Diastereoselective 1,3-dipolar cycloadditions of new azomethine ylides derived from trifluorothioacetamides or cyanothioformamides
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference20 articles.
1. Fluorine in Bioorganic Chemistry;Welch,1991
2. THE TRIFLUOROMETHYL GROUP IN ORGANIC SYNTHESIS. A REVIEW
3. Some influences of fluorine in bioorganic chemistry
4. Pyrrolizidine and Indolizidine Syntheses Involving 1,3-Dipolar Cycloadditions
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2. Synthesis of fluorinated pyrrolizidine, indolizidine and quinolizidine derivatives;Ukr. Bioorg. Acta 2022, Vol. 17, N1;2022-06-30
3. Highly regio- and stereoselective 1,3-dipolar cycloaddition of stabilised azomethine ylides to 3,3,3-trihalogeno-1-nitropropenes: Synthesis of trihalomethylated spiroindenepyrroli(zi)dines;Journal of Fluorine Chemistry;2017-12
4. Squaramide-catalyzed domino Michael/aza-Henry [3 + 2] cycloaddition: asymmetric synthesis of functionalized 5-trifluoromethyl and 3-nitro substituted pyrrolidines;Organic Chemistry Frontiers;2017
5. One-pot synthesis and theoretical calculation for trifluoromethylated pyrrolizidines by 1,3-dipolar cycloaddition with azomethine ylides and β-trifluoromethyl acrylamides;Journal of Fluorine Chemistry;2016-09
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