3993-43-9Relevant articles and documents
A new route to pyranocoumarins and their benzannulated derivatives
Chattopadhyay, Shital K.,Mondal, Poulomi,Ghosh, Debalina
, p. 3331 - 3340 (2015/02/18)
A new protocol based on sequential applications of three atom-economic processes viz. Claisen rearrangement, olefin isomerisation, and ring-closing diene metathesis has been developed to access a range of linear and angularly fused pyranocoumarin derivatives. Incorporation of enyne (in place of diene) metathesis and Diels-Alder reaction in the sequence has allowed the corresponding benzannulated derivatives to be prepared in good yields.
DDQ Oxidation of 6- or 8-Allyl-7-hydroxycoumarins. A New Synthesis of Benzodipyrandiones and Furobenzopyranones
Prashant, Avula,Krupadanam, Gazula Levi David,Srimannarayana, Gutely
, p. 1191 - 1193 (2007/10/02)
A novel synthesis of 2H,8H-benzodipyran-2,8-diones, 2H,8H-benzodipyran-2,8-diones, 2H-furobenzopyran-2-ones, and 7H-furobenzopyran-7-ones was achieved by developing 2-pyrone and furan ring over coumarin. 6- or 8-Allyl-7-hydroxycoumarins on oxidation with 2,3-dichloro-5,6-dicyanobenzoquinone (DDQ) afforded benzodipyrandiones and furobenzopyranones.The structures of the compounds now synthesized were established by analytical, spectral, and comparison with authentic samples prepared by the known procedures.