Standard

A facile approach to 6-amino-2H-pyrano[2,3-g]isoquinolin-2-ones via a sequential Sonogashira coupling of 6-cyanoumbelliferone triflate and annulations with amines. / Lipeeva, Alla V.; Shakirov, Makhmut M.; Shults, Elvira E.

в: Synthetic Communications, Том 49, № 23, 02.12.2019, стр. 3301-3310.

Результаты исследований: Научные публикации в периодических изданияхстатьяРецензирование

Harvard

APA

Vancouver

Lipeeva AV, Shakirov MM, Shults EE. A facile approach to 6-amino-2H-pyrano[2,3-g]isoquinolin-2-ones via a sequential Sonogashira coupling of 6-cyanoumbelliferone triflate and annulations with amines. Synthetic Communications. 2019 дек. 2;49(23):3301-3310. doi: 10.1080/00397911.2019.1661480

Author

Lipeeva, Alla V. ; Shakirov, Makhmut M. ; Shults, Elvira E. / A facile approach to 6-amino-2H-pyrano[2,3-g]isoquinolin-2-ones via a sequential Sonogashira coupling of 6-cyanoumbelliferone triflate and annulations with amines. в: Synthetic Communications. 2019 ; Том 49, № 23. стр. 3301-3310.

BibTeX

@article{bbb14c6765ed475dae59b312804741eb,
title = "A facile approach to 6-amino-2H-pyrano[2,3-g]isoquinolin-2-ones via a sequential Sonogashira coupling of 6-cyanoumbelliferone triflate and annulations with amines",
abstract = "Palladium-catalyzed synthesis of 2H-pyrano[2,3-g]isoquinolinones have been described from easily accessible precursor 6-cyanoumbelliferone triflate via sequential of Sonogashira coupling and the following annulations with several primary alkylamines under basic conditions The so obtained 6-propargylamino-2H-pyrano[2,3-g]isoquinolinones were involved in the CuAAC reaction with 2-azidobenzoic acid for obtaining 2H-pyrano[2,3-g]isoquinoline-benzoic acid hybrid compounds containing a 1,2,3-triazole linker.",
keywords = "Alkynes, Click chemistry, coumarin, heterocyclization, Sonogashira reaction",
author = "Lipeeva, {Alla V.} and Shakirov, {Makhmut M.} and Shults, {Elvira E.}",
year = "2019",
month = dec,
day = "2",
doi = "10.1080/00397911.2019.1661480",
language = "English",
volume = "49",
pages = "3301--3310",
journal = "Synthetic Communications",
issn = "0039-7911",
publisher = "Taylor and Francis Ltd.",
number = "23",

}

RIS

TY - JOUR

T1 - A facile approach to 6-amino-2H-pyrano[2,3-g]isoquinolin-2-ones via a sequential Sonogashira coupling of 6-cyanoumbelliferone triflate and annulations with amines

AU - Lipeeva, Alla V.

AU - Shakirov, Makhmut M.

AU - Shults, Elvira E.

PY - 2019/12/2

Y1 - 2019/12/2

N2 - Palladium-catalyzed synthesis of 2H-pyrano[2,3-g]isoquinolinones have been described from easily accessible precursor 6-cyanoumbelliferone triflate via sequential of Sonogashira coupling and the following annulations with several primary alkylamines under basic conditions The so obtained 6-propargylamino-2H-pyrano[2,3-g]isoquinolinones were involved in the CuAAC reaction with 2-azidobenzoic acid for obtaining 2H-pyrano[2,3-g]isoquinoline-benzoic acid hybrid compounds containing a 1,2,3-triazole linker.

AB - Palladium-catalyzed synthesis of 2H-pyrano[2,3-g]isoquinolinones have been described from easily accessible precursor 6-cyanoumbelliferone triflate via sequential of Sonogashira coupling and the following annulations with several primary alkylamines under basic conditions The so obtained 6-propargylamino-2H-pyrano[2,3-g]isoquinolinones were involved in the CuAAC reaction with 2-azidobenzoic acid for obtaining 2H-pyrano[2,3-g]isoquinoline-benzoic acid hybrid compounds containing a 1,2,3-triazole linker.

KW - Alkynes

KW - Click chemistry

KW - coumarin

KW - heterocyclization

KW - Sonogashira reaction

UR - http://www.scopus.com/inward/record.url?scp=85074289643&partnerID=8YFLogxK

U2 - 10.1080/00397911.2019.1661480

DO - 10.1080/00397911.2019.1661480

M3 - Article

AN - SCOPUS:85074289643

VL - 49

SP - 3301

EP - 3310

JO - Synthetic Communications

JF - Synthetic Communications

SN - 0039-7911

IS - 23

ER -

ID: 22088035