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Claudio D Navo

Showing results (1-10 of 45) with videos related to

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ACS Medicinal Chemistry Letters|November 19, 2021
Computer Prediction of p<i>K</i> <sub>a</sub> Values in Small Molecules and ProteinsClaudio D Navo, Gonzalo Jiménez-Osés
Chembiochem : a European Journal of Chemical Biology|January 17, 2019
Elusive Dehydroalanine Derivatives with Enhanced ReactivityCarlos Aydillo, Nuria Mazo, Claudio D Navo, et al.
Journal of the American Chemical Society|May 10, 2024
Darobactin Substrate Engineering and Computation Show Radical Stability Governs Ether versus C-C Bond FormationAustin M Woodard, Francesca Peccati, Claudio D Navo, et al.
Biorxiv : the Preprint Server for Biology|December 11, 2023
Benzylic Radical Stabilization Permits Ether Formation During Darobactin BiosynthesisAustin M Woodard, Francesca Peccati, Claudio D Navo, et al.
Organic & Biomolecular Chemistry|July 4, 2020
Selective modification of sulfamidate-containing peptidesNuria Mazo, Claudio D Navo, Jesús M Peregrina, et al.
Organic Letters|September 9, 2022
Stereoselective α-Deuteration of Serine, Cysteine, Selenocysteine, and 2,3-Diaminopropanoic Acid DerivativesClaudio D Navo, Paula Oroz, Nuria Mazo, et al.
Angewandte Chemie (International Ed. in English)|January 5, 2023
Iridium-Catalyzed ortho-Selective Borylation of Aromatic Amides Enabled by 5-Trifluoromethylated Bipyridine LigandsDaniel Marcos-Atanes, Cristian Vidal, Claudio D Navo, et al.
Organic & Biomolecular Chemistry|October 6, 2021
Nucleophilic catalysis of p-substituted aniline derivatives in acylhydrazone formation and exchangeAndrea Canal-Martín, Claudio D Navo, Elena Sáez, et al.
The Journal of Organic Chemistry|November 18, 2017
Substituent Effects on the Reactivity of Cyclic Tertiary SulfamidatesClaudio D Navo, Nuria Mazo, Alberto Avenoza, et al.
Chembiochem : a European Journal of Chemical Biology|February 19, 2019
Tetrazine-Triggered Release of Carboxylic-Acid-Containing Molecules for Activation of an Anti-inflammatory DrugSarah Davies, Luxi Qiao, Bruno L Oliveira, et al.
Pageof 5

Showing results (1-10 of 45) with videos related to

Sort By:
Pageof 5
ACS Medicinal Chemistry Letters|November 19, 2021
Computer Prediction of p<i>K</i> <sub>a</sub> Values in Small Molecules and ProteinsClaudio D Navo, Gonzalo Jiménez-Osés
Chembiochem : a European Journal of Chemical Biology|January 17, 2019
Elusive Dehydroalanine Derivatives with Enhanced ReactivityCarlos Aydillo, Nuria Mazo, Claudio D Navo, et al.
Journal of the American Chemical Society|May 10, 2024
Darobactin Substrate Engineering and Computation Show Radical Stability Governs Ether versus C-C Bond FormationAustin M Woodard, Francesca Peccati, Claudio D Navo, et al.
Biorxiv : the Preprint Server for Biology|December 11, 2023
Benzylic Radical Stabilization Permits Ether Formation During Darobactin BiosynthesisAustin M Woodard, Francesca Peccati, Claudio D Navo, et al.
Organic & Biomolecular Chemistry|July 4, 2020
Selective modification of sulfamidate-containing peptidesNuria Mazo, Claudio D Navo, Jesús M Peregrina, et al.
Organic Letters|September 9, 2022
Stereoselective α-Deuteration of Serine, Cysteine, Selenocysteine, and 2,3-Diaminopropanoic Acid DerivativesClaudio D Navo, Paula Oroz, Nuria Mazo, et al.
Angewandte Chemie (International Ed. in English)|January 5, 2023
Iridium-Catalyzed ortho-Selective Borylation of Aromatic Amides Enabled by 5-Trifluoromethylated Bipyridine LigandsDaniel Marcos-Atanes, Cristian Vidal, Claudio D Navo, et al.
Organic & Biomolecular Chemistry|October 6, 2021
Nucleophilic catalysis of p-substituted aniline derivatives in acylhydrazone formation and exchangeAndrea Canal-Martín, Claudio D Navo, Elena Sáez, et al.
The Journal of Organic Chemistry|November 18, 2017
Substituent Effects on the Reactivity of Cyclic Tertiary SulfamidatesClaudio D Navo, Nuria Mazo, Alberto Avenoza, et al.
Chembiochem : a European Journal of Chemical Biology|February 19, 2019
Tetrazine-Triggered Release of Carboxylic-Acid-Containing Molecules for Activation of an Anti-inflammatory DrugSarah Davies, Luxi Qiao, Bruno L Oliveira, et al.
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