75055-14-0Relevant articles and documents
An efficient synthesis of 3-(1H-tetrazol-5-yl)coumarins (=3-(1H-tetrazol-5-yl)-2H-1-benzopyran-2-ones) via domino knoevenagel condensation, Pinner reaction, and 1,3-dipolar cycloaddition in water
Tisseh, Zeinab Noroozi,Dabiri, Minoo,Bazgir, Ayoob
, p. 1600 - 1604 (2012/11/13)
A novel straightforward synthesis of 3-(1H-tetrazol-5-yl)coumarins (=3-(1H-tetrazol-5-yl)-2H-1-benzopyran-2-ones) 6 via domino Knoevenagel condensation, Pinner reaction, and 1,3-dipolar cycloaddition of substituted salicylaldehydes (=2-hydroxybenzaldehydes), malononitrile (propanedinitrile), and sodium azide in H2O is reported (Scheme1 and Table2). This general protocol provides a wide variety of 3-(1H-tetrazol-5-yl)coumarins in good yields under mild reaction conditions.
3-(Tetrazol-5-yl), 4-methyl-8-alkoxy coumarins and anti-allergic compositions thereof
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, (2008/06/13)
Coumarin derivatives of the general formula: STR1 wherein R is hydrogen atom, an alkyl group or an alkenyl group, R1 is hydrogen atom, an alkyl group, an alkenyl group or an alkoxy group, and the OR and R1 groups each are substituted at any of the 5, 6, 7 and 8 positions of the coumarin ring, and the salt thereof. The compounds are useful as antiallergic agent for preventing and treating allergic diseases.