Synthesis of 2-Iodoazulenes by the Iododeboronation of Azulen-2-ylboronic Acid Pinacol Esters with Copper(I) Iodide-Reference-Cited by-同舟云学术

Synthesis of 2-Iodoazulenes by the Iododeboronation of Azulen-2-ylboronic Acid Pinacol Esters with Copper(I) Iodide

Published:2018-01-19 Issue:3 Volume:83 Page:1298-1303
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Narita Masahiro¹,Murafuji Toshihiro¹²³^ORCID,Yamashita Saki²,Fujinaga Masayuki³,Hiyama Kumiko³,Oka Yurie³,Tani Fumito⁴,Kamijo Shin¹²^ORCID,Ishiguro Katsuya¹²

Affiliation:

1. Graduate School of Sciences and Technology for Innovation, Yamaguchi University, Yamaguchi 753-8512, Japan

2. Department of Chemistry, Faculty of Science, Yamaguchi University, Yamaguchi 753-8512, Japan

3. Graduate School of Medicine, Yamaguchi University, Yamaguchi 753-8512, Japan

4. Institute for Materials Chemistry and Engineering, Kyushu University, Fukuoka 819-0395, Japan

Funder

Japan Society for the Promotion of Science

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.7b02820

Reference76 articles.

1. Application of Azulene in Constructing Organic Optoelectronic Materials: New Tricks for an Old Dog

2. Azulene-based organic functional molecules for optoelectronics

3. Selective Dual-Channel Imaging on Cyanostyryl-Modified Azulene Systems with Unimolecularly Tunable Visible-Near Infrared Luminescence

4. 2,5-Bis(azulenyl)pyrrolo[3,2-b]pyrroles – the key influence of the linkage position on the linear and nonlinear optical properties

5. An Azulene‐Fused Tetracene Diimide with a Small HOMO–LUMO Gap

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