Aerobic oxidative esterification and thioesterification of aldehydes using dibromoisocyanuric acid under mild conditions: no metal catalysts required-Reference-Cited by-同舟云学术

Aerobic oxidative esterification and thioesterification of aldehydes using dibromoisocyanuric acid under mild conditions: no metal catalysts required

Published:2018 Issue:13 Volume:42 Page:10833-10841
ISSN:1144-0546
Container-title:New Journal of Chemistry
language:en
Short-container-title:New J. Chem.

Author:

Kwon Young-Do¹²³⁴⁵,La Minh Thanh⁶⁷⁸⁹⁵,Kim Hee-Kwon⁶⁷⁸⁹⁵^ORCID

Affiliation:

1. School of Energy

2. Materials & Chemical Engineering

3. Korea University of Technology and Education

4. Cheonan 31253

5. Republic of Korea

6. Department of Nuclear Medicine

7. Molecular Imaging & Therapeutic Medicine Research Center

8. Chonbuk National University Medical School and Hospital

9. Jeonju 54907

Abstract

Esters and thioesters were successfully prepared through oxidative esterification and thioesterification of corresponding aldehydes in the presence of dibromoisocyanuric acid.

Funder

National Research Foundation of Korea

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,General Chemistry,Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2018/NJ/C8NJ01085D

Reference45 articles.

1. The design and synthesis of the Angiotensin Converting Enzyme inhibitor Cilazapril and related bicyclic compounds

2. Synthesis of Amide and Ester Derivatives of Cinnamic Acid and Its Analogs: Evaluation of Their Free Radical Scavenging and Monoamine Oxidase and Cholinesterase Inhibitory Activities

3. Design, Synthesis, and Evaluation of Novel Phenolic Acid/Dipeptide/Borneol Hybrids as Potent Angiotensin Converting Enzyme (ACE) Inhibitors with Anti-hypertension Activity

4. Indole carboxylic acid esters of melampomagnolide B are potent anticancer agents against both hematological and solid tumor cells

5. Discovery of novel antitumor nitric oxide-donating β -elemene hybrids through inhibiting the PI3K/Akt pathway

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