کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
1326931 | 977452 | 2008 | 6 صفحه PDF | دانلود رایگان |
عنوان انگلیسی مقاله ISI
Further ‘tethered’ Ru(II) catalysts for asymmetric transfer hydrogenation (ATH) of ketones; the use of a benzylic linker and a cyclohexyldiamine ligand
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کلمات کلیدی
موضوعات مرتبط
مهندسی و علوم پایه
شیمی
شیمی معدنی
پیش نمایش صفحه اول مقاله

چکیده انگلیسی
The synthesis and characterisation of two new Ru(II) catalysts for the asymmetric transfer hydrogenation (ATH) of ketones is described. In the case of 4, the novelty lies in the use of a benzyl tethering group between the asymmetric ligand part (TsDPEN) and the η6-arene ring, which increases the complex rigidity. For 5, the use of a cyclohexyldiamine as a chiral ligand is described for the first time. In the ATH of ketones in formic acid/triethylamine, alcohols with ees of up to 97% were formed.
The synthesis, characterisation and application to the asymmetric transfer hydrogenation (ATH) of ketones, of two new Ru(II) catalysts, 4 and 5, is described.Figure optionsDownload as PowerPoint slide
ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Journal of Organometallic Chemistry - Volume 693, Issue 23, 1 November 2008, Pages 3527–3532
Journal: Journal of Organometallic Chemistry - Volume 693, Issue 23, 1 November 2008, Pages 3527–3532
نویسندگان
Jose E.D. Martins, David J. Morris, Bhavana Tripathi, Martin Wills,