Boron Trifluoride-Mediated Domino Dehydration/Electrophilic Cyclization of Silylalkynols Leading to 2,3-Fused Tricyclic Benzofulvenes-Reference-Cited by-同舟云学术

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Boron Trifluoride-Mediated Domino Dehydration/Electrophilic Cyclization of Silylalkynols Leading to 2,3-Fused Tricyclic Benzofulvenes

Published:2024-02-22 Issue:8 Volume:26 Page:1652-1656
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Okitsu Takashi¹^ORCID,Yoshikawa Takeshi²^ORCID,Morohashi Mai³,Aoki Kokoro²,Yakura Takayuki¹^ORCID,Sakata Ken²^ORCID,Hatano Manabu³^ORCID

Affiliation:

1. Faculty of Pharmaceutical Sciences, University of Toyama, Sugitani, Toyama 930-0194, Japan

2. Faculty of Pharmaceutical Sciences, Toho University, Funabashi, Chiba 274-8510, Japan

3. Faculty of Pharmaceutical Sciences, Kobe Pharmaceutical University, Kobe 658-8558, Japan

Funder

Japan Society for the Promotion of Science

Publisher

American Chemical Society (ACS)

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.4c00123

Reference19 articles.

1. Peripherally Selective Cannabinoid 1 Receptor (CB1R) Agonists for the Treatment of Neuropathic Pain

2. Synthesis and Structure of Conjugated Molecules with the Benzofulvene Core

3. Expanding the Scope: Monopentafulvene and -Benzofulvene Complexes of Zirconium and Hafnium

4. Facile Construction of Benzofulvene Scaffold from Tetraaryl[3]cumulene Through Electrophilic Iodocyclization

5. Palladium-Catalyzed Benzofulvenation of o -Arylanilines through C−H Bond Activation by Using Two Diarylacetylenes as an Implicit Benzofulvene

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