Multisubstituted naphthalene synthesis from 4-hydroxy-2-pyrones through [4+2] cycloaddition with <i>o</i>-silylaryl triflates-Reference-Cited by-同舟云学术

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Multisubstituted naphthalene synthesis from 4-hydroxy-2-pyrones through [4+2] cycloaddition with o-silylaryl triflates

Published:2023 Issue:40 Volume:47 Page:18762-18768
ISSN:1144-0546
Container-title:New Journal of Chemistry
language:en
Short-container-title:New J. Chem.

Author:

Numata Koyo¹,Tabata Shinya¹,Kobayashi Akihiro¹²,Yoshida Suguru¹^ORCID

Affiliation:

1. Department of Biological Science and Technology, Faculty of Advanced Engineering, Tokyo University of Science, 6-3-1 Niijuku, Katsushika-ku, Tokyo 125-8585, Japan

2. Laboratory of Chemical Bioscience, Institute of Biomaterials and Bioengineering, Tokyo Medical and Dental University (TMDU), 2-3-10 Kanda-Surugadai, Chiyoda-ku, Tokyo 101-0062, Japan

Abstract

An efficient synthetic method for multisubstituted naphthalenes from 4-hydroxy-2-pyrones through cycloaddition with aryne intermediates is disclosed.

Funder

Japan Society for the Promotion of Science

Tokuyama Science Foundation

Inamori Foundation

Ube Foundation

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,General Chemistry,Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2023/NJ/D3NJ03831A

Reference57 articles.

1. Naphthalene, a versatile platform in medicinal chemistry: Sky-high perspective

2. Naphthalene diimides: perspectives and promise

3. Design, synthesis, biochemical and in silico characterization of novel naphthalene-thiourea conjugates as potential and selective inhibitors of alkaline phosphatase

4. Modern methods for the synthesis of substituted naphthalenes

5. Regioselective C−H Functionalization of Naphthalenes: Reactivity and Mechanistic Insights

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