Addition of alkyl radicals, generated from carboxylic acids via photochemical decarboxylation, to glyoxylic oxime ether: a mild and efficient route to α-substituted α-aminoesters-Reference-Cited by-同舟云学术

Addition of alkyl radicals, generated from carboxylic acids via photochemical decarboxylation, to glyoxylic oxime ether: a mild and efficient route to α-substituted α-aminoesters

Published:2010-04 Issue:17 Volume:51 Page:2332-2334
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Yoshimi Yasuharu,Kobayashi Kosuke,Kamakura Hayato,Nishikawa Keisuke,Haga Yoshiki,Maeda Kousuke,Morita Toshio,Itou Tatsuya,Okada Yutaka,Hatanaka Minoru

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference19 articles.

1. Intermolecular alkyl radical addition to the carbon-nitrogen double bond of oxime ethers and hydrazones

2. Asymmetric Synthesis of α-Amino Acids Based on Carbon Radical Addition to Glyoxylic Oxime Ether

3. Free-Radical Reaction of Imine Derivatives in Water

4. Asymmetric synthesis of α-amino acids: indium-mediated reactions of glyoxylic oxime ether in aqueous mediaElectronic supplementary information (ESI) available: typical procedures for allylation reaction and isopropyl radical addition reaction. See http://www.rsc.org/suppdata/cc/b2/b203493j/

5. Carbon–carbon bond construction on solid support: triethylborane-induced radical reactions of oxime ethers

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5. Decatungstate‐Photocatalyzed Functionalization of α‐Imino Esters for the Preparation of Unnatural α‐Amino Acid Derivatives;ChemCatChem;2023-04-12