中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Analysis of crystallographic structures of Ni(II) complexes of a-amino acid Schiff bases: elucidation of the substituent effect on stereochemical preferences

文献类型:期刊论文

作者Nian, Yong1,5; Wang, Jiang1,5; Moriwaki, Hiroki2; Soloshonok, Vadim A.3,4; Liu, Hong1,5
刊名DALTON TRANSACTIONS
出版日期2017-04-07
卷号46期号:13页码:4191-4198
ISSN号1477-9226
DOI10.1039/c7dt00014f
文献子类Article
英文摘要In this study, we performed critical analysis of 13 crystallographic structures of various Ni(II) complexes of amino acid Schiff bases. The major finding of this work is the significance of a parallel displaced type of aromatic interactions between o-amino-benzophenone and Pro N-benzyl rings. The quality of these aromatic interactions was shown to control the steric environment around the amino acid side-chain, rendering variously substituted Ni(II) complexes of different thermodynamic stabilities. The discovered structural trend holds true for aliphatic, aromatic and sterically bulky amino acids and can be used for the rational design of new and more efficient chiral ligands for general asymmetric synthesis of tailor-made a-amino acids.
WOS关键词EFFICIENT ASYMMETRIC-SYNTHESIS ; NUCLEOPHILIC GLYCINE EQUIVALENTS ; DYNAMIC KINETIC RESOLUTION ; FACE AROMATIC INTERACTIONS ; PI-PI INTERACTIONS ; OPERATIONALLY CONVENIENT CONDITIONS ; PURE 4-AMINOGLUTAMIC ACIDS ; MICHAEL ADDITION-REACTIONS ; NI-II COMPLEXES ; ALPHA-AMINO
资助项目National Natural Science Foundation of China[21632008] ; National Natural Science Foundation of China[81620108207] ; National Natural Science Foundation of China[9122904] ; Major Project of Chinese National Programs for Fundamental Research and Development[2015CB910304] ; National S&T Major Projects[2014ZX09507002-001] ; Ikerbasque[00000000] ; Basque Foundation for Science[00000000]
WOS研究方向Chemistry
语种英语
WOS记录号WOS:000397884100010
出版者ROYAL SOC CHEMISTRY
源URL[http://119.78.100.183/handle/2S10ELR8/272706]  
专题药物化学研究室
通讯作者Soloshonok, Vadim A.; Liu, Hong
作者单位1.Univ Chinese Acad Sci, 19A Yuquan Rd, Beijing 100049, Peoples R China;
2.Hamari Chem Ltd, Higashi Ku, Yodogawa Ku, 1-4-29 Kunijima, Osaka 5330024, Japan;
3.Univ Basque Country UPV EHU, Fac Chem, Dept Organ Chem 1, Paseo Manuel Lardizabal 3, San Sebastian 20018, Spain;
4.Ikerbasque, Basque Fdn Sci, Maria Diaz de Haro 3, Bilbao 48013, Spain
5.Chinese Acad Sci, Shanghai Inst Mat Med, CAS Key Lab Receptor Res, 555 Zuchongzhi Rd, Shanghai 201203, Peoples R China;
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Nian, Yong,Wang, Jiang,Moriwaki, Hiroki,et al. Analysis of crystallographic structures of Ni(II) complexes of a-amino acid Schiff bases: elucidation of the substituent effect on stereochemical preferences[J]. DALTON TRANSACTIONS,2017,46(13):4191-4198.
APA Nian, Yong,Wang, Jiang,Moriwaki, Hiroki,Soloshonok, Vadim A.,&Liu, Hong.(2017).Analysis of crystallographic structures of Ni(II) complexes of a-amino acid Schiff bases: elucidation of the substituent effect on stereochemical preferences.DALTON TRANSACTIONS,46(13),4191-4198.
MLA Nian, Yong,et al."Analysis of crystallographic structures of Ni(II) complexes of a-amino acid Schiff bases: elucidation of the substituent effect on stereochemical preferences".DALTON TRANSACTIONS 46.13(2017):4191-4198.

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来源:上海药物研究所

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