Access to thiionized-, selenolized-, and alkylated 5-alkylidene 3-pyrrolin-2-one derivatives <i>via</i> a regioselective oxidative annulation reaction-Reference-Cited by-同舟云学术

Access to thiionized-, selenolized-, and alkylated 5-alkylidene 3-pyrrolin-2-one derivatives via a regioselective oxidative annulation reaction

Published:2023 Issue:12 Volume:21 Page:2596-2602
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Liu Donghan¹,Song Siyu¹,Chen Longkun¹,Zhang Mingshuai¹,Liu Zhuoyuan¹,Lu Xihang¹,Huang Jiuzhong²^ORCID,Yu Fuchao¹^ORCID

Affiliation:

1. Faculty of Life Science and Technology, Kunming University of Science and Technology, Kunming, 650500, P. R. China

2. School of Pharmacy and Key Laboratory of Prevention and Treatment of Cardiovascular and Cerebrovascular Diseases of Ministry of Education, Gannan Medical University, Ganzhou, 341000, P. R. China

Abstract

Polyfunctional thiionized-, selenolized-, and alkylated 5-alkylidene 3-pyrrolin-2-one derivatives are easily constructed via a metal-free regioselective oxidative annulation reaction.

Funder

National Natural Science Foundation of China

Natural Science Foundation of Yunnan Province

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2023/OB/D3OB00014A

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1. Dietary phenolics: chemistry, bioavailability and effects on health

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4. Nickel-promoted oxidative domino Csp3–H/N–H bond double-isocyanide insertion reaction to construct pyrrolin-2-ones

5. Development of Methods for the Synthesis of Libraries of Substituted Maleimides and α,β-Unsaturated-γ-butyrolactams

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