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Highly Efficient Asymmetric Morita–Baylis–Hillman Reaction Promoted by Chiral Aziridine-Phosphines.
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- Catalysts (2073-4344), 2022, v. 12, n. 4, p. 394, doi. 10.3390/catal12040394
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Efficient Asymmetric Simmons-Smith Cyclopropanation and Diethylzinc Addition to Aldehydes Promoted by Enantiomeric Aziridine-Phosphines.
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- Catalysts (2073-4344), 2021, v. 11, n. 8, p. 968, doi. 10.3390/catal11080968
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Asymmetric Friedel–Crafts Alkylation of Indoles Catalyzed by Chiral Aziridine-Phosphines.
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- Catalysts (2073-4344), 2020, v. 10, n. 9, p. 971, doi. 10.3390/catal10090971
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Enantioselective Mannich Reaction Promoted by Chiral Phosphinoyl-Aziridines.
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- Catalysts (2073-4344), 2019, v. 9, n. 10, p. 837, doi. 10.3390/catal9100837
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- Article
Chiral Aziridine Phosphines as Highly Effective Promoters of Asymmetric Rauhut–Currier Reaction.
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- Symmetry (20738994), 2022, v. 14, n. 8, p. 1631, doi. 10.3390/sym14081631
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Recent Advances in Selected Asymmetric Reactions Promoted by Chiral Catalysts: Cyclopropanations, Friedel–Crafts, Mannich, Michael and Other Zinc-Mediated Processes—An Update.
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- Symmetry (20738994), 2021, v. 13, n. 10, p. 1762, doi. 10.3390/sym13101762
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- Article
Enantiodivergent Aldol Condensation in the Presence of Aziridine/Acid/Water Systems.
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- Symmetry (20738994), 2020, v. 12, n. 6, p. 930, doi. 10.3390/sym12060930
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- Article
Flash Vacuum Thermolysis of N-(3- and 4-Pyridylmethylidene)- tert-butylamines: Mechanisms of Formation of Pyrrolopyridines and Naphthyridines.
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- European Journal of Organic Chemistry, 2014, v. 2014, n. 14, p. 3020, doi. 10.1002/ejoc.201400112
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Flash Vacuum Thermolysis of 1-Azabicyclo[1.1.0]butanes. Photoelectron Spectrum of 3-Phenyl-2-azabuta-1,3-diene.
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- European Journal of Organic Chemistry, 2003, v. 2003, n. 13, p. 2475, doi. 10.1002/ejoc.200300060
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- Article
New Reactions of N-tert-Butylimines; Formation of N-Heterocycles by Methyl Radical Elimination on Flash Vacuum Thermolysis of N-Benzylidene- and N-(2-Pyridylmethylidene)- tert-butylamines.
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- Chemistry - A European Journal, 2013, v. 19, n. 44, p. 14983, doi. 10.1002/chem.201301663
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- Article
Aziridine Ring Opening as Regio- and Stereoselective Access to C -Glycosyl-Aminoethyl Sulfide Derivatives.
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- Molecules, 2022, v. 27, n. 6, p. 1764, doi. 10.3390/molecules27061764
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Synthesis and Evaluation of Biological Activities of Aziridine Derivatives of Urea and Thiourea.
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- Molecules, 2018, v. 23, n. 1, p. 45, doi. 10.3390/molecules23010045
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- Article
Highly enantioselective asymmetric direct aldol reaction promoted by aziridine amides constructed on chiral terpene scaffold.
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- Chirality, 2017, v. 29, n. 5, p. 213, doi. 10.1002/chir.22698
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Studies on the Flash Vacuum Thermolysis of Thiones of Selected N-, O-, and S-Heterocycles.
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- Helvetica Chimica Acta, 2006, v. 89, n. 5, p. 991
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- Article
Highly Efficient Asymmetric Aziridination of Unsaturated Aldehydes Promoted by Chiral Hetero-organic Catalysts.
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- ChemCatChem, 2015, v. 7, n. 21, p. 3589, doi. 10.1002/cctc.201500537
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- Article
Highly Efficient Asymmetric Simmons-Smith Cyclopropanation Promoted by Chiral Heteroorganic Aziridinyl Ligands.
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- ChemCatChem, 2014, v. 6, n. 3, p. 873, doi. 10.1002/cctc.201300883
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Recent progress in the synthesis of aziridine derivatives (microreview).
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- Chemistry of Heterocyclic Compounds, 2016, v. 52, n. 6, p. 353, doi. 10.1007/s10593-016-1893-8
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Synthesis of chiral 1-(2-aminoalkyl)aziridines via a self-opening reaction of aziridine.
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- ARKIVOC: Online Journal of Organic Chemistry, 2017, v. 2017, p. 223, doi. 10.3998/ark.5550190.p009.741
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- Article