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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 Full article

Journal Synthetic Communications
ISSN: 0039-7911 , E-ISSN: 1532-2432
Output data Year: 2019, Volume: 49, Number: 23, Pages: 3301-3310 Pages count : 10 DOI: 10.1080/00397911.2019.1661480
Tags Alkynes; Click chemistry; coumarin; heterocyclization; Sonogashira reaction
Authors Lipeeva Alla V. 1 , Shakirov Makhmut M. 1 , Shults Elvira E. 1,2
Affiliations
1 (Данные Web of science) Russian Acad Sci, Siberian Branch, Novosibirsk Inst Organ Chem, Med Chem Dept, Lavrentev Ave 9, Novosibirsk 630090, Russia
2 (Данные Web of science) Novosibirsk State Univ, Chem Dept, Novosibirsk, Russia

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.
Cite: Lipeeva A.V. , Shakirov M.M. , Shults E.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
Synthetic Communications. 2019. V.49. N23. P.3301-3310. DOI: 10.1080/00397911.2019.1661480 WOS Scopus РИНЦ OpenAlex
Dates:
Published online: Sep 13, 2019
Published print: Dec 2, 2019
Identifiers:
Web of science: WOS:000486553400001
Scopus: 2-s2.0-85074289643
Elibrary: 41667444
OpenAlex: W2973018959
Citing:
DB Citing
Web of science 3
Scopus 3
OpenAlex 3
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