Facile Synthesis of Diverse o-Iodoaryl Triflates from o-Silylaryl Triflates by Aluminum-mediated Desilyliodination-Reference-Cited by-同舟云学术

Facile Synthesis of Diverse o-Iodoaryl Triflates from o-Silylaryl Triflates by Aluminum-mediated Desilyliodination

Published:2019-07-05 Issue:7 Volume:48 Page:742-745
ISSN:0366-7022
Container-title:Chemistry Letters
language:en
Short-container-title:Chem. Lett.

Author:

Yoshida Suguru¹,Hazama Yuki¹,Kanemoto Kazuya¹,Nakamura Yu¹,Hosoya Takamitsu¹

Affiliation:

1. 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

Publisher

The Chemical Society of Japan

Subject

General Chemistry

Link

http://www.journal.csj.jp/doi/pdf/10.1246/cl.190223

Reference63 articles.

1. Recent advances in transition-metal-free carbon–carbon and carbon–heteroatom bond-forming reactions using arynes

2. The Renaissance and Bright Future of Synthetic Aryne Chemistry

3. Controlled Reactive Intermediates Enabling Facile Molecular Conjugation

4. Recent advances in reactions between arynes and organosulfur compounds

5. New efficient protocol for aryne generation. Selective synthesis of differentially protected 1,4,5-naphthalenetriols

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