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• W2065877006 abstract "Easily obtained in a single step from bipyrrolic precursors in yields over 70 %, cyclo[8]pyrroles represent a new class of porphyrin analogues that display the classic disklike structure of porphyrins. The X-ray crystal structure of one of the cyclo[8]pyrroles obtained (see picture) shows that the macrocycle acts as a formal diprotonated receptor and forms eight hydrogen bonds to a sulfate ion bound within its core." @default.
• W2065877006 created "2016-06-24" @default.
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• W2065877006 date "2002-04-15" @default.
• W2065877006 modified "2023-10-10" @default.
• W2065877006 title "Cyclo[8]pyrrole: A Simple-to-Make Expanded Porphyrin with No Meso Bridges" @default.
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• W2065877006 doi "https://doi.org/10.1002/1521-3773(20020415)41:8<1422::aid-anie1422>3.0.co;2-o" @default.
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