A Facile and Expeditious Microwave‐Assisted Synthesis of Furo[3,4‐ b ]indeno[2,1‐ f ]quinolin‐1‐one Derivatives  via   Multicomponent Reaction | Zendy

Peng JuHua | Zendy; Jia RunHong | Zendy; Ma Ning | Zendy; Zhang Ge | Zendy; Wu FeiYue | Zendy; Cheng Chuang | Zendy; Tu ShuJiang | Zendy

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A Facile and Expeditious Microwave‐Assisted Synthesis of Furo[3,4‐ b ]indeno[2,1‐ f ]quinolin‐1‐one Derivatives via Multicomponent Reaction

Author(s) -

Peng JuHua,

Jia RunHong,

Ma Ning,

Zhang Ge,

Wu FeiYue,

Cheng Chuang,

Tu ShuJiang

Publication year - 2013

Publication title -

journal of heterocyclic chemistry

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 0.321

H-Index - 59

eISSN - 1943-5193

pISSN - 0022-152X

DOI - 10.1002/jhet.965

Subject(s) - chemistry , aldehyde , acetic acid , amine gas treating , yield (engineering) , microwave irradiation , condensation , solvent , condensation reaction , organic chemistry , microwave , combinatorial chemistry , catalysis , materials science , physics , quantum mechanics , metallurgy , thermodynamics

A series of furo[3,4‐ b ]indeno[2,1‐ f ]quinolin‐1‐one derivatives were synthesized by the condensation of an aromatic aldehyde with tetronic acid and 9 H ‐fluoren‐2‐amine in solvent of glacial acetic acid under microwave irradiation . This procedure offers several advantages including operational simplicity, clean reaction, and increased safety for small‐scale high‐speed synthesis.

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