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Selective Synthesis of Tripyrranes, Tetrapyrranes, and Corroles
Author(s) -
Aydin Gokcen,
Temelli Baris,
Unaleroglu Canan
Publication year - 2015
Publication title -
european journal of organic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.825
H-Index - 155
eISSN - 1099-0690
pISSN - 1434-193X
DOI - 10.1002/ejoc.201501062
Subject(s) - chemistry , pyrrole , combinatorial chemistry , catalysis , reaction conditions , organic chemistry
A new, catalytic, and general methodology was developed for the direct synthesis of unsymmetrical AB‐type tripyrranes by reaction of dipyrromethanesulfonamides with pyrrole. Key structure dipyrromethanesulfonamides were synthesized by the addition of meso ‐substituted dipyrromethanes to Cu(OTf) 2 ‐activated tosylimines. The introduced method enables selective preparation of tetrapyrranes in high yields by tuning the conditions of the addition reaction. The oxidation of tetrapyrranes by 2,3‐dichloro‐5,6‐dicyano‐1,4‐benzoquinone afforded only corresponding A 3 ‐ and trans ‐A 2 B‐corroles.