| dc.contributor.author | Hasdemir, Belma | |
| dc.contributor.author | Yusufoglu, Ayşe Sergüzel | |
| dc.date.accessioned | 2021-03-02T20:52:38Z | |
| dc.date.available | 2021-03-02T20:52:38Z | |
| dc.date.issued | 2004 | |
| dc.identifier.citation | Hasdemir B., Yusufoglu A. S. , "Asymmetric synthesis of monohydroxy tetradecanoic acids and their methyl esters", TETRAHEDRON-ASYMMETRY, cilt.15, sa.1, ss.65-68, 2004 | |
| dc.identifier.issn | 0957-4166 | |
| dc.identifier.other | av_041e2055-3a42-41e2-bc29-5849a22c84c0 | |
| dc.identifier.other | vv_1032021 | |
| dc.identifier.uri | http://hdl.handle.net/20.500.12627/8704 | |
| dc.identifier.uri | https://doi.org/10.1016/j.tetasy.2003.10.020 | |
| dc.description.abstract | Methyl 3-, 6- and 13-oxo tetradecanoates were reduced by NaBH4 in the presence of 1,2:5,6-di-O-isopropylidene-Dglucofuranose (DIPGH) and (-)-menthol together with isovaleric and pivalic acids in THF solution. The highest enantiomeric purity was found for the 13-hydroxy ester isomer of 96%, ee. Enantiomeric excess (ee, %) was determined by chiral HPLC and H-1 NNIR with shift reagent, EU(tfc)(3). (C) 2003 Elsevier Ltd. All rights reserved. | |
| dc.language.iso | eng | |
| dc.subject | KİMYA, FİZİKSEL | |
| dc.subject | İnorganik Kimya | |
| dc.subject | Temel Bilimler | |
| dc.subject | Biyoinorganik Kimya | |
| dc.subject | Biyokimya | |
| dc.subject | Fizikokimya | |
| dc.subject | KİMYA, İNORGANİK VE NÜKLEER | |
| dc.subject | Kimya | |
| dc.subject | Temel Bilimler (SCI) | |
| dc.subject | KİMYA, ORGANİK | |
| dc.title | Asymmetric synthesis of monohydroxy tetradecanoic acids and their methyl esters | |
| dc.type | Makale | |
| dc.relation.journal | TETRAHEDRON-ASYMMETRY | |
| dc.contributor.department | İstanbul Üniversitesi , Mühendislik Fakültesi , Kimya | |
| dc.identifier.volume | 15 | |
| dc.identifier.issue | 1 | |
| dc.identifier.startpage | 65 | |
| dc.identifier.endpage | 68 | |
| dc.contributor.firstauthorID | 6495 | |
