Asymmetric Tandem Michael Addition/Interrupted Nef Reactions of Nitromethane with Oxindole-Derived Alkenes: Enantioselective Synthesis of Spiro-polycyclic Oxindoles-Reference-Cited by-同舟云学术

Asymmetric Tandem Michael Addition/Interrupted Nef Reactions of Nitromethane with Oxindole-Derived Alkenes: Enantioselective Synthesis of Spiro-polycyclic Oxindoles

Published:2024-04-05 Issue:15 Volume:26 Page:3279-3283
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Liu Shengshu¹,Yang Yu-Chen¹,Yang Yong-Qi¹,Li Xin¹,Wang Pengfei¹^ORCID,Li Yin-Long²^ORCID,Deng Jun¹^ORCID

Affiliation:

1. Chongqing Key Laboratory of Natural Product Synthesis and Drug Research, School of Pharmaceutical Sciences, Chongqing University, Chongqing 401331, China

2. Department of Radiology and Imaging Sciences, Emory University, 1364 Clifton Rd, Atlanta 30322, Georgia, United States

Funder

Chongqing Municipal Science and Technology Bureau

National Natural Science Foundation of China

Shaanxi Provincial Science and Technology Department

Publisher

American Chemical Society (ACS)

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.4c00919

Reference38 articles.

1. Spirooxindoles: Promising scaffolds for anticancer agents

2. An overview of spirooxindole as a promising scaffold for novel drug discovery

3. Two New Types of Bisindole Alkaloid from Trigonostemon lutescens

4. Isolation and characterization of new lactam compounds that inhibit lung and colon cancer cells from adlay (Coix lachryma-jobi L. var. ma-yuen Stapf) bran

5. Antiproliferative Lactams and Spiroenone from Adlay Bran in Human Breast Cancer Cell Lines

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