Publication:
Phosphorous Esters of 2,13-dihydroxy-7a, 14c-dihydronaphtho[1′,2′:4,5]furo [3,2-d] furan

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dc.contributor.authorsKizilcan N., Akar A., Talinli N., Yaşlak S.
dc.date.accessioned2022-03-15T01:53:48Z
dc.date.accessioned2026-01-11T16:30:30Z
dc.date.available2022-03-15T01:53:48Z
dc.date.issued1999
dc.description.abstract2,13-dihydroxy-7a, 14c-dihydronaphtho[1′,2′:4,5]furo[3.2-d]furan prepared from glyoxal bisulphite and 2,7-dihydroxynaphthalene was reacted with, C6H5PCl2, C6H5POCl2 and Br-C6H4OPOCl2 to produce its phosphorous esters. The structures of the products were investigated by MS, FTIR, 1H-NMR, 13C-NMR, and 31P-NMR. Although C6H5PCl2 gave a compound with a new ring containing phosphorous atom, C6H5POCl2 and Br-C6H4OPOCl2 resulted acyclic phosphorous esters.
dc.identifier.doi10.1515/HC.1999.5.1.27
dc.identifier.issn7930283
dc.identifier.urihttps://hdl.handle.net/11424/246403
dc.language.isoeng
dc.publisherFreund Publishing House Ltd
dc.relation.ispartofHeterocyclic Communications
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.titlePhosphorous Esters of 2,13-dihydroxy-7a, 14c-dihydronaphtho[1′,2′:4,5]furo [3,2-d] furan
dc.typearticle
dspace.entity.typePublication
oaire.citation.endPage30
oaire.citation.issue1
oaire.citation.startPage27
oaire.citation.titleHeterocyclic Communications
oaire.citation.volume5

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