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Acta Crystallographica. Section C, Crystal Structure Communications
|
April 5, 2002
Reactive intermediates in peptide synthesis. ortho-Nitrophenyl Nalpha-para-toluenesulfonyl-alpha-aminoisobutyrate
Marco Crisma, Claudio Toniolo
Acta Crystallographica. Section C, Crystal Structure Communications
|
May 2, 2002
Reactive intermediates in peptide synthesis: the N-oxysuccinimido ester of Nalpha-para-toluenesulfonyl-alpha-aminoisobutyric acid
Marco Crisma, Claudio Toniolo
Biopolymers
|
November 4, 2014
Helical screw-sense preferences of peptides based on chiral, Cα-tetrasubstituted α-amino acids
Marco Crisma, Claudio Toniolo
Organic Letters
|
May 16, 2019
Tunable E- Z Photoisomerization in α,β-Peptide Foldamers Featuring Multiple ( E/ Z)-3-Aminoprop-2-enoic Acid Units
Giulia Marafon, Marco Crisma, Alessandro Moretto
Angewandte Chemie (International Ed. in English)
|
June 27, 2018
Intrinsically Photoswitchable α/β Peptides toward Two-State Foldamers
Giulia Marafon, Marco Crisma, Alessandro Moretto
Biomolecular Concepts
|
December 2, 2014
Peptide-based rotaxanes and catenanes: an emerging class of supramolecular chemistry systems
Alessandro Moretto, Marco Crisma, Fernando Formaggio, et al.
Biopolymers
|
May 9, 2006
Handedness control of peptide helices by amino acid side-chain chirality: Ile/aIle peptides
Erika Andreetto, Cristina Peggion, Marco Crisma, et al.
Chempluschem
|
January 25, 2020
Azacrown Ethers from Mustard Carbonate Analogues
Fabio Aricò, Ilina Udrea, Marco Crisma, et al.
Biopolymers
|
August 27, 2005
Peptide helices based on alpha-amino acids
Marco Crisma, Fernando Formaggio, Alessandro Moretto, et al.
Biopolymers
|
June 22, 2010
Building a bridge between peptide chemistry and organic chemistry: intramolecular macrocyclization reactions and supramolecular chemistry with helical peptide substrates
Alessandro Moretto, Marco Crisma, Fernando Formaggio, et al.
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of 12
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Showing results (1-10 of 111) with videos related to
Sort By:
Page
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Acta Crystallographica. Section C, Crystal Structure Communications
|
April 5, 2002
Reactive intermediates in peptide synthesis. ortho-Nitrophenyl Nalpha-para-toluenesulfonyl-alpha-aminoisobutyrate
Marco Crisma, Claudio Toniolo
Acta Crystallographica. Section C, Crystal Structure Communications
|
May 2, 2002
Reactive intermediates in peptide synthesis: the N-oxysuccinimido ester of Nalpha-para-toluenesulfonyl-alpha-aminoisobutyric acid
Marco Crisma, Claudio Toniolo
Biopolymers
|
November 4, 2014
Helical screw-sense preferences of peptides based on chiral, Cα-tetrasubstituted α-amino acids
Marco Crisma, Claudio Toniolo
Organic Letters
|
May 16, 2019
Tunable E- Z Photoisomerization in α,β-Peptide Foldamers Featuring Multiple ( E/ Z)-3-Aminoprop-2-enoic Acid Units
Giulia Marafon, Marco Crisma, Alessandro Moretto
Angewandte Chemie (International Ed. in English)
|
June 27, 2018
Intrinsically Photoswitchable α/β Peptides toward Two-State Foldamers
Giulia Marafon, Marco Crisma, Alessandro Moretto
Biomolecular Concepts
|
December 2, 2014
Peptide-based rotaxanes and catenanes: an emerging class of supramolecular chemistry systems
Alessandro Moretto, Marco Crisma, Fernando Formaggio, et al.
Biopolymers
|
May 9, 2006
Handedness control of peptide helices by amino acid side-chain chirality: Ile/aIle peptides
Erika Andreetto, Cristina Peggion, Marco Crisma, et al.
Chempluschem
|
January 25, 2020
Azacrown Ethers from Mustard Carbonate Analogues
Fabio Aricò, Ilina Udrea, Marco Crisma, et al.
Biopolymers
|
August 27, 2005
Peptide helices based on alpha-amino acids
Marco Crisma, Fernando Formaggio, Alessandro Moretto, et al.
Biopolymers
|
June 22, 2010
Building a bridge between peptide chemistry and organic chemistry: intramolecular macrocyclization reactions and supramolecular chemistry with helical peptide substrates
Alessandro Moretto, Marco Crisma, Fernando Formaggio, et al.
Page
of 12