Trifluoromethyl-substituted Δ3-imidazolines: Synthesis and reactivity
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference6 articles.
1. Trifluoromethyl-Substituted Imidazolines: Novel Precursors of Trifluoromethyl Ketones Amenable to Peptide Synthesis
2. NEW 1,3-DIPOLAR CYCLOADDITION LEADING TO 2,5-DIHYDROPYRROLE AND PYRROLIDINE DERIVATIVES
3. 1,3-Dipolar cycloaddition leading to N-acylated pyrrolidines and 2,5-dihydropyrroles.
4. [(9-Fluorenylmethyl)oxy]carbonyl (FMOC) amino acid fluorides. Convienient new peptide coupling reagents applicable to the FMOC/tert-butyl strategy for solution and solid-phase syntheses.
5. tert-Butyloxycarbonyl and benzyloxycarbonyl amino acid fluorides. New, stable rapid-acting acylating agents for peptide synthesis
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1. Electrochemical tandem trifluoromethylation of allylamines/formal (3 + 2)-cycloaddition for the rapid access to CF3-containing imidazolines and oxazolidines;Organic Chemistry Frontiers;2021
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3. Regio- and Stereoselective 1,3-Dipolar Cycloaddition of Cyclic Azomethine Imines to Platinum(IV)-Bound Nitriles Giving Δ2-1,2,4-Triazoline Species;Inorganic Chemistry;2015-11-04
4. ChemInform Abstract: Trifluoromethyl-Substituted δ3-Imidazolines: Synthesis and Reactivity.;ChemInform;2010-08-03
5. Comparative Theoretical Study of 1,3-Dipolar Cycloadditions of Allyl-Anion Type Dipoles to Free and Pt-Bound Nitriles;The Journal of Organic Chemistry;2010-02-08
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