Selective C–O Bond Forming Reactions at Indole-C2-Position toward Polycyclic Indolone or Indolinone Derivatives Tethered with Medium-Sized Rings-Reference-Cited by-同舟云学术

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Selective C–O Bond Forming Reactions at Indole-C2-Position toward Polycyclic Indolone or Indolinone Derivatives Tethered with Medium-Sized Rings

Published:2022-08-18 Issue:34 Volume:24 Page:6272-6276
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Wang Zongkang¹^ORCID,Yin Liqiang¹,Wang Mengdan¹^ORCID,Zhu Yilin¹,Yang Yajie¹^ORCID,Cheng Lu¹,Wang Chengyu²^ORCID,Li Yanzhong¹³^ORCID

Affiliation:

1. School of Chemistry and Molecular Engineering, East China Normal University, 500 Dongchuan Road, Shanghai, 200241, China

2. School of Chemistry and Chemical Engineering, Linyi University, Shuangling Road, Linyi, Shandong 276000, China

3. Key Laboratory of Polar Materials and Devices, Ministry of Education, East China Normal University, Shanghai 200062, China

Funder

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.2c02398

Reference28 articles.

1. A general strategy for diversifying complex natural products to polycyclic scaffolds with medium-sized rings

2. Synthesis and Functionalization of Indoles Through Palladium-catalyzed Reactions

3. Synthesis of Indole-Fused Six-, Seven-, or Eight-Membered N,O-Heterocycles via Rhodium-Catalyzed NH-Indole-Directed C–H Acetoxylation/Hydrolysis/Annulation

4. N-[(1-Butyl-4-piperidinyl)methyl]-3,4- dihydro-2H-[1,3]oxazino[3,2-a]indole- 10-carboxamide hydrochloride: the first potent and selective 5-HT4 receptor antagonist amide with oral activity.

5. Synthesis and pharmacological activity of metabolites of the 5-HT4 receptor antagonist SB-207266

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