Conformational and Stereodynamic Behavior of Five- to Seven-Membered 1‑Aryl-2-iminoazacycloalkanes

Autor: Jimena E. Díaz, Andrea Mazzanti, Liliana R. Orelli, Michele Mancinelli

Publikováno v: ACS Omega, Vol 4, Iss 3, Pp 4712-4720 (2019)

Externí odkaz: https://doaj.org/article/fd36a7bc68b4405ea211a9ec64d482a9

Syntheses of 3,4- and 1,4-dihydroquinazolines from 2-aminobenzylamine

Autor: Jimena E. Díaz, Silvia Ranieri, Nadia Gruber, Liliana R. Orelli

Publikováno v: Beilstein Journal of Organic Chemistry, Vol 13, Iss 1, Pp 1470-1477 (2017)

A straightforward strategy for the synthesis of dihydroquinazolines is presented, which allows for the preparation of 3,4- and 1,4-dihydroquinazolines with different substitution patterns from 2-aminobenzylamine (2-ABA) as common precursor. The requi

Externí odkaz: https://doaj.org/article/c3834671f5b44f71b4b83845605e28e8

Polyphosphoric Acid Esters Promoted Synthesis of Quinazolin-4(3H)-imines from 2-Aminobenzonitrile

Autor: Natalia B. Kilimciler, Nicolás M. Palavecino, Nadia Gruber, Daniel R. Vega, Liliana R. Orelli, Jimena E. Díaz

Publikováno v: The Journal of Organic Chemistry.

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::e3e2d9200b53e9896d711f311ee6d9b6
https://doi.org/10.1021/acs.joc.2c02558

Microwave-assisted synthesis of 2-substituted 4,5,6,7-tetrahydro-1,3-thiazepines from 4-aminobutanol

Autor: Natalia B. Kilimciler, Liliana R. Orelli, Juan A. Bisceglia, Maria C. Mollo

Publikováno v: Beilstein Journal of Organic Chemistry, Vol 16, Iss 1, Pp 32-38 (2020)
Beilstein Journal of Organic Chemistry

A general procedure for the synthesis of 2-substituted tetrahydro-1,3-thiazepines by MW-assisted cyclization of 4-thioamidobutanols is presented. The acyclic precursors were prepared in high overall yields by an expeditious three-step diacylation/thi

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::78d8aadf834a092fe42ffce48f4f0205
https://doaj.org/article/028000be7c1247eeadf68e6c327fe697

Amidinoquinoxaline-Based Nitrones as Lipophilic Antioxidants

Autor: Liliana R. Orelli, Pierluigi Stipa, Nadia Gruber, Cristina Minnelli, Giovanna Mobbili, Emiliano Laudadio, Luca Mangano

Publikováno v: Antioxidants
Volume 10
Issue 8
Antioxidants, Vol 10, Iss 1185, p 1185 (2021)
CONICET Digital (CONICET)
Consejo Nacional de Investigaciones Científicas y Técnicas
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The potential of nitrones (N-oxides) as therapeutic antioxidants is due to their ability to counteract oxidative stress, mainly attributed to their action as radical scavengers toward C- and O-centered radicals. Among them, nitrones from the amidinoq

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1458e71742d6dc022e5fcd1f1b4b905c