Aerobic oxidative acylation of nitroarenes with arylacetic esters under mild conditions: facile access to diarylketones-Reference-Cited by-同舟云学术

Aerobic oxidative acylation of nitroarenes with arylacetic esters under mild conditions: facile access to diarylketones

Published:2018 Issue:1 Volume:16 Page:140-145
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Li Jiang-Sheng¹²³⁴⁵^ORCID,Yang Qian¹²³⁴⁵,Yang Fan⁶⁷⁵¹²,Chen Guo-Qin¹²³⁴⁵,Li Zhi-Wei¹²³⁴⁵,Kuang Yin-Jie¹²³⁴⁵,Zhang Wei-Jing¹²³⁴⁵,Huang Peng-Mian¹²³⁴⁵

Affiliation:

1. Hunan Provincial Key Laboratory of Materials Protection for Electric Power and Transportation

2. School of Chemistry and Biological Engineering

3. Changsha University of Science & Technology

4. Changsha 410114

5. P.R. China

6. SINOPEC Baling Petrochemical Company

7. Yueyang 414014

Abstract

A regioselectivet-BuONa-mediated aerobic oxidative acylation of nitroarenes under mild conditions is developed through a cascade CDC/oxidative decarboxylation process.

Funder

National Natural Science Foundation of China

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2018/OB/C7OB02865B

Reference50 articles.

1. Organocatalysis in Inert C–H Bond Functionalization

2. Oxidative C–H/C–H Coupling Reactions between Two (Hetero)arenes

3. From C(sp2)–H to C(sp3)–H: systematic studies on transition metal-catalyzed oxidative C–C formation

4. Green chemistry: The development of cross-dehydrogenative coupling (CDC) for chemical synthesis

5. Cross-Dehydrogenative Coupling (CDC): Exploring C−C Bond Formations beyond Functional Group Transformations

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