Show simple item record

dc.contributor.authorŞahin, Engin
dc.date.accessioned2020-11-25T19:02:02Z
dc.date.available2020-11-25T19:02:02Z
dc.date.issued2020en_US
dc.identifier.citationŞahin, E. (2020). Synthesis of enantiopure (S)‐6‐chlorochroman‐4‐ol using whole‐cell Lactobacillus paracasei biotransformation. Chirality, 32(3), 400-406.en_US
dc.identifier.urihttps://onlinelibrary.wiley.com/doi/full/10.1002/chir.23177?casa_token=pSVEoyeBCDIAAAAA%3AZvEhRRpBKTjI_HQITtFImfBEgqFyfG_Gp6lGgulFAgKNOMAIlp-4D8cLJqC3fxLrL8weeBennJ4NTa-R
dc.identifier.urihttps://hdl.handle.net/20.500.12403/2216
dc.description.abstractChromane, which has a fused cyclic structure, is a significant molecule that can be found in the structure of many important compounds. Lactobacillus paracasei BD101 was demonstrated as whole‐cell biocatalyst for the synthesis of (S)‐6‐chlorochroman‐4‐ol with immense enantioselectivity. The conditions of asymmetric reduction were optimized one factor by one factor using L paracasei BD101 to achieve enantiomerically pure product and complete conversion. Using these obtained optimization conditions, asymmetric reduction of 6‐chlorochroman‐4‐one was performed under environmentally friendly conditions; 6‐chlorochroman‐4‐one, having a fused cyclic structure as previously noted to be difficult to asymmetric reduction with biocatalysts, was enantiomerically reduced to (S)‐6‐chlorochroman‐4‐ol with an enantiomeric excess >99% on a high gram scale. This study is the first example in the literature for the enantiopure synthesis of (S)‐6‐chlorochroman‐4‐ol using a biocatalyst. Also notably, the optical purity of (S)‐6‐chlorochroman‐4‐ol obtained in this study through asymmetric bioreduction using whole‐cell biocatalyst is the highest value in the literature. In this study, (S)‐6‐chlorochroman‐4‐ol was produced on a gram scale by an easy, inexpensive, and environmentally friendly method, which has shown the production of valuable chiral precursors for drug synthesis and other industrial applications. This study provides a convenient method for the production of (S)‐6‐chlorochroman‐4‐ol, which can meet the industrial green production demand of this chiral secondary alcohol.en_US
dc.language.isoengen_US
dc.publisherChiralityen_US
dc.relation.isversionof10.1002/chir.23177en_US
dc.subjectChiralityen_US
dc.titleSynthesis of enantiopure (S)‐6‐chlorochroman‐4‐ol using whole‐cell Lactobacillus paracasei biotransformationen_US
dc.typearticleen_US
dc.relation.journalChiralityen_US
dc.contributor.departmentBayburt Üniversitesi, Sağlık Bilimleri Fakültesi, Beslenme ve Diyetetik Bölümüen_US
dc.contributor.authorID0000-0002-3723-1705en_US
dc.identifier.volume32en_US
dc.identifier.issue3en_US
dc.identifier.startpage400en_US
dc.identifier.endpage406en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


Files in this item

FilesSizeFormatView

There are no files associated with this item.

This item appears in the following Collection(s)

Show simple item record