Abstract
2,13-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.
Original language | English |
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Pages (from-to) | 27-30 |
Number of pages | 4 |
Journal | Heterocyclic Communications |
Volume | 5 |
Issue number | 1 |
DOIs | |
Publication status | Published - 1999 |
Funding
This work was supported by the I.T.Ü Research Foundation.
Funders | Funder number |
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I.T.Ü Research Foundation |