Construction of aziridine, azetidine, indole and quinoline-like heterocycles via Pd-mediated C–H activation/annulation strategies-Reference-Cited by-同舟云学术

Construction of aziridine, azetidine, indole and quinoline-like heterocycles via Pd-mediated C–H activation/annulation strategies

Published:2022 Issue: Volume: Page:
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Qiu Mengyu¹²³⁴,Fu Xuegang¹²³⁴,Fu Peng¹²³⁴,Huang Jianhui¹²³⁴^ORCID

Affiliation:

1. School of Pharmaceutical Science and Technology, Tianjin University, 92 Weijin Road, Nankai District, Tianjin 300072, China

2. Tianjin Key Laboratory for Modern Drug Delivery & High-Efficiency, China

3. Tianjin University and Health-Biotech United Group Joint Laboratory of Innovative Drug Development and Translational Medicine, China

4. Collaborative Innovation Center of Chemical Science and Engineering (Tianjin), Tianjin 300072, China

Abstract

N-Heterocycles can be found in natural products and drug molecules and are indispensable components in the area of organic synthesis, medicinal chemistry and materials science.

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/2022/OB/D1OB02146J

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4. Alkaloids Used as Medicines: Structural Phytochemistry Meets Biodiversity—An Update and Forward Look

5. O.Chuzel and O.Riant , Sparteine as a chiral ligand for asymmetric catalysis , in Chiral Diazaligands for Asymmetric Synthesis , Springer , Berlin, Germany , 2005

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