4.3 Article

A concise metal-free synthesis of xanthene derivatives mediated by achiral 2-aminophenol under solvent-free conditions

Journal

SYNTHETIC COMMUNICATIONS
Volume 52, Issue 5, Pages 712-723

Publisher

TAYLOR & FRANCIS INC
DOI: 10.1080/00397911.2022.2047730

Keywords

Xanthene; multicomponent reaction; organo-catalyst; dimedone; beta-naphthol; 2-aminophenol; solvent-free

Funding

  1. UGC

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A green and efficient method for synthesizing biologically active xanthene derivatives has been developed using a three-component reaction mediated by 2-aminophenol. The method offers advantages such as short reaction time, easy product isolation, non-toxic catalyst, and metal-free process.
An efficient green technique has been developed for the synthesis of some biologically active 12-aryl or 12-alkyl 8,9,10,12-tetrahydrobenzo[a]xanthenes-11-one and 3,3,6,6-tetramethy1-3,4,5,6,7,9-hexahydro-1H-xanthene-1,8(2H)-dione derivatives have been described. This process arranged a three-component one-pot condensation of aldehydes, 2-naphthol, and dimedone mediated by 2-aminophenol and has offered an excellent scope of tailoring a large number of xanthene derivatives with good to charming yields. Short reaction time, straightforward, easy product isolation technique, non-toxic catalyst, and above all metal-free process are noteworthy advantages of this method. [GRAPHICS] .

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