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Marcus M Sá

Showing results (1-10 of 16) with videos related to

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The Journal of Organic Chemistry|April 25, 2014
Lithium chloride-mediated stereoselective synthesis of cyclopropanecarboxamides from γ,δ-epoxy malonates through a domino cyclopropanation/lactonization/aminolysis processMarcelo V Marques, Marcus M Sá
Acta Crystallographica. Section E, Crystallographic Communications|March 21, 2017
Crystal structure of 5-<i>O</i>-benzoyl-2,3-<i>O</i>-iso-propyl-idene-d-ribono-1,4-lactoneAdailton J Bortoluzzi, Gustavo P Silveira, Marcus M Sá
The Journal of Organic Chemistry|January 4, 2011
Nucleophilic ring-opening of epoxide and aziridine acetates for the stereodivergent synthesis of β-hydroxy and β-amino γ-lactamsTula B Bisol, Adailton J Bortoluzzi, Marcus M Sá
Acta Crystallographica. Section E, Structure Reports Online|May 18, 2011
(E,E)-Methyl 2-[(3-nitrobenzylidene)-aminomethyl]-3-phenylpropenoateAdailton J Bortoluzzi, Tula B Bisol, Marcus M Sá
Acta Crystallographica. Section E, Structure Reports Online|November 8, 2011
5-O-Acetyl-d-ribono-1,4-lactoneAdailton J Bortoluzzi, Damianni Sebrão, Marcus M Sá, et al.
Molecules (Basel, Switzerland)|February 26, 2020
Stereoselective Bioreduction of α-diazo-β-keto EstersSergio González-Granda, Taíssa A Costin, Marcus M Sá, et al.
Beilstein Journal of Organic Chemistry|March 10, 2018
Continuous multistep synthesis of 2-(azidomethyl)oxazolesThaís A Rossa, Nícolas S Suveges, Marcus M Sá, et al.
Bioorganic & Medicinal Chemistry Letters|August 1, 2008
Metal-free artificial nucleases based on simple oxime and hydroxylamine scaffoldsLuciano Fernandes, Franciele L Fischer, Carolina W Ribeiro, et al.
Chemistry, an Asian Journal|February 14, 2025
Regiodivergent Synthesis of α- and β-Acyloxy Acrylates through Catalyst-Driven Migrations from α-Diazo-β-Acyloxy EstersGabriela M Diogo, Pedro A M Moro, Vinicius C Port, et al.
Organic & Biomolecular Chemistry|July 26, 2011
Mechanism of intramolecular catalysis in the hydrolysis of alkyl monoesters of 1,8-naphthalic acidBruno S Souza, Santiago F Yunes, Marcelo F Lima, et al.
Pageof 2

Showing results (1-10 of 16) with videos related to

Sort By:
Pageof 2
The Journal of Organic Chemistry|April 25, 2014
Lithium chloride-mediated stereoselective synthesis of cyclopropanecarboxamides from γ,δ-epoxy malonates through a domino cyclopropanation/lactonization/aminolysis processMarcelo V Marques, Marcus M Sá
Acta Crystallographica. Section E, Crystallographic Communications|March 21, 2017
Crystal structure of 5-<i>O</i>-benzoyl-2,3-<i>O</i>-iso-propyl-idene-d-ribono-1,4-lactoneAdailton J Bortoluzzi, Gustavo P Silveira, Marcus M Sá
The Journal of Organic Chemistry|January 4, 2011
Nucleophilic ring-opening of epoxide and aziridine acetates for the stereodivergent synthesis of β-hydroxy and β-amino γ-lactamsTula B Bisol, Adailton J Bortoluzzi, Marcus M Sá
Acta Crystallographica. Section E, Structure Reports Online|May 18, 2011
(E,E)-Methyl 2-[(3-nitrobenzylidene)-aminomethyl]-3-phenylpropenoateAdailton J Bortoluzzi, Tula B Bisol, Marcus M Sá
Acta Crystallographica. Section E, Structure Reports Online|November 8, 2011
5-O-Acetyl-d-ribono-1,4-lactoneAdailton J Bortoluzzi, Damianni Sebrão, Marcus M Sá, et al.
Molecules (Basel, Switzerland)|February 26, 2020
Stereoselective Bioreduction of α-diazo-β-keto EstersSergio González-Granda, Taíssa A Costin, Marcus M Sá, et al.
Beilstein Journal of Organic Chemistry|March 10, 2018
Continuous multistep synthesis of 2-(azidomethyl)oxazolesThaís A Rossa, Nícolas S Suveges, Marcus M Sá, et al.
Bioorganic & Medicinal Chemistry Letters|August 1, 2008
Metal-free artificial nucleases based on simple oxime and hydroxylamine scaffoldsLuciano Fernandes, Franciele L Fischer, Carolina W Ribeiro, et al.
Chemistry, an Asian Journal|February 14, 2025
Regiodivergent Synthesis of α- and β-Acyloxy Acrylates through Catalyst-Driven Migrations from α-Diazo-β-Acyloxy EstersGabriela M Diogo, Pedro A M Moro, Vinicius C Port, et al.
Organic & Biomolecular Chemistry|July 26, 2011
Mechanism of intramolecular catalysis in the hydrolysis of alkyl monoesters of 1,8-naphthalic acidBruno S Souza, Santiago F Yunes, Marcelo F Lima, et al.
Pageof 2