Pd(II)-Catalyzed Intramolecular C(sp2)–H Arylation of Tryptamines Using the Nonsteric NH2 as a Directing Group-Reference-Cited by-同舟云学术

Pd(II)-Catalyzed Intramolecular C(sp2)–H Arylation of Tryptamines Using the Nonsteric NH2 as a Directing Group

Published:2020-12-17 Issue:1 Volume:23 Page:42-48
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Wang Sixi¹,Yu Bin¹^ORCID,Liu Hong-Min¹^ORCID

Affiliation:

1. School of Pharmaceutical Sciences & Key Laboratory of Advanced Drug Preparation Technologies, Ministry of Education, Zhengzhou University, Zhengzhou 450001, China

Funder

China Postdoctoral Science Foundation

National Natural Science Foundation of China

Program for Science & Technology Innovation Talents in Universities of Henan Province

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.0c03668

Reference67 articles.

1. Total synthesis of the dictyodendrins as an arena to highlight emerging synthetic technologies

2. Variolins and Related Alkaloids

3. Osimertinib (AZD9291)—a science-driven, collaborative approach to rapid drug design and development

4. 2-Substituted Tryptamines: Agents with Selectivity for 5-HT6 Serotonin Receptors

5. Overlapping, Nonidentical Binding Sites of Different Classes of Nonpeptide Antagonists for the Human Gonadotropin-Releasing Hormone Receptor

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