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Identification of microbes isolated with test kits through culture-dependent and metabarcoding techniques for assessment of microbial corrosion - ScienceDirect
Lewis acid-catalyzed reactions of donor–acceptor cyclopropanes with furan derivatives - ScienceDirect
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Synthesis of Spirocyclic Indolenines - James - 2016 - Chemistry – A European Journal - Wiley Online Library
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JoF | Free Full-Text | Chaetomugilins and Chaetoviridins—Promising Natural Metabolites: Structures, Separation, Characterization, Biosynthesis, Bioactivities, Molecular Docking, and Molecular Dynamics
Brønsted Acid-Controlled [3 + 2] Coupling Reaction of Quinone Monoacetals with Alkene Nucleophiles: A Catalytic System of Perfluorinated Acids and Hydrogen Bond Donor for the Construction of Benzofurans | The Journal of Organic Chemistry
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Perfluoroaryl and Perfluoroheteroaryl Reagents as Emerging New Tools for Peptide Synthesis, Modification and Bioconjugation - Brittain - 2022 - Chemistry – A European Journal - Wiley Online Library
In Situ Formation of N-Trifluoroacetoxy Succinimide (TFA-NHS): One-Pot Formation of Succinimidyl Esters, N-Trifluoroacetyl Amino Acid Succinimidyl Esters, and N-Maleoyl Amino Acid Succinimidyl Esters | The Journal of Organic Chemistry
Catalysts | Free Full-Text | Direct Catalytic Amidations from Carboxylic Acid and Ester Derivatives: A Review
Brønsted Acid-Controlled [3 + 2] Coupling Reaction of Quinone Monoacetals with Alkene Nucleophiles: A Catalytic System of Perfluorinated Acids and Hydrogen Bond Donor for the Construction of Benzofurans | The Journal of Organic Chemistry
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Brønsted Acid-Controlled [3 + 2] Coupling Reaction of Quinone Monoacetals with Alkene Nucleophiles: A Catalytic System of Perfluorinated Acids and Hydrogen Bond Donor for the Construction of Benzofurans | The Journal of Organic Chemistry
Stepwise recombination suppression around the mating-type locus in an ascomycete fungus with self-fertile spores | PLOS Genetics
In Situ Formation of N-Trifluoroacetoxy Succinimide (TFA-NHS): One-Pot Formation of Succinimidyl Esters, N-Trifluoroacetyl Amino Acid Succinimidyl Esters, and N-Maleoyl Amino Acid Succinimidyl Esters | The Journal of Organic Chemistry
In Situ Formation of N-Trifluoroacetoxy Succinimide (TFA-NHS): One-Pot Formation of Succinimidyl Esters, N-Trifluoroacetyl Amino Acid Succinimidyl Esters, and N-Maleoyl Amino Acid Succinimidyl Esters | The Journal of Organic Chemistry
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