REACTION OF 3-PYRIDINE WITH SUBSTITUTED ACETOPHENONES

DOI: 10.1007/BF00472388

Source and publish data:

Chemistry of Heterocyclic Compounds p. 292 - 296 (1989)

Update date:2022-08-05

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Authors:

Kozlov, N.S.

Mikhalevskaya, S.V.

Serzhanina, V.A.

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Article abstract of DOI:10.1007/BF00472388

The reaction of 3-pyridine with substituted acetophenones in the presence of a proton catalyst leads to 1-aryl-3-(3-pyridyl)benzoquinolines.Noncyclic amino ketones - <1-aryl-3-(3-pyridyl)-3-(2-naphthylamino)>-1-propanones - precede the formation of the cyclic products.The IR, UV, PMR, and mass spectra of the synthesized compounds are discussed.

Full text of DOI:10.1007/BF00472388

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Article Doi

REACTION OF 3-PYRIDINE WITH SUBSTITUTED ACETOPHENONES

DOI: 10.1007/BF00472388

Source and publish data:

Authors:

Article abstract of DOI:10.1007/BF00472388

Full text of DOI:10.1007/BF00472388

Products guided by the article

R&D Labs maybe for 123216-32-0

Relevant to this article

Tributylphosphine-catalyzed stereoselective O-vinylation of 2-hydroxybenzaldehyde derivatives

Organization of spin- and redox-labile metal centers into Langmuir and Langmuir-Blodgett films

Improved enamine-type addition of dehydroaporphine using microwave irradiation

One-step synthesis of diarylpyrazolo[3,4- b]pyridines from isoflavones

Copper-catalyzed coupling reaction of c-ome bonds adjacent to a nitrogen atom with terminal alkynes

Donor-acceptor polymers based on multi-fused heptacyclic structures: Synthesis, characterization and photovoltaic applications