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Fernando Albericio

Showing results (151-160 of 524) with videos related to

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Chemistry (Weinheim an Der Bergstrasse, Germany)|March 22, 2016
Synthesis of (E)-4-Bromo-3-methoxybut-3-en-2-one, the Key Fragment in the Polyhydroxylated Chain Common to Oscillariolide and Phormidolides A-CAlejandro Gil, Janire Lamariano-Merketegi, Adriana Lorente, et al.
The Journal of Organic Chemistry|January 24, 1997
Total Synthesis of Dehydrodidemnin B. Use of Uronium and Phosphonium Salt Coupling Reagents in Peptide Synthesis in SolutionGemma Jou, Isabel González, Fernando Albericio, et al.
Molecular Pharmaceutics|August 19, 2010
The antitumoral depsipeptide IB-01212 kills Leishmania through an apoptosis-like process involving intracellular targetsJuan R Luque-Ortega, Luis J Cruz, Fernando Albericio, et al.
The Journal of Organic Chemistry|November 25, 2010
Isolation, structural assignment, and total synthesis of barmumycinAdriana Lorente, Daniel Pla, Librada M Cañedo, et al.
Journal of Peptide Science : an Official Publication of the European Peptide Society|November 19, 2013
Inhibitory effect of short cationic homopeptides against gram-positive bacteriaFanny Guzmán, Sergio Marshall, Claudia Ojeda, et al.
Journal of Peptide Science : an Official Publication of the European Peptide Society|May 29, 2013
COMU: scope and limitations of the latest innovation in peptide acyl transfer reagentsRamon Subirós-Funosas, Lidia Nieto-Rodriguez, Knud J Jensen, et al.
Chemmedchem|April 3, 2008
Use of N-methylpiperazine for the preparation of piperazine-based unsymmetrical bis-ureas as anti-HIV agentsAyman El-Faham, Mercedes Armand-Ugón, Jose A Esté, et al.
Organic Letters|March 15, 2019
Pseudo-Wang Handle for the Preparation of Fully Protected Peptides. Synthesis of Liraglutide by Fragment CondensationDaniel Carbajo, Peter Fransen, Ayman El-Faham, et al.
Chemistry (Weinheim an Der Bergstrasse, Germany)|July 4, 2009
Oxyma: an efficient additive for peptide synthesis to replace the benzotriazole-based HOBt and HOAt with a lower risk of explosionRamon Subirós-Funosas, Rafel Prohens, Rafael Barbas, et al.
The Journal of Organic Chemistry|August 30, 2008
THAL, a sterically unhindered linker for the solid-phase synthesis of acid-sensitive protected peptide acidsAlbert Isidro-Llobet, Ulrik Boas, Knud J Jensen, et al.
Pageof 53

Showing results (151-160 of 524) with videos related to

Sort By:
Pageof 53
Chemistry (Weinheim an Der Bergstrasse, Germany)|March 22, 2016
Synthesis of (E)-4-Bromo-3-methoxybut-3-en-2-one, the Key Fragment in the Polyhydroxylated Chain Common to Oscillariolide and Phormidolides A-CAlejandro Gil, Janire Lamariano-Merketegi, Adriana Lorente, et al.
The Journal of Organic Chemistry|January 24, 1997
Total Synthesis of Dehydrodidemnin B. Use of Uronium and Phosphonium Salt Coupling Reagents in Peptide Synthesis in SolutionGemma Jou, Isabel González, Fernando Albericio, et al.
Molecular Pharmaceutics|August 19, 2010
The antitumoral depsipeptide IB-01212 kills Leishmania through an apoptosis-like process involving intracellular targetsJuan R Luque-Ortega, Luis J Cruz, Fernando Albericio, et al.
The Journal of Organic Chemistry|November 25, 2010
Isolation, structural assignment, and total synthesis of barmumycinAdriana Lorente, Daniel Pla, Librada M Cañedo, et al.
Journal of Peptide Science : an Official Publication of the European Peptide Society|November 19, 2013
Inhibitory effect of short cationic homopeptides against gram-positive bacteriaFanny Guzmán, Sergio Marshall, Claudia Ojeda, et al.
Journal of Peptide Science : an Official Publication of the European Peptide Society|May 29, 2013
COMU: scope and limitations of the latest innovation in peptide acyl transfer reagentsRamon Subirós-Funosas, Lidia Nieto-Rodriguez, Knud J Jensen, et al.
Chemmedchem|April 3, 2008
Use of N-methylpiperazine for the preparation of piperazine-based unsymmetrical bis-ureas as anti-HIV agentsAyman El-Faham, Mercedes Armand-Ugón, Jose A Esté, et al.
Organic Letters|March 15, 2019
Pseudo-Wang Handle for the Preparation of Fully Protected Peptides. Synthesis of Liraglutide by Fragment CondensationDaniel Carbajo, Peter Fransen, Ayman El-Faham, et al.
Chemistry (Weinheim an Der Bergstrasse, Germany)|July 4, 2009
Oxyma: an efficient additive for peptide synthesis to replace the benzotriazole-based HOBt and HOAt with a lower risk of explosionRamon Subirós-Funosas, Rafel Prohens, Rafael Barbas, et al.
The Journal of Organic Chemistry|August 30, 2008
THAL, a sterically unhindered linker for the solid-phase synthesis of acid-sensitive protected peptide acidsAlbert Isidro-Llobet, Ulrik Boas, Knud J Jensen, et al.
Pageof 53