首页> 外文期刊>Tetrahedron, Asymmetry: The International Journal for Repid Publication on all Aspects of Asymmetry in Orgainc, Inorganic, Organometallic, Physical and Bio-Organic Chemistry >Synthesis of novel chiral Ni~(II) complexes of dehydroalanine Schiff bases and their reactivity in asymmetric nucleophilic addition reactions. Novel synthesis of (S)-2-carboxypiperazine
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Synthesis of novel chiral Ni~(II) complexes of dehydroalanine Schiff bases and their reactivity in asymmetric nucleophilic addition reactions. Novel synthesis of (S)-2-carboxypiperazine

机译:脱氢丙氨酸席夫碱新型手性Ni〜(II)配合物的合成及其在不对称亲核加成反应中的反应性(S)-2-羧基哌嗪的新型合成

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摘要

New chiral Ni~(II) complexes of Schiff bases of dehydroalanine with modified chiral auxiliaries (S)-2-N-[N′-(3,4-dichlorobenzyl)prolyl] aminobenzophenone (3,4-DCBPB), (S)-2-N-[N′-(3,4-dimethylbenzyl)prolyl] aminobenzophenone (3,4-DMBPB), (S)-2-N-[N′-(2-chlorobenzyl)prolyl] aminobenzophenone (2-CBPB), and (S)-2-N-[N′-(2-fluorobenzyl)prolyl]- aminobenzophenone (2-FBPB) have been synthesized. Asymmetric Michael addition reactions of primary and secondary amines and thiols to the dehydroalanine moieties of the complexes were studied. (S)-2-FBPB was found to be the best chiral auxiliary in terms of both selectivity of the reactions (de ~92-96%) and reactivity of the complexes. A novel synthetic route toward (S)-2-carboxypiperazine was developed based on the auxiliary.
机译:脱氢丙氨酸席夫碱与改性手性助剂(S)-2-N- [N'-(3,4-二氯苄基)脯氨酰基]氨基二苯甲酮(3,4-DCBPB),(S)的新手性Ni〜(II)配合物-2-N- [N'-(3,4-二甲基苄基)脯氨酰基]氨基二苯甲酮(3,4-DMBPB),(S)-2-N- [N'-(2-氯苄基)脯氨酰基]氨基二苯甲酮(2- CBPB)和(S)-2-N- [N'-(2-氟苄基)脯氨酰基]-氨基二苯甲酮(2-FBPB)已经合成。研究了伯胺和仲胺与硫醇对配合物的脱氢丙氨酸部分的不对称迈克尔加成反应。从反应的选择性(de〜92-96%)和配合物的反应性两方面来看,(S)-2-FBPB是最佳的手性助剂。基于该助剂,开发了一种新的合成(S)-2-羧基哌嗪的合成途径。

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