کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
9591778 | 1507018 | 2005 | 9 صفحه PDF | دانلود رایگان |
عنوان انگلیسی مقاله ISI
The mechanism of enantioselective palladium(0)-catalyzed allylic alkylation with chiral oxazolinylpyridines: a DFT study
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کلمات کلیدی
موضوعات مرتبط
مهندسی و علوم پایه
شیمی
شیمی تئوریک و عملی
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چکیده انگلیسی
The density functional computations of the asymmetric allylic alkylation of (±)tans-1,3-dimethylallyl formate, 2, with malonaldehyde catalyzed by chiral Pd-oxazolinylpyridine are performed. All the structures are optimised completely at the B3LYP/LANL2DZ+P level. As illustrated, this allylic alkylation is endothermic and goes mainly through association of Pd-oxazolinylpyridine with trans-1,3-dimethylallyl formate, oxidative addition of HCOOâ in 2 to Pd, nucleophilic addition of malonaldehyde anion to the Ï-allyl cation complex, and dissociation of the Pd-oxazolinylpyridine-product complex to generate the product with regeneration of the catalyst. The turnover-limiting step for this reaction is the nucleophilic addition of malonaldehyde anion. The main substitution product predicted theoretically is (S)-trans-1,3-dimethylallyl malonaldehyde. The transition states for the oxidative addition and the nucleophilic addition involve a twisted papilionaceous Pd-C-C-C four-membered ring.
ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Journal of Molecular Structure: THEOCHEM - Volume 716, Issues 1â3, 7 March 2005, Pages 79-87
Journal: Journal of Molecular Structure: THEOCHEM - Volume 716, Issues 1â3, 7 March 2005, Pages 79-87
نویسندگان
Dianyong Tang, Xiaoling Luo, Wei Shen, Ming Li,