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Synthesis of Seven Membered Oxacycles: Recent Developments and New Approaches.
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- European Journal of Organic Chemistry, 2020, v. 2020, n. 43, p. 6704, doi. 10.1002/ejoc.202000850
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Iron(III)-Catalyzed Halogenations by Substitution of Sulfonate Esters.
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- Advanced Synthesis & Catalysis, 2011, v. 353, n. 6, p. 963, doi. 10.1002/adsc.201000740
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- Article
Rotational population dependences of the hydroxymethyl group in alkyl glucopyranosides: Anomers comparison.
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- Chirality, 1997, v. 9, n. 5/6, p. 626, doi. 10.1002/(SICI)1520-636X(1997)9:5/6<626::AID-CHIR34>3.0.CO;2-O
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Factors Controlling the Alkyne Prins Cyclization: The Stability of Dihydropyranyl Cations.
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- Chemistry - A European Journal, 2008, v. 14, n. 20, p. 6260, doi. 10.1002/chem.200800281
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β′-Hydroxy-α,β-unsaturated ketones: A new pharmacophore for the design of anticancer drugs. Part 2.
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- ChemMedChem, 2008, v. 3, n. 11, p. 1740, doi. 10.1002/cmdc.200800212
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Prins-Type Synthesis and SAR Study of Cytotoxic Alkyl Chloro Dihydropyrans.
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- ChemMedChem, 2006, v. 1, n. 3, p. 323, doi. 10.1002/cmdc.200500057
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Enantiodivergent Synthesis of (+)- and (−)-Pyrrolidine 197B: Synthesis of trans-2,5-Disubstituted Pyrrolidines by Intramolecular Hydroamination.
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- Chemistry - A European Journal, 2016, v. 22, n. 43, p. 15529, doi. 10.1002/chem.201602708
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- Article
Prins Cyclization Catalyzed by a Fe<sup>III</sup>/Trimethylsilyl Halide System: The Oxocarbenium Ion Pathway versus the [2+2] Cycloaddition.
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- Chemistry - A European Journal, 2015, v. 21, n. 43, p. 15211, doi. 10.1002/chem.201502488
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Back Cover: Prins Cyclization Catalyzed by a Fe<sup>III</sup>/Trimethylsilyl Halide System: The Oxocarbenium Ion Pathway versus the [2+2] Cycloaddition (Chem. Eur. J. 43/2015).
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- Chemistry - A European Journal, 2015, v. 21, n. 43, p. 15448, doi. 10.1002/chem.201584304
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- Article
Synthesis of Oxazole–Tetrahydropyran Hybrids and Study on Their Antiproliferative Activity Against Human Tumour Cells.
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- European Journal of Organic Chemistry, 2022, v. 2022, n. 39, p. 1, doi. 10.1002/ejoc.202200528
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