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Luca Banfi

Showing results (11-20 of 51) with videos related to

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Organic & Biomolecular Chemistry|December 26, 2008
A novel intramolecular Ugi reaction with 7-azabicyclo[2.2.1]heptane derivatives followed by post-condensation acylations: a new entry to azanorbornyl peptidomimeticsAndrea Basso, Luca Banfi, Giuseppe Guanti, et al.
Organic & Biomolecular Chemistry|April 29, 2005
Asymmetrized tris(hydroxymethyl)methane as a precursor of N- and O-containing 6-membered heterocycles through ring-closing metathesisLuca Banfi, Giuseppe Guanti, Monica Paravidino, et al.
Organic & Biomolecular Chemistry|February 4, 2011
A new diversity oriented and metal-free approach to highly functionalized 3H-pyrimidin-4-onesRenata Riva, Luca Banfi, Andrea Basso, et al.
The Journal of Organic Chemistry|January 18, 2005
A novel highly selective chiral auxiliary for the asymmetric synthesis of L- and D-alpha-amino acid derivatives via a multicomponent Ugi reactionAndrea Basso, Luca Banfi, Renata Riva, et al.
Combinatorial Chemistry & High Throughput Screening|May 24, 2011
Beyond Ugi and Passerini reactions: multicomponent approaches based on isocyanides and alkynes as an efficient tool for diversity oriented synthesisFabio De Moliner, Luca Banfi, Renata Riva, et al.
Chemical Science|January 10, 2022
The 100 facets of the Passerini reactionLuca Banfi, Andrea Basso, Chiara Lambruschini, et al.
Molecular Diversity|September 3, 2008
Multicomponent synthesis of benzoxazinones via tandem Ugi/Mitsunobu reactions: an unexpected cine-substitutionLuca Banfi, Andrea Basso, Giuseppe Guanti, et al.
The Journal of Organic Chemistry|January 16, 2008
Polyfunctionalized pyrrolidines by Ugi multicomponent reaction followed by palladium-mediated SN2' cyclizationsLuca Banfi, Andrea Basso, Valentina Cerulli, et al.
Organic & Biomolecular Chemistry|January 5, 2012
Diversity oriented and chemoenzymatic synthesis of densely functionalized pyrrolidines through a highly diastereoselective Ugi multicomponent reactionValentina Cerulli, Luca Banfi, Andrea Basso, et al.
Chemistry (Weinheim an Der Bergstrasse, Germany)|February 14, 2013
The homo-PADAM protocol: stereoselective and operationally simple synthesis of α-oxo- or α-hydroxy-γ-acylaminoamides and chromanesFabio Morana, Andrea Basso, Renata Riva, et al.
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Showing results (11-20 of 51) with videos related to

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Pageof 6
Organic & Biomolecular Chemistry|December 26, 2008
A novel intramolecular Ugi reaction with 7-azabicyclo[2.2.1]heptane derivatives followed by post-condensation acylations: a new entry to azanorbornyl peptidomimeticsAndrea Basso, Luca Banfi, Giuseppe Guanti, et al.
Organic & Biomolecular Chemistry|April 29, 2005
Asymmetrized tris(hydroxymethyl)methane as a precursor of N- and O-containing 6-membered heterocycles through ring-closing metathesisLuca Banfi, Giuseppe Guanti, Monica Paravidino, et al.
Organic & Biomolecular Chemistry|February 4, 2011
A new diversity oriented and metal-free approach to highly functionalized 3H-pyrimidin-4-onesRenata Riva, Luca Banfi, Andrea Basso, et al.
The Journal of Organic Chemistry|January 18, 2005
A novel highly selective chiral auxiliary for the asymmetric synthesis of L- and D-alpha-amino acid derivatives via a multicomponent Ugi reactionAndrea Basso, Luca Banfi, Renata Riva, et al.
Combinatorial Chemistry & High Throughput Screening|May 24, 2011
Beyond Ugi and Passerini reactions: multicomponent approaches based on isocyanides and alkynes as an efficient tool for diversity oriented synthesisFabio De Moliner, Luca Banfi, Renata Riva, et al.
Chemical Science|January 10, 2022
The 100 facets of the Passerini reactionLuca Banfi, Andrea Basso, Chiara Lambruschini, et al.
Molecular Diversity|September 3, 2008
Multicomponent synthesis of benzoxazinones via tandem Ugi/Mitsunobu reactions: an unexpected cine-substitutionLuca Banfi, Andrea Basso, Giuseppe Guanti, et al.
The Journal of Organic Chemistry|January 16, 2008
Polyfunctionalized pyrrolidines by Ugi multicomponent reaction followed by palladium-mediated SN2' cyclizationsLuca Banfi, Andrea Basso, Valentina Cerulli, et al.
Organic & Biomolecular Chemistry|January 5, 2012
Diversity oriented and chemoenzymatic synthesis of densely functionalized pyrrolidines through a highly diastereoselective Ugi multicomponent reactionValentina Cerulli, Luca Banfi, Andrea Basso, et al.
Chemistry (Weinheim an Der Bergstrasse, Germany)|February 14, 2013
The homo-PADAM protocol: stereoselective and operationally simple synthesis of α-oxo- or α-hydroxy-γ-acylaminoamides and chromanesFabio Morana, Andrea Basso, Renata Riva, et al.
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