Facile synthesis of 9,10,19,20-tetraalkylporphycenes

Toshikazu Ono, Daiki Koga, Yoshio Hisaeda

Research output: Contribution to journal › Article

8 Citations (Scopus)

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.

Original languageEnglish
Pages (from-to)260-262
Number of pages3
JournalChemistry Letters
Volume46
Issue number2
DOIs
Publication statusPublished - Jan 1 2017

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Iodine
Isomers
phenyliodine(III) bis(trifluoroacetate)

All Science Journal Classification (ASJC) codes

  • Chemistry(all)

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Facile synthesis of 9,10,19,20-tetraalkylporphycenes. / Ono, Toshikazu; Koga, Daiki; Hisaeda, Yoshio.

In: Chemistry Letters, Vol. 46, No. 2, 01.01.2017, p. 260-262.

Research output: Contribution to journal › Article

Ono, T, Koga, D & Hisaeda, Y 2017, 'Facile synthesis of 9,10,19,20-tetraalkylporphycenes', Chemistry Letters, vol. 46, no. 2, pp. 260-262. https://doi.org/10.1246/cl.161019
Ono T, Koga D, Hisaeda Y. Facile synthesis of 9,10,19,20-tetraalkylporphycenes. Chemistry Letters. 2017 Jan 1;46(2):260-262. https://doi.org/10.1246/cl.161019
Ono, Toshikazu ; Koga, Daiki ; Hisaeda, Yoshio. / Facile synthesis of 9,10,19,20-tetraalkylporphycenes. In: Chemistry Letters. 2017 ; Vol. 46, No. 2. pp. 260-262.
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