3-Nitroatenolol: First Synthesis, Chiral Resolution and Enantiomers’ Absolute Configuration
3-Nitroatenolol: First Synthesis, Chiral Resolution and Enantiomers’ Absolute Configuration
About this item
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Author / Creator
Sparaco, Rosa , Cinque, Pierfrancesco , Scognamiglio, Antonia , Corvino, Angela , Caliendo, Giuseppe , Fiorino, Ferdinando , Magli, Elisa , Perissutti, Elisa , Santagada, Vincenzo , Severino, Beatrice , Luciano, Paolo , Casertano, Marcello , Aiello, Anna , Martins Viegas, Gustavo Yuri , De Nucci, Gilberto and Frecentese, Francesco
Publisher
Switzerland: MDPI AG
Journal title
Language
English
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Publication information
Publisher
Switzerland: MDPI AG
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Scope and Contents
Contents
4-Nitro and 7-nitro propranolol have been recently synthesized and characterized by us. (±)-4-NO2-propranolol has been shown to act as a selective antagonist of 6-nitrodopamine (6-ND) receptors in the right atrium of rats. As part of our follow-up to this study, herein, we describe the first synthesis of (±)-3-nitroatenolol as a probe to evaluate t...
Alternative Titles
Full title
3-Nitroatenolol: First Synthesis, Chiral Resolution and Enantiomers’ Absolute Configuration
Authors, Artists and Contributors
Author / Creator
Cinque, Pierfrancesco
Scognamiglio, Antonia
Corvino, Angela
Caliendo, Giuseppe
Fiorino, Ferdinando
Magli, Elisa
Perissutti, Elisa
Santagada, Vincenzo
Severino, Beatrice
Luciano, Paolo
Casertano, Marcello
Aiello, Anna
Martins Viegas, Gustavo Yuri
De Nucci, Gilberto
Frecentese, Francesco
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Primary Identifiers
Record Identifier
TN_cdi_doaj_primary_oai_doaj_org_article_1faca57576ae452e9550a466612b7446
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_1faca57576ae452e9550a466612b7446
Other Identifiers
ISSN
1420-3049
E-ISSN
1420-3049
DOI
10.3390/molecules29071598
