Asymmetric Synthesis of Pyrrolidines via Oxetane Desymmetrization-Reference-Cited by-同舟云学术

Asymmetric Synthesis of Pyrrolidines via Oxetane Desymmetrization

Published:2022-03-24 Issue:12 Volume:24 Page:2359-2364
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Zhang Renwei¹²³,Sun Meng¹^ORCID,Yan Qiaolin¹,Lin Xingbang¹,Li Xin¹,Fang Xin¹,Sung Herman H. Y.¹,Williams Ian D.¹,Sun Jianwei¹²^ORCID

Affiliation:

1. Department of Chemistry and the Hong Kong Branch of Chinese National Engineering Research Centre for Tissue Restoration & Reconstruction, The Hong Kong University of Science and Technology (HKUST), Clear Water Bay, Kowloon, Hong Kong SAR, China

2. Shenzhen Research Institute, HKUST, No. 9 Yuexing 1st Road, Shenzhen 518057, China

3. Shenzhen Bay Laboratory, Shenzhen 518107, China

Funder

National Natural Science Foundation of China

Shenzhen Science and Technology Innovation Committee

Hong Kong Research Grants Council

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.2c00564

Reference64 articles.

1. Analysis of the Structural Diversity, Substitution Patterns, and Frequency of Nitrogen Heterocycles among U.S. FDA Approved Pharmaceuticals

2. Rings in Drugs

3. Pyrrolidinyl-Spirooxindole Natural Products as Inspirations for the Development of Potential Therapeutic Agents

4. Horsfiline, an oxindole alkaloid from Horsfieldia superba

5. Mesembrine: The archetypal psycho-active Sceletium alkaloid

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