Diastereoselective Synthesis of 1,2-Dihydrobenzofuro[3,2-b]pyridines via a Carbon–Carbon Double-Bond Cleavage/Rearrangement Cascade-Reference-Cited by-同舟云学术

Diastereoselective Synthesis of 1,2-Dihydrobenzofuro[3,2-b]pyridines via a Carbon–Carbon Double-Bond Cleavage/Rearrangement Cascade

Published:2021-03-17 Issue:7 Volume:23 Page:2654-2658
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Zhu Chi-Fan¹,Chen Ling-Qi¹,Hao Wen-Juan¹,Cui Chen-Chang¹,Tu Shu-Jiang¹^ORCID,Jiang Bo¹^ORCID

Affiliation:

1. School of Chemistry & Materials Science, Jiangsu Key Laboratory of Green Synthetic Chemistry for Functional Materials, Jiangsu Normal University, Xuzhou 221116, P. R. 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.1c00564

Reference41 articles.

1. New alkaloids from the fruiting bodies of Ganoderma sinense

2. Synthesis and biological evaluation of novel angularly fused polycyclic coumarins

3. Synthesis and Antitumor Properties of N-[2-(Dimethylamino)ethyl]carboxamide Derivatives of Fused Tetracyclic Quinolines and Quinoxalines: A New Class of Putative Topoisomerase Inhibitors

4. Optimization of novel benzofuro[3,2-b]pyridin-2(1H)-one derivatives as dual inhibitors of BTK and PI3Kδ

5. Design and synthesis of benzofuro[3,2-b]pyridin-2(1H)-one derivatives as anti-leukemia agents by inhibiting Btk and PI3Kδ

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