Electrochemically Deprotonated Chiral Nickel(II) Glycinate in Stereoselective Nucleophilic Addition to Michael Acceptors: Advantages and Limitations-Reference-Cited by-同舟云学术

Electrochemically Deprotonated Chiral Nickel(II) Glycinate in Stereoselective Nucleophilic Addition to Michael Acceptors: Advantages and Limitations

Published:2014-05-06 Issue:18 Volume:33 Page:4629-4638
ISSN:0276-7333
Container-title:Organometallics
language:en
Short-container-title:Organometallics

Author:

Magdesieva Tatiana V.¹,Levitskiy Oleg A.¹,Grishin Yuri K.¹,Ambartsumyan Asmik A.²,Kiskin Mikhail A.³,Churakov Andrei V.³⁴,Babievsky Konstantin K.²,Kochetkov Konstantin A.²

Affiliation:

1. Department of Chemistry, Lomonosov Moscow State University, Leninskie Gory 1/3, Moscow 119991, Russia

2. Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences, Vavilov str., 28, Moscow, Russia

3. Kurnakov Institute of General and Inorganic Chemistry, Russian Academy of Sciences, Leninsky Prosp. 31, 119991 Moscow, Russia

4. Department of Chemistry, Tomsk State University, Lenina prosp. 36, Tomsk 634050, Russia

Publisher

American Chemical Society (ACS)

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/om500070n

Reference28 articles.

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2. Stereoselective Michael Addition of Glycine Anions to Chiral Fischer Alkenylcarbene Complexes. Asymmetric Synthesis of β-Substituted Glutamic Acids

3. Asymmetric synthesis of α-amino acids via homologation of Ni(II) complexes of glycine Schiff bases; Part 1: alkyl halide alkylations

4. Improved procedures for the synthesis of (S)-2-[N-(N′-benzylprolyl)amino]benzophenone (BPB) and Ni(II) complexes of Schiff's bases derived from BPB and amino acids

5. Oare, D. A.; Heathcock, C. H.InTopics in Stereochemistry;Eliel, E. L.; Wilen, S. H., Eds.Wiley:New York, 1989; Vol.19, pp227–407.

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