Stereoselective electrochemical thioalkylation of glycine in Ni(II) coordination environment-Reference-Cited by-同舟云学术

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Stereoselective electrochemical thioalkylation of glycine in Ni(II) coordination environment

Published:2018-07 Issue:29 Volume:59 Page:2831-2834
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Levitskiy Oleg A.,Grishin Yuri K.,Paseshnichenko Ksenia A.,Kochetkov Konstantin A.,Magdesieva Tatiana V.

Funder

Russian Foundation for Basic Research

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference20 articles.

1. Organic Electrochemistry, 5th ed.,2016

2. Catalytic Methods In Asymmetric Synthesis Advanced Materials, Techniques, and Applications,2011

3. General method of diastereo- and enantioselective synthesis of β-hydroxy-α-amino acids by condensation of aldehydes and ketones with glycine

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

5. Asymmetric synthesis of α-amino acids via homologation of Ni(II) complexes of glycine Schiff bases. Part 2: Aldol, Mannich addition reactions, deracemization and (S) to (R) interconversion of α-amino acids

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1. Advances in Asymmetric Electrochemical Synthesis;Chinese Journal of Organic Chemistry;2024

2. Reductive opening of a cyclopropane ring in the Ni(II) coordination environment: a route to functionalized dehydroalanine and cysteine derivatives;Beilstein Journal of Organic Chemistry;2022-09-08

3. Corey‐Сhaykovsky cyclopropanation of dehydroalanine in the Ni(II) coordination environment: Electrochemical vs. chemical activation;Electrochimica Acta;2022-03

4. Recent advances in transition metal-catalyzed asymmetric electrocatalysis;Coordination Chemistry Reviews;2021-10

5. Diastereomeric Ni(II) Schiff-base cysteine derivatives: Non-covalent interactions and redox activity;Electrochimica Acta;2021-08

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