Synthesis of Benzofused Dioxabicycle Scaffolds via a Catellani Strategy-Reference-Cited by-同舟云学术

Synthesis of Benzofused Dioxabicycle Scaffolds via a Catellani Strategy

Published:2019-10-31 Issue:22 Volume:21 Page:8938-8942
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Wu Chenggui¹,Yang Xinjun¹,Shang Yong¹,Cheng Hong-Gang¹,Yan Wei¹,Zhou Qianghui¹²^ORCID

Affiliation:

1. Sauvage Center for Molecular Sciences, Engineering Research Center of Organosilicon Compounds & Materials (Ministry of Education), College of Chemistry and Molecular Sciences, Wuhan University, 430072 Wuhan, China

2. Institute for Advanced Studies, Wuhan University, 430072 Wuhan, China

Funder

China Postdoctoral Science Foundation

Wuhan University

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.9b03228

Reference63 articles.

1. Carbazole Alkaloids from the Stems of Clausena lansium

2. Short, Efficient Syntheses of the Amaryllidaceae Alkaloids (-)-Amabiline and (-)-Augustamine via Intramolecular 2-Azaallyl Anion Cycloadditions

3. Diterpenoids from Vellozia declinans

4. Integrastatins: structure and HIV-1 integrase inhibitory activities of two novel racemic tetracyclic aromatic heterocycles produced by two fungal species

5. One-Pot Construction of Aza- or Oxa-Bridged Benzocycloheptanes from Readily Available 2,3-Allenyl Malonates or 2,3-Allenols ando-Iodobenzaldehyde or Imine

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