One-pot synthesis and theoretical calculation for trifluoromethylated pyrrolizidines by 1,3-dipolar cycloaddition with azomethine ylides and β-trifluoromethyl acrylamides
Author:
Publisher
Elsevier BV
Subject
Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Environmental Chemistry,Biochemistry
Reference62 articles.
1. Naturally Occurring Pyrrolizidine Alkaloids;Rizk,1999
2. Recent advances in the synthesis of naturally occurring pyrrolidines, pyrrolizidines and indolizidine alkaloids using proline as a unique chiral synthon
3. For recent reviews for pyrrolizidine syntheses, see the following:
4. Pyrrolizidine Alkaloids Pyrrolams A-D: A Survey of Synthetic Efforts, Biological Activity, and Studies on Their Stability
5. Asymmetric Synthesis of Polyfunctionalized Pyrrolidines and Related Alkaloids
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1. Decarboxylative 1,3-dipolar cycloadditions of l-proline;RSC Advances;2024
2. Cu(i)-catalysed cross-coupling reaction of in situ generated azomethine ylides towards easy construction of fused N-heterocycles;Chemical Communications;2023
3. Ring expansion and fused cyclization catalysis to construct indoloquinazolinones with functionalization;Chemical Communications;2023
4. Synthesis of 2-trifluoromethylated 3-pyrrolines/pyrrolidines via [3+2] cycloaddition of azomethine ylides with the participation of 3,3,3-trifluoroalanine;Journal of Fluorine Chemistry;2022-12
5. Synthesis of fluorinated pyrrolizidine, indolizidine and quinolizidine derivatives;Ukr. Bioorg. Acta 2022, Vol. 17, N1;2022-06-30
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