Conformational and Stereodynamic Behavior of Five- to Seven-Membered 1-Aryl-2-iminoazacycloalkanes-Reference-Cited by-同舟云学术

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

Published:2019-03-04 Issue:3 Volume:4 Page:4712-4720
ISSN:2470-1343
Container-title:ACS Omega
language:en
Short-container-title:ACS Omega

Author:

Díaz Jimena E.¹²,Mazzanti Andrea¹^ORCID,Orelli Liliana R.²^ORCID,Mancinelli Michele¹^ORCID

Affiliation:

1. Department of Industrial Chemistry “Toso Montanari”, University of Bologna, Viale Risorgimento 4, 40136 Bologna, Italy

2. Departamento de Química Orgánica. Facultad de Farmacia y Bioquímica, Universidad de Buenos Aires. CONICET, Junín 956, 1113 Buenos Aires, Argentina

Funder

Universidad de Buenos Aires

Universit? di Bologna

Publisher

American Chemical Society (ACS)

Subject

General Chemical Engineering,General Chemistry

Link

http://pubs.acs.org/doi/pdf/10.1021/acsomega.9b00192

Reference38 articles.

1. Importance and synthesis of benzannulated medium-sized and macrocyclic rings (BMRs)

2. Analysis of the Structural Diversity, Substitution Patterns, and Frequency of Nitrogen Heterocycles among U.S. FDA Approved Pharmaceuticals

3. 2-Iminopyrrolidines as Potent and Selective Inhibitors of Human Inducible Nitric Oxide Synthase

4. Microwave-assisted cyclizations promoted by polyphosphoric acid esters: a general method for 1-aryl-2-iminoazacycloalkanes

5. Atropisomerism and Axial Chirality in Heteroaromatic Compounds

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