首页> 外文OA文献 >Why is monoalkylation versus bis-alkylation of the Ni(II) complex of the Schiff base of (S)-N-(2-benzoylphenyl)-1-benzylpyrrolidine-2-carboxamide and glycine so selective? MP2 modelling and topological QTAIM analysis of chiral metallocomplex synthons of alpha-amino acids used for the preparation of radiopharmaceuticals for positron emission tomography

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Why is monoalkylation versus bis-alkylation of the Ni(II) complex of the Schiff base of (S)-N-(2-benzoylphenyl)-1-benzylpyrrolidine-2-carboxamide and glycine so selective? MP2 modelling and topological QTAIM analysis of chiral metallocomplex synthons of alpha-amino acids used for the preparation of radiopharmaceuticals for positron emission tomography

机译：为什么（S）-N-（2-苯甲酰基苯基）-1-苄基吡咯烷-2-羧酰胺和甘氨酸的席夫碱Ni（II）配合物的Ni（II）配合物的单烷基化和双烷基化如此选择性？用于制备正电子发射断层扫描放射性药物的α-氨基酸的手性金属络合物合成子的MP2建模和拓扑QTAIM分析

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Popkov, Alexander; Breza, Martin;
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年度 2010
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1. Why is monoalkylation versus bis-alkylation of the Ni(II) complex of the Schiff base of (S)-N-(2-benzoylphenyl)-1-benzylpyrrolidine-2-carboxamide and glycine so selective? MP2 modelling and topological QTAIM analysis of chiral metallocomplex synthons of α-amino acids used for the preparation of radiopharmaceuticals for positron emission tomography [J] . Popkov A., Breza M. Journal of Radioanalytical and Nuclear Chemistry: An International Journal Dealing with All Aspects and Applications of Nuclear Chemistry . 2010,第3期

机译：为什么（S）-N-（2-苯甲酰基苯基）-1-苄基吡咯烷-2-羧酰胺和甘氨酸的席夫碱Ni（II）配合物的Ni（II）配合物的单烷基化和双烷基化如此选择性？用于制备正电子发射断层照相术放射性药物的α-氨基酸手性金属配合物的MP2建模和拓扑QTAIM分析
2. Why is monoalkylation versus bis-alkylation of the Ni(II) complex of the Schiff base of (S)-N-(2-benzoylphenyl)-1-benzylpyrrolidine-2-carboxamide and glycine so selective? MP2 modelling and topological QTAIM analysis of chiral metallocomplex synthons of α-amino acids used for the preparation of radiopharmaceuticals for positron emission tomography [J] . Alexander Popkov, Martin Breza Journal of Radioanalytical and Nuclear Chemistry . 2010,第3期

机译：为什么（S）-N-（2-苯甲酰基苯基）-1-苄基吡咯烷-2-羧酰胺和甘氨酸的席夫碱Ni（II）配合物的Ni（II）配合物的单烷基化和双烷基化如此选择性？用于制备正电子发射断层照相术放射性药物的α-氨基酸手性金属配合物的MP2建模和拓扑QTAIM分析
3. Syntheses, X-ray, MSn, NMR and CD structure determination of nickel(II) complexes of Schiff bases of (S)-N-(2-benzoylphenyl)-1-benzylpyrrolidine-2-carboxamide and aromatic alpha-amino acids [J] . Nadvornik M, Langer V, Jirasko R, Polyhedron: The International Journal for Inorganic and Organometallic Chemistry . 2008,第17期

机译：（S）-N-（2-苯甲酰基苯基）-1-苄基吡咯烷-2-羧酰胺和芳香族α-氨基酸的席夫碱的镍（II）配合物的合成，X射线，MSn，NMR和CD结构测定
4. Why is monoalkylation versus bis-alkylation of the Ni(II) complex of the Schiff base of (S)-N-(2-benzoylphenyl)-1-benzylpyrrolidine-2-carboxamide and glycine so selective? MP2 modelling and topological QTAIM analysis of chiral metallocomplex synthons of α-amino acids used for the preparation of radiopharmaceuticals for positron emission tomography [O] . Alexander Popkov, Martin Breza -1

机译：为什么（S）-N-（2-苯甲酰基苯基）-1-苄基吡咯烷-2-羧酰胺和甘氨酸的席夫碱Ni（II）配合物的Ni（II）配合物的单烷基化和双烷基化如此选择性？用于制备正电子发射断层照相术放射性药物的α-氨基酸手性金属配合物的MP2建模和拓扑QTAIM分析
5. Why is monoalkylation versus bis-alkylation of the Ni(II) complex of the Schiff base of (S)-N-(2-benzoylphenyl)-1-benzylpyrrolidine-2-carboxamide and glycine so selective? MP2 modelling and topological QTAIM analysis of chiral metallocomplex synthons of alpha-amino acids used for the preparation of radiopharmaceuticals for positron emission tomography [O] . Popkov, Alexander, Breza, Martin 2010

机译：为什么（S）-N-（2-苯甲酰基苯基）-1-苄基吡咯烷-2-羧酰胺和甘氨酸的席夫碱Ni（II）配合物的Ni（II）配合物的单烷基化和双烷基化如此选择性？用于制备正电子发射断层扫描放射性药物的α-氨基酸的手性金属络合物合成子的MP2建模和拓扑QTAIM分析

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