Palladium-Catalyzed Regioselective C4-H Acyloxylation of Indoles with Carboxylic Acids via a Transient Directing Groups Strategy-Reference-Cited by-同舟云学术

Palladium-Catalyzed Regioselective C4-H Acyloxylation of Indoles with Carboxylic Acids via a Transient Directing Groups Strategy

Published:2023-12-27 Issue:1 Volume:26 Page:41-45
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Zhang Xing-Long¹²,Wang Meng-Yue²,Liu Hui-Jin¹,Wang Yong-Qiang²^ORCID

Affiliation:

1. Shaanxi Key Laboratory of Low Metamorphic Coal Clean Utilization, School of Chemistry and Chemical Engineering, Yulin University, Yulin 719000, Shaanxi, P.R. China

2. Key Laboratory of Synthetic and Natural Functional Molecule Chemistry of Ministry of Education, College of Chemistry & Materials Science, Northwest University, Xi’an 710069, P.R. China

Funder

Yulin Science and Technology Bureau

Scientific Research Plan Projects of Shaanxi Education Department

National Natural Science Foundation of China

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.3c03568

Reference35 articles.

1. Marine Indole Alkaloids: Potential New Drug Leads for the Control of Depression and Anxiety

2. Beyond C2 and C3: Transition-Metal-Catalyzed C–H Functionalization of Indole

3. Solid-phase synthesis of JBIR-126 (Tambromycin), JBIR-35 and their analogs

4. Total Synthesis of the Cyclic Peptide Argyrin B

5. Identification of opioid receptor subtypes in antinociceptive actions of supraspinally-admintstered mitragynine in mice

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