| dc.contributor.author | Onar, Hulya Celik | |
| dc.contributor.author | Hasdemir, Belma | |
| dc.contributor.author | Yusufoglu, Ayşe Sergüzel | |
| dc.date.accessioned | 2021-03-02T23:12:15Z | |
| dc.date.available | 2021-03-02T23:12:15Z | |
| dc.date.issued | 2007 | |
| dc.identifier.citation | Onar H. C. , Hasdemir B., Yusufoglu A. S. , "Asymmetric Meerwein-Ponndorf-Verley reduction of long chain keto alkanoic acid methyl esters", JOURNAL OF THE SERBIAN CHEMICAL SOCIETY, cilt.72, sa.5, ss.421-427, 2007 | |
| dc.identifier.issn | 0352-5139 | |
| dc.identifier.other | av_1109615e-f9bb-4c55-b622-b1f294ea221d | |
| dc.identifier.other | vv_1032021 | |
| dc.identifier.uri | http://hdl.handle.net/20.500.12627/16952 | |
| dc.identifier.uri | https://doi.org/10.2298/jsc0705421o | |
| dc.description.abstract | 3-, 7- and 13-Monoketo tetradecanoic acid methyl esters carrying a keto group at the ends and at the middle of the chain with 14 carbon atoms were reduced by a Meerwein-Ponndorf-Verley reaction in the presence of R-(+)-1,1'-binaphthalcne-2,2'-diol, 1,2:5,6-D-di-O-isopropylidene-D-mannitol and L-(-)-menthol. The highest enantiomeric purity of 65% ee was found for 13-hydroxy ester isomer. The enantiomeric excess was determined by H-1-NMR shift with Eu(tfc)(3) and by optical rotation. | |
| dc.language.iso | eng | |
| dc.subject | Temel Bilimler (SCI) | |
| dc.subject | Alkoloidler | |
| dc.subject | KİMYA, MULTİDİSİPLİNER | |
| dc.subject | Kimya | |
| dc.subject | Biyokimya | |
| dc.subject | Temel Bilimler | |
| dc.title | Asymmetric Meerwein-Ponndorf-Verley reduction of long chain keto alkanoic acid methyl esters | |
| dc.type | Makale | |
| dc.relation.journal | JOURNAL OF THE SERBIAN CHEMICAL SOCIETY | |
| dc.contributor.department | , , | |
| dc.identifier.volume | 72 | |
| dc.identifier.issue | 5 | |
| dc.identifier.startpage | 421 | |
| dc.identifier.endpage | 427 | |
| dc.contributor.firstauthorID | 6478 | |
