Chemoselective oxidative hydrolysis of EWG protected α-arylamino vinyl bromides to α-arylamino-α′-bromoacetones-Reference-Cited by-同舟云学术

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Chemoselective oxidative hydrolysis of EWG protected α-arylamino vinyl bromides to α-arylamino-α′-bromoacetones

Published:2013-08 Issue:33 Volume:54 Page:4369-4372
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Pace Vittorio,Castoldi Laura,Hernáiz María J.,Alcántara Andrés R.,Holzer Wolfgang

Funder

Austrian Federal Ministry for Science and Research

Spanish Ministry of Science and Innovation and Spanish Ministry of Economic Affairs

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference34 articles.

1. The Chemistry of α-Haloketones α-Haloaldehydes and α-Haloimines;DeKimpe,1988

2. α-Amino-α´-Halomethylketones: Synthetic Methodologies and Pharmaceutical Applications as Serine and Cysteine Protease Inhibitors

3. α-Aminoalkyl-α‘-Halomethylketones: Preparation and Application to Pharmaceutically Interesting Compounds

4. Industrial Syntheses of the Central Core Molecules of HIV Protease Inhibitors

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3. Syntheses of a Pair of Simplified Model Compounds of the Dihydroxycyclopentenone Core of the Kodaistatins A-D;European Journal of Organic Chemistry;2018-11-27

4. Merging lithium carbenoid homologation and enzymatic reduction: A combinative approach to the HIV-protease inhibitor Nelfinavir;Tetrahedron;2018-05

5. A New Approach to Models of the 4,5-Dihydroxycyclopentenone Core of the Kodaistatins A-D: Elucidation of the Diol Configuration in Kodaistatin A;Chemistry - A European Journal;2017-06-27

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