One-Step Synthesis of Hydropyrrolo[3,2-<i>b</i>]indoles via Cascade Reactions of Oxindole-Derived Nitrones with Allenoates-Reference-Cited by-同舟云学术

One-Step Synthesis of Hydropyrrolo[3,2-b]indoles via Cascade Reactions of Oxindole-Derived Nitrones with Allenoates

Published:2022-11-10 Issue:46 Volume:24 Page:8493-8497
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Luo Meng-Lan¹,Hou Qiumeng¹,Liu Shuai-Jiang¹,Zhao Qian¹,Qin Rui¹,Peng Cheng¹^ORCID,Han Bo¹^ORCID,Zhan Gu¹^ORCID

Affiliation:

1. State Key Laboratory of Southwestern Chinese Medicine Resources, School of Pharmacy, Chengdu University of Traditional Chinese Medicine, Chengdu 611137, P. R. China

Funder

China Postdoctoral Science Foundation

Chengdu University of Traditional Chinese Medicine

Department of Science and Technology of Sichuan Province

National Health Commission of the People's Republic of China

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.2c03349

Reference49 articles.

1. Chemistry of the Hexahydropyrrolo[2,3-b]indoles: Configuration, Conformation, Reactivity, and Applications in Synthesis

2. Structure, Bioactivity and Synthesis of Natural Products with Hexahydropyrrolo[2,3-b]indole

3. Recent Developments in the Catalytic, Asymmetric Construction of Pyrroloindolines Bearing All-Carbon Quaternary Stereocenters

4. Catalytic asymmetric preparation of pyrroloindolines: strategies and applications to total synthesis

5. Biosynthesis of pyrroloindoline-containing natural products

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