A versatile radical based approach to O-alkylated hydroxylamines and oximes
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference23 articles.
1. 17β-O-Aminoalkyloximes of 5β-Androstane-3β,14β-diol with Digitalis-like Activity: Synthesis, Cardiotonic Activity, Structure−Activity Relationships, and Molecular Modeling of the Na+,K+-ATPase Receptor
2. Introduction of aliphatic amino and hydroxy groups to keto steroids using O-substituted hydroxylamines
3. Head-to-Tail Oxime Cyclization of Oligodeoxynucleotides for the Efficient Synthesis of Circular DNA Analogues
4. Efficient Conjugation and Characterization of Distamycin-Based Peptides with Selected Oligonucleotide Stretches
5. Facile synthesis of homogeneous artificial proteins
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1. The Xanthate Route to Ketones: When the Radical Is Better than the Enolate;Accounts of Chemical Research;2018-06-22
2. The xanthate route to organofluorine derivatives. A brief account;Organic & Biomolecular Chemistry;2016
3. Direct cycle between co-product and reactant: an approach to improve the atom economy and its application in the synthesis and protection of primary amines;Green Chemistry;2016
4. Radical-Based Route to 2-(Trifluoromethyl)-1,3,4-oxadiazoles and Trifluoromethyl-Substituted Polycyclic 1,2,4-Triazoles and Dihydrofurans;Organic Letters;2015-03-03
5. Some aspects of radical chemistry in the assembly of complex molecular architectures;Beilstein Journal of Organic Chemistry;2013-03-18
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