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One‐Step Synthesis of [16]Helicene
Author(s) -
Mori Kazuyuki,
Murase Takashi,
Fujita Makoto
Publication year - 2015
Publication title -
angewandte chemie international edition
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.831
H-Index - 550
eISSN - 1521-3773
pISSN - 1433-7851
DOI - 10.1002/anie.201502436
Subject(s) - helicene , chemistry , organic chemistry , molecule
A single‐strand arylene–vinylene precursor containing four phenylene and three naphthylene units linked together with six vinylene spacers undergoes helical folding via sextuple photocyclization to give a [16]helicene core in a single step. The phenylene and naphthylene units are arranged in the precursor such that unfavorable side reactions (anthracene or benzoperylene formation) are avoided, and this is the key to the success of the one‐step synthesis of [16]helicene, which is the longest [ n ]helicene that has been synthesized to date.