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Please use this identifier to cite or link to this item: https://scholarbank.nus.edu.sg/handle/10635/52781
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dc.titleAn improved method for the synthesis of 2-(p-halobenzyl)-3-aryl-6-methoxybenzofurans as selective ligands for the antiestrogen-binding sites
dc.contributor.authorNg, S.-C.
dc.contributor.authorKon, O.-L.
dc.contributor.authorSim, K.-Y.
dc.contributor.authorSrikanth, N.
dc.date.accessioned2014-05-19T02:49:58Z
dc.date.available2014-05-19T02:49:58Z
dc.date.issued1993
dc.identifier.citationNg, S.-C.,Kon, O.-L.,Sim, K.-Y.,Srikanth, N. (1993). An improved method for the synthesis of 2-(p-halobenzyl)-3-aryl-6-methoxybenzofurans as selective ligands for the antiestrogen-binding sites. Synthetic Communications 23 (13) : 1843-1853. ScholarBank@NUS Repository.
dc.identifier.issn00397911
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/52781
dc.description.abstractA series of 2-(p-fluorobenzyl)-3-aryl-6-methoxybenzofurans has been prepared in good yields in a two-step sequence from the corresponding benzylidencoumaranones (aurones).
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentCHEMISTRY
dc.contributor.departmentBIOCHEMISTRY
dc.description.sourcetitleSynthetic Communications
dc.description.volume23
dc.description.issue13
dc.description.page1843-1853
dc.description.codenSYNCA
dc.identifier.isiutNOT_IN_WOS
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