Zobrazeno 1 - 10
of 24
pro vyhledávání: '"Alejandro A, Orden"'
Autor:
Florencia Carmona-Viglianco, Daniel Zaragoza-Puchol, Gabriela E. Feresin, Fabricio R. Bisogno, Marcela Kurina-Sanz, Alejandro A. Orden
Publikováno v:
Phytochemistry Letters. 51:5-11
Autor:
Patricia A. Lucero, Cynthia Magallanes-Noguera, Fernando A. Giannini, Mirtha Nassetta, Alejandro A. Orden, Marcela Kurina-Sanz
Publikováno v:
International Journal of Phytoremediation. 25:106-114
Although many countries banned the insecticide endosulfan, it is still an environmental pollutant. Plants metabolize the two diastereomers of the formulations known as technical grade endosulfan (TGE) by two phase I pathways: hydrolysis leading to le
Autor:
Daniel Zaragoza-Puchol, Javier E. Ortiz, Alejandro A. Orden, Marianela Sanchez, Jorge Palermo, Alejandro Tapia, Jaume Bastida, Gabriela E. Feresin
Publikováno v:
Molecules, Vol 26, Iss 1, p 192 (2021)
Plants in the Amaryllidaceae family synthesize a diversity of bioactive alkaloids. Some of these plant species are not abundant and have a low natural multiplication rate. The aims of this work were the alkaloids analysis of a Habranthus cardenasianu
Externí odkaz:
https://doaj.org/article/69f161d8ad1d4b9ea3157b8a4d948e14
Autor:
Celeste Aguirre-Pranzoni, Marcela Kurina-Sanz, Alejandro A. Orden, Fabricio R. Bisogno, Rodrigo D. Tosso
Publikováno v:
CONICET Digital (CONICET)
Consejo Nacional de Investigaciones Científicas y Técnicas
instacron:CONICET
Consejo Nacional de Investigaciones Científicas y Técnicas
instacron:CONICET
Chemoenzymatic strategies for the preparation of enantiopure β-hydroxytriazoles were designed. These and other related compounds are particularly relevant because of their antitubercular bioactivities and as β-adrenergic receptor blockers. The abil
Autor:
Jorge Alejandro Palermo, Alejandro Tapia, Javier E. Ortiz, Daniel Zaragoza-Puchol, Gabriela Egly Feresin, Marianela Sánchez, Jaume Bastida, Alejandro A. Orden
Publikováno v:
Dipòsit Digital de la UB
Universidad de Barcelona
Molecules
Volume 26
Issue 1
Molecules, Vol 26, Iss 192, p 192 (2021)
Universidad de Barcelona
Molecules
Volume 26
Issue 1
Molecules, Vol 26, Iss 192, p 192 (2021)
Plants in the Amaryllidaceae family synthesize a diversity of bioactive alkaloids. Some of these plant species are not abundant and have a low natural multiplication rate. The aims of this work were the alkaloids analysis of a Habranthus cardenasianu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1d9aa146471e0c471f189341ce33b0c8
http://hdl.handle.net/2445/184412
http://hdl.handle.net/2445/184412
Autor:
Daniel, Zaragoza-Puchol, Javier E, Ortiz, Alejandro A, Orden, Marianela, Sanchez, Jorge, Palermo, Alejandro, Tapia, Jaume, Bastida, Gabriela E, Feresin
Publikováno v:
Molecules
Plants in the Amaryllidaceae family synthesize a diversity of bioactive alkaloids. Some of these plant species are not abundant and have a low natural multiplication rate. The aims of this work were the alkaloids analysis of a Habranthus cardenasianu
Autor:
Adriana Garro, Gabriela Egly Feresin, Alejandro A. Orden, Florencia Carmona-Viglianco, Daniel Zaragoza-Puchol, Oscar Parravicini, Marcela Kurina-Sanz, Ricardo D. Enriz
Publikováno v:
CONICET Digital (CONICET)
Consejo Nacional de Investigaciones Científicas y Técnicas
instacron:CONICET
Consejo Nacional de Investigaciones Científicas y Técnicas
instacron:CONICET
In this work, we report the synthesis of a series of derivatives of N-benzyl-2-phenylethanamine which is the framework of norbelladine, the natural common precursor of the Amaryllidaceae alkaloids. These compounds were assessed in the inhibition of b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2c61ab102d2192a0d0eed73e6311642a
https://pubs.rsc.org/en/content/articlelanding/2020/NJ/D0NJ00282H
https://pubs.rsc.org/en/content/articlelanding/2020/NJ/D0NJ00282H
Autor:
María Laura Mascotti, Alejandro A. Orden, Elizabeth Agostini, Cynthia Magallanes-Noguera, Francisco M. Cecati, Marcela Kurina-Sanz, Guillermo Federico Reta
Publikováno v:
CONICET Digital (CONICET)
Consejo Nacional de Investigaciones Científicas y Técnicas
instacron:CONICET
Consejo Nacional de Investigaciones Científicas y Técnicas
instacron:CONICET
While many redox enzymes are nowadays available for synthetic applications, the toolbox of ene-reductases is still limited. Consequently, the screening for these enzymes from diverse sources in the search of new biocatalyst suitable for green chemist
Publikováno v:
Journal of Molecular Catalysis B: Enzymatic. 114:19-24
Rhodotorula sp. LSL, isolated from a local landfarming was able to catalyze the reduction of prochiral arylketones into sec-alcohols with excellent Prelog stereoselectivity (ee > 99%). The use of resting and lyophilized cells was optimized accessing
Publikováno v:
Current Organic Chemistry. 16:2598-2612
Oxidative enzymes constitute privileged catalysts in organic synthesis. Environmentally benign reaction conditions along with high selectivity are the most appealing characteristic shown by these biocatalysts in contrast to classical metal-based reag