Synthesis of 2-Imino-1,3,4-oxadiazolines from Acylhydrazides and Isothiocyanates via Aerobic Oxidation and a DMAP-Mediated Annulation Sequence-Reference-Cited by-同舟云学术

Synthesis of 2-Imino-1,3,4-oxadiazolines from Acylhydrazides and Isothiocyanates via Aerobic Oxidation and a DMAP-Mediated Annulation Sequence

Published:2022-08-01 Issue:32 Volume:7 Page:28148-28159
ISSN:2470-1343
Container-title:ACS Omega
language:en
Short-container-title:ACS Omega

Author:

Lim Jae Hyeok¹,Baek Sang Eun¹,Lad Bapurao Sudam¹,Kim Jinho¹^ORCID

Affiliation:

1. Department of Chemistry, and Research Institute of Basic Sciences, Incheon National University, 119 Academy-ro, Yeonsu-gu, Incheon 22012, Republic of Korea

Funder

National Research Foundation of Korea

Incheon National University

Publisher

American Chemical Society (ACS)

Subject

General Chemical Engineering,General Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acsomega.2c02323

Reference44 articles.

1. Triphenylamines and 1,3,4-oxadiazoles: a versatile combination for controlling the charge balance in organic electronics

2. 1,3,4-Oxadiazoles as luminescent materials for organic light emitting diodes via cross-coupling reactions

3. Blue light‐emitting organic electroluminescent devices

4. Intramolecular Diels−Alder and Tandem Intramolecular Diels−Alder/1,3-Dipolar Cycloaddition Reactions of 1,3,4-Oxadiazoles

5. Intramolecular Diels−Alder/1,3-Dipolar Cycloaddition Cascade of 1,3,4-Oxadiazoles

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