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Enantiomeric composition of natural pericosine A derived from Periconia byssoides and α‐glycosidase inhibitory activity of (−)‐enantiomer.
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- Chirality, 2022, v. 34, n. 10, p. 1320, doi. 10.1002/chir.23491
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- Article
Natural pericosines B and C as enantiomeric mixtures: Direct evidence by chiral HPLC analysis.
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- Chirality, 2011, v. 23, n. 1E, p. E7, doi. 10.1002/chir.20937
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- Article
Three New Lanostane Triterpenoids from Inonotus obliquus.
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- Helvetica Chimica Acta, 2007, v. 90, n. 11, p. 2047, doi. 10.1002/hlca.200790214
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- Article
Synthesis of 6-Halo-Substituted Pericosine A and an Evaluation of Their Antitumor and Antiglycosidase Activities.
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- Marine Drugs, 2022, v. 20, n. 7, p. 438, doi. 10.3390/md20070438
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- Article
Syntheses and Glycosidase Inhibitory Activities, and in Silico Docking Studies of Pericosine E Analogs Methoxy-Substituted at C6.
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- Marine Drugs, 2020, v. 18, n. 4, p. 221, doi. 10.3390/md18040221
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- Article
Synthesis of Natural O-Linked Carba-Disaccharides, (+)- and (--)-Pericosine E, and Their Analogues as α-Glucosidase Inhibitors.
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- Marine Drugs, 2017, v. 15, n. 1, p. 22, doi. 10.3390/md15010022
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- Article
5-Hydroxymethyl-2-furfural, a clinical trials agent for sickle cell anemia, and its mono/di-glucosides from classically processed steamed Rehmanniae Radix.
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- Journal of Natural Medicines, 2008, v. 62, n. 2, p. 164, doi. 10.1007/s11418-007-0206-z
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- Article
CuI-Catalyzed Coupling Reactions of 4-Iodopyrazoles and Alcohols: Application toward Withasomnine and Homologs.
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- Molecules, 2021, v. 26, n. 11, p. 3370, doi. 10.3390/molecules26113370
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- Article
C4-Alkylamination of C4-Halo-1 H -1-tritylpyrazoles Using Pd(dba) 2 or CuI.
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- Molecules, 2020, v. 25, n. 20, p. 4634, doi. 10.3390/molecules25204634
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- Article
Synthesis of Dihydropyrano[3,2-c]pyrazoles via Double Bond Migration and Ring-Closing Metathesis.
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- Molecules, 2019, v. 24, n. 2, p. 296, doi. 10.3390/molecules24020296
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- Article
Synthesis of Dihydrooxepino[3,2-c]Pyrazoles via Claisen Rearrangement and Ring-Closing Metathesis from 4-Allyloxy-1H-pyrazoles.
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- Molecules, 2018, v. 23, n. 3, p. 592, doi. 10.3390/molecules23030592
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- Article