BibTeX

@article{0bb77c14beba466098ceafb26bc25a5c,
title = "Functionalized buta-1,3-diynyl-N-methylpyrazoles by sequential “diacetylene zipper” and Sonogashira coupling reactions",
abstract = "A reaction sequence consisting of the “Diacetylene zipper” of buta-1,3-diynes from internal to terminal isomers, followed by Sonogashira cross-coupling with 3-,4- or 5-iodopyrazoles, was investigated as a new approach to buta-1,3-diynyl-N-methylpyrazoles. Various pyrazoles bearing alkyl and hydroxyalkyl containing buta-1,3-diyne substituents in the 3-,4- or 5-position and functional groups at the neighboring positions of the ring were obtained.",
keywords = "Buta-1,3-diynes, Diacetylene zipper, Pyrazoles, Sonogashira cross-coupling",
author = "Govdi, {Anastasiya I.} and Kulyashova, {Alexandra E.} and Vasilevsky, {Sergey F.} and Balova, {Irina A.}",
note = "Publisher Copyright: {\textcopyright} 2017 Elsevier Ltd",
year = "2017",
doi = "10.1016/j.tetlet.2017.01.032",
language = "English",
volume = "58",
pages = "762--765",
journal = "Tetrahedron Letters",
issn = "0040-4039",
publisher = "Elsevier",
number = "8",

}

RIS

TY - JOUR

T1 - Functionalized buta-1,3-diynyl-N-methylpyrazoles by sequential “diacetylene zipper” and Sonogashira coupling reactions

AU - Govdi, Anastasiya I.

AU - Kulyashova, Alexandra E.

AU - Vasilevsky, Sergey F.

AU - Balova, Irina A.

N1 - Publisher Copyright: © 2017 Elsevier Ltd

PY - 2017

Y1 - 2017

N2 - A reaction sequence consisting of the “Diacetylene zipper” of buta-1,3-diynes from internal to terminal isomers, followed by Sonogashira cross-coupling with 3-,4- or 5-iodopyrazoles, was investigated as a new approach to buta-1,3-diynyl-N-methylpyrazoles. Various pyrazoles bearing alkyl and hydroxyalkyl containing buta-1,3-diyne substituents in the 3-,4- or 5-position and functional groups at the neighboring positions of the ring were obtained.

AB - A reaction sequence consisting of the “Diacetylene zipper” of buta-1,3-diynes from internal to terminal isomers, followed by Sonogashira cross-coupling with 3-,4- or 5-iodopyrazoles, was investigated as a new approach to buta-1,3-diynyl-N-methylpyrazoles. Various pyrazoles bearing alkyl and hydroxyalkyl containing buta-1,3-diyne substituents in the 3-,4- or 5-position and functional groups at the neighboring positions of the ring were obtained.

KW - Buta-1,3-diynes

KW - Diacetylene zipper

KW - Pyrazoles

KW - Sonogashira cross-coupling

UR - http://www.scopus.com/inward/record.url?scp=85009796972&partnerID=8YFLogxK

U2 - 10.1016/j.tetlet.2017.01.032

DO - 10.1016/j.tetlet.2017.01.032

M3 - Article

AN - SCOPUS:85009796972

VL - 58

SP - 762

EP - 765

JO - Tetrahedron Letters

JF - Tetrahedron Letters

SN - 0040-4039

IS - 8

ER -

ID: 97811640