Dialkylzinc mediated radical additions to chiral N-enoyloxazolidinones in the presence of benzaldehyde. Mechanistic investigation, structural characterization of the resulting γ-lactones-Reference-Cited by-同舟云学术

Dialkylzinc mediated radical additions to chiral N-enoyloxazolidinones in the presence of benzaldehyde. Mechanistic investigation, structural characterization of the resulting γ-lactones

Published:2005-04 Issue:17 Volume:61 Page:4261-4274
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Bazin Samantha,Feray Laurence,Vanthuyne Nicolas,Bertrand Michèle P.

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference32 articles.

1. Initiation of tin-mediated radical reactions by diethylzinc-air

2. Diethylzinc Mediated Radical Additions to Glyoxylate Imines

3. Et3B- and Et2Zn-Mediated Radical Additions to Glyoxylate Imines, Compared Stereoinductions

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

5. Stereocontrol in Solid-Phase Radical Reactions: Radical Addition to Oxime Ether Anchored to Polymer Support

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1. α-(Aminomethyl)acrylates as acceptors in radical–polar crossover 1,4-additions of dialkylzincs: insights into enolate formation and trapping;Beilstein Journal of Organic Chemistry;2023-09-21

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3. 2.5 Radical–Polar Crossover Reactions;Free Radicals: Fundamentals and Applications in Organic Synthesis 2;2021

4. Multicomponent Radical Processes: Recent Developments;Multi‐component Reactions in Molecular Diversity;2019-12-18

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