| dc.contributor.author | OYMAN, U | |
| dc.contributor.author | GUNAYDIN, K | |
| dc.date.accessioned | 2021-03-03T08:26:03Z | |
| dc.date.available | 2021-03-03T08:26:03Z | |
| dc.date.issued | 1994 | |
| dc.identifier.citation | OYMAN U., GUNAYDIN K., "CONDENSATION OF ETHYL ACETOACETATE WITH NAPHTHALENE-DIOLS - THE SYNTHESIS OF SOME NOVEL COUMARINS AND CHROMONES .1.", BULLETIN DES SOCIETES CHIMIQUES BELGES, cilt.103, sa.12, ss.763-764, 1994 | |
| dc.identifier.issn | 0037-9646 | |
| dc.identifier.other | vv_1032021 | |
| dc.identifier.other | av_1772ca32-59f9-4196-af3a-50793d4bbcd5 | |
| dc.identifier.uri | http://hdl.handle.net/20.500.12627/21127 | |
| dc.identifier.uri | http://apps.webofknowledge.com/full_record.do?product=UA&search_mode=Refine&qid=3&SID=V2uJhu7LKQODlQgLfv2&page=1&doc=6 | |
| dc.identifier.uri | https://doi.org/10.1002/bscb.19941031208 | |
| dc.description.abstract | In Simonis reaction with ethyl acetoacetate naphthalene-2,6-diol gives 8-hydroxy-3-methyl-1 H-naphtho[2,1-b]pyran-l-one and naphthalene-2,7-diol gives the related 9-hydroxy isomer. In Pechman reactions, the former diet yields a coumarin, 8-hydroxy-1-methyl-3H-naphtho[2,1-b]-pyran-3-one, with the corresponding orientation, but the latter diol gives a coumarin, 8-hydroxy-4-methyl-2H-naphtho[2,3-b]-pyran-2-one, with an unusual linear annelation pattern. | |
| dc.language.iso | eng | |
| dc.subject | Alkoloidler | |
| dc.subject | KİMYA, MULTİDİSİPLİNER | |
| dc.subject | Kimya | |
| dc.subject | Temel Bilimler (SCI) | |
| dc.subject | Biyokimya | |
| dc.subject | Temel Bilimler | |
| dc.title | CONDENSATION OF ETHYL ACETOACETATE WITH NAPHTHALENE-DIOLS - THE SYNTHESIS OF SOME NOVEL COUMARINS AND CHROMONES .1. | |
| dc.type | Makale | |
| dc.relation.journal | BULLETIN DES SOCIETES CHIMIQUES BELGES | |
| dc.contributor.department | , , | |
| dc.identifier.volume | 103 | |
| dc.identifier.issue | 12 | |
| dc.identifier.startpage | 763 | |
| dc.identifier.endpage | 764 | |
| dc.contributor.firstauthorID | 727200 | |
