@article{052dfb395fca44f3bb9e6cae4d4e5d21,
title = "Facile synthesis of 9,10,19,20-tetraalkylporphycenes",
abstract = "meso-Tetraalkylporphycenes were synthesized in a few steps using intramolecular oxidative coupling of the Z-isomer of 5,6-dialkyldipyrroethenes. The use of a hypervalent iodine(III) reagent, namely phenyliodine(III) bis(trifluoroacetate), is essential for performing these reactions.",
author = "Toshikazu Ono and Daiki Koga and Yoshio Hisaeda",
note = "Funding Information: This work was supported by the Precursory Research for Embryonic Science and Technology (PRESTO) Program {"}Hyper-nano-space Design toward Innovative Functionality{"} of the Japan Science and Technology Agency (JST). It was also supported by JSPS KAKENHI Grant Numbers JP16H04119 (Grant-in-Aid for Scientific Research (B) for Y. H.), JP16H01035 (Precisely Designed Catalysts with Customized Scaffolding for Y. H.), and JP15H00757 (Element Blocks for T. O.). We thank Dr. Kenji Yoza (Bruker AXS) for performing X-ray crystallographic analyses. Publisher Copyright: {\textcopyright} 2017 The Chemical Society of Japan.",
year = "2017",
doi = "10.1246/cl.161019",
language = "English",
volume = "46",
pages = "260--262",
journal = "Chemistry Letters",
issn = "0366-7022",
publisher = "The Chemical Society of Japan",
number = "2",
}