Catalyst‐Free Regioselective [3+2] Cycloadditions of α,β‐unsaturated N ‐arylnitrones with Alkenes to Access Functionalized Isoxazolidines: A DFT Study-Reference-Cited by-同舟云学术

Catalyst‐Free Regioselective [3+2] Cycloadditions of α,β‐unsaturated N ‐arylnitrones with Alkenes to Access Functionalized Isoxazolidines: A DFT Study

Published:2020-02-24 Issue:6 Volume:15 Page:899-903
ISSN:1861-4728
Container-title:Chemistry – An Asian Journal
language:en
Short-container-title:Chem. Asian J.

Author:

Ghosh Arnab¹,Mane Manoj V.²³,Rode Haridas B.⁴⁵,Patil Siddappa A.¹,Sridhar Balasubramanian⁶,Dateer Ramesh B.¹^ORCID

Affiliation:

1. Centre for Nano and Material SciencesJain University Jain Global Campus Bangalore Karnataka 562112 India

2. Physical Chemistry DivisionCSIR – National Chemical Laboratory Dr. Homi Bhabha Road Pune 411 008 India

3. KAUST Catalysis CentreKing Abdullah University of Science and Technology (KAUST) Thuwal 23955-6900 Saudi Arabia

4. Department of Organic Synthesis and Process ChemistryCSIR-Indian Institute of Chemical Technology Tarnaka Hyderabad Telangana 500007 India

5. Academy of Scientific and Innovative Research Ghaziabad Uttar Pradesh 201 002 India

6. Center for X-ray crystallography Analytical DepartmentCSIR-Indian Institute of Chemical Technology Tarnaka Hyderabad Telangana 500007 India

Publisher

Wiley

Subject

General Chemistry,Biochemistry,Organic Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/asia.201901754

Reference89 articles.

2. Copper-Catalyzed Rearrangement ofN-Aryl Nitrones into Epoxyketimines

3. Copper-Catalyzed Rearrangement ofN-Aryl Nitrones into Epoxyketimines

4. Zinc Triflate Catalyzed Aerobic Cross-Dehydrogenative Coupling (CDC) of Alkynes with Nitrones: A New Entry to Isoxazoles

5. Synthesis of N-Styrenyl Amidines from α,β-Unsaturated Nitrones and Isocyanates through CO2 Elimination and Styrenyl Migration

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