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Effective synthesis of diiodinated picene and dibenzo[a,h]anthracene by AuCl-catalyzed double cyclization

6,13-Diiododibenzo[a,h]anthracene and 5,8-diiodopicene were synthesized by AuCl-catalyzed double cyclization. The highly selective reaction yielded a new class of peri-halogenated fused aromatics.

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Published in:Tetrahedron letters 2012-03, Vol.53 (13), p.1617-1619
Main Authors: Nakae, Takahiro, Ohnishi, Ryuji, Kitahata, Yoshiharu, Soukawa, Tatsuya, Sato, Hisako, Mori, Shigeki, Okujima, Tetsuo, Uno, Hidemitsu, Sakaguchi, Hiroshi
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cited_by cdi_FETCH-LOGICAL-c405t-c08f5af5a8b4ec73cf3b02e7134dc51188743cfe077a95d89493a9391417f1013
cites cdi_FETCH-LOGICAL-c405t-c08f5af5a8b4ec73cf3b02e7134dc51188743cfe077a95d89493a9391417f1013
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container_issue 13
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container_title Tetrahedron letters
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creator Nakae, Takahiro
Ohnishi, Ryuji
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Sakaguchi, Hiroshi
description 6,13-Diiododibenzo[a,h]anthracene and 5,8-diiodopicene were synthesized by AuCl-catalyzed double cyclization. The highly selective reaction yielded a new class of peri-halogenated fused aromatics.
doi_str_mv 10.1016/j.tetlet.2012.01.071
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source ScienceDirect Freedom Collection
subjects Cyclization
Fused-ring system
Gold catalysis
Polyaromatics
Rearrangement
Synthesis (chemistry)
Tetrahedrons
title Effective synthesis of diiodinated picene and dibenzo[a,h]anthracene by AuCl-catalyzed double cyclization
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