Synthesis of Chiral Spirolactams via Sequential C−H Olefination/Asymmetric [4+1] Spirocyclization under a Simple Co II /Chiral Spiro Phosphoric Acid Binary System-Reference-Cited by-同舟云学术

Synthesis of Chiral Spirolactams via Sequential C−H Olefination/Asymmetric [4+1] Spirocyclization under a Simple Co II /Chiral Spiro Phosphoric Acid Binary System

Published:2021-09-24 Issue:43 Volume:133 Page:23371-23376
ISSN:0044-8249
Container-title:Angewandte Chemie
language:en
Short-container-title:Angew. Chem.

Author:

Yuan Wen‐Kui¹,Shi Bing‐Feng¹²³^ORCID

Affiliation:

1. Center of Chemistry for Frontier Technologies Department of Chemistry Zhejiang University Hangzhou 310027 China

2. College of Chemistry and Molecular Engineering Zhengzhou University Zhengzhou 450001 China

3. School of Chemistry and Chemical Engineering Henan Normal University Xinxiang 453007 China

Funder

National Natural Science Foundation of China

Postdoctoral Research Foundation of China

Publisher

Wiley

Subject

General Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ange.202108853

Reference134 articles.

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3. Novel spirosuccinimides with incorporated isoindolone and benzisothiazole 1,1-dioxide moieties as aldose reductase inhibitors and antihyperglycemic agents

4. Spirostaphylotrichin X from a Marine-Derived Fungus as an Anti-influenza Agent Targeting RNA Polymerase PB2

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