دورية أكاديمية

Fungi mediated conversion of benzil to benzoin and hydrobenzoin

التفاصيل البيبلوغرافية
العنوان: Fungi mediated conversion of benzil to benzoin and hydrobenzoin
المؤلفون: Demir, AS, Hamamcı, Haluk, Ayhan, P, Duygu, AN, Igdir, AC, Capanoglu, D
بيانات النشر: TETRAHEDRON-ASYMMETRY
سنة النشر: 2004
مصطلحات موضوعية: Ligand, Cleavage, Auxiliary, Convenient, Reduction, Aryl aldehydes, Hydroxy ketones, Kinetic resolution, Enantioselective synthesis, Asymmetric dihydroxylation
الوصف: An enzyme system of four fungi catalyses the reduction of benzil to benzoin, as well as benzoin to hydrobenzoin. Depending on the pH of the medium, both enantiomers of benzoin can be obtained in good yield and high ee starting from benzil via a reduction, as well as from rac-benzoin via a novel deracemization reaction. Starting from benzil, (R)-, (S)- and rac-benzoin only (R,R)-hydrobenzoin was obtained in high ee and chemical yield.
نوع الوثيقة: article in journal/newspaper
اللغة: unknown
تدمد: 0957-4166
العلاقة: Demir A., Hamamci H., Ayhan P., Duygu A., Igdir A., Capanoglu D., "Fungi mediated conversion of benzil to benzoin and hydrobenzoin", TETRAHEDRON-ASYMMETRY, cilt.15, ss.2579-2582, 2004; 2582; 16; 2579; https://hdl.handle.net/11511/30834Test; 15; WOS:000223666600019
DOI: 10.1016/j.tetasy.2004.07.010
الإتاحة: https://doi.org/10.1016/j.tetasy.2004.07.010Test
https://hdl.handle.net/11511/30834Test
حقوق: Attribution-NonCommercial-NoDerivatives 4.0 International ; http://creativecommons.org/licenses/by-nc-nd/4.0Test/
رقم الانضمام: edsbas.B0EEC57D
قاعدة البيانات: BASE
الوصف
تدمد:09574166
DOI:10.1016/j.tetasy.2004.07.010