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

Toshikazu Ono; Daiki Koga; Yoshio Hisaeda

doi:10.1246/cl.161019

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

Toshikazu Ono
, Daiki Koga
, Yoshio Hisaeda

Applied Chemistry

Research output: Contribution to journal › Article › peer-review

25 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 language	English
Pages (from-to)	260-262
Number of pages	3
Journal	Chemistry Letters
Volume	46
Issue number	2
DOIs	https://doi.org/10.1246/cl.161019
Publication status	Published - 2017

All Science Journal Classification (ASJC) codes

General Chemistry

Access to Document

10.1246/cl.161019

Cite this

@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 = "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 = "Oxford University Press",

number = "2",

}

TY - JOUR

T1 - Facile synthesis of 9,10,19,20-tetraalkylporphycenes

AU - Ono, Toshikazu

AU - Koga, Daiki

AU - Hisaeda, Yoshio

PY - 2017

Y1 - 2017

N2 - 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.

AB - 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.

UR - https://www.scopus.com/pages/publications/85011622746

UR - https://www.scopus.com/pages/publications/85011622746#tab=citedBy

U2 - 10.1246/cl.161019

DO - 10.1246/cl.161019

M3 - Article

AN - SCOPUS:85011622746

SN - 0366-7022

VL - 46

SP - 260

EP - 262

JO - Chemistry Letters

JF - Chemistry Letters

IS - 2

ER -

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

Abstract

All Science Journal Classification (ASJC) codes

Access to Document

Other files and links

Fingerprint

Cite this