P(NMe2)3-Mediated Reductive Intramolecular Annulation of Benzoylformates Tethered with a Trisubstituted Alkene Unit and Synthesis of 2,2-Disubstituted 2H-Chromenes-Reference-Cited by-同舟云学术

P(NMe2)3-Mediated Reductive Intramolecular Annulation of Benzoylformates Tethered with a Trisubstituted Alkene Unit and Synthesis of 2,2-Disubstituted 2H-Chromenes

Published:2021-02-17 Issue:5 Volume:23 Page:1880-1885
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Zhang Jiayong¹,Qiu Yuhe¹,Zhang Biao¹,Huang Zhiqiang¹,He Zhengjie¹²^ORCID

Affiliation:

1. The State Key Laboratory of Elemento-Organic Chemistry, College of Chemistry, Nankai University, Tianjin 300071, China

2. Collaborative Innovation Center of Chemical Science and Engineering (Tianjin), Tianjin 300071, China

Funder

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.1c00286

Reference59 articles.

1. Natural Product-like Combinatorial Libraries Based on Privileged Structures. 1. General Principles and Solid-Phase Synthesis of Benzopyrans

2. Selenium-Based Solid-Phase Synthesis of Benzopyrans I: Applications to Combinatorial Synthesis of Natural Products

3. Tuberatolides, Potent FXR Antagonists from the Korean Marine Tunicate Botryllus tuberatus

4. Natural and Synthetic Chromenes, Fused Chromenes, and Versatility of Dihydrobenzo[h]chromenes in Organic Synthesis

5. Two carbazole alkaloids from Murraya koenigii

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