Experimental and Computational Studies of Microwave-Assisted, Facile Ring Opening of Epoxide with Less Reactive Aromatic Amines in Nitromethane-Reference-Cited by-同舟云学术

Experimental and Computational Studies of Microwave-Assisted, Facile Ring Opening of Epoxide with Less Reactive Aromatic Amines in Nitromethane

Published:2020-07-21 Issue:30 Volume:5 Page:18746-18757
ISSN:2470-1343
Container-title:ACS Omega
language:en
Short-container-title:ACS Omega

Author:

Kumar Sumit¹,Upadhyay Charu¹,Bansal Meenakshi²,Grishina Maria³,Chhikara Bhupender S.⁴,Potemkin Vladimir³,Rathi Brijesh²³^ORCID,Poonam ¹³^ORCID

Affiliation:

1. Department of Chemistry, Miranda House, University of Delhi, Delhi 110007, India

2. Laboratory for Translational Chemistry and Drug Discovery, Department of Chemistry, Hansraj College University Enclave, University of Delhi, Delhi 110007, India

3. Laboratory of Computational Modelling of Drugs, South Ural State University, Chelyabinsk 454080, Russia

4. Department of Chemistry, Aditi Mahavidyalaya, University of Delhi, Bawana, Delhi 110039, India

Funder

Council of Scientific and Industrial Research

Department of Science and Technology, Ministry of Science and Technology

Government of the Russian Federation

Ministry of Science and Higher Education of the Russian Federation

Publisher

American Chemical Society (ACS)

Subject

General Chemical Engineering,General Chemistry

Link

http://pubs.acs.org/doi/pdf/10.1021/acsomega.0c01760

Reference49 articles.

1. Characterization of the Epoxide Hydrolase NcsF2 from the Neocarzinostatin Biosynthetic Gene Cluster

2. Epoxide Ring-Opening Reactions with Mesoporous Silica-Supported Fe(III) Catalysts

3. Template Assisted Synthesis of Nanocrystalline Sulfated Titania: Active and Robust Catalyst for Regioselective Ring Opening of Epoxide with Aniline and Kinetic Modeling

4. re- andsi-Face-Selective Nitroaldol Reactions Catalyzed by a Rigid Chiral Quaternary Ammonium Salt: A Highly Stereoselective Synthesis of the HIV Protease Inhibitor Amprenavir (Vertex 478)

5. Fast-Acting Small Molecules Targeting Malarial Aspartyl Proteases, Plasmepsins, Inhibit Malaria Infection at Multiple Life Stages

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