Preparation of dipyrrins from F-BODIPYs by treatment with methanesulfonic acids | Zendy

J. Urieta | Zendy; Beatriz Lora Maroto | Zendy; Florencio Moreno | Zendy; Antonia R. Agarrabeitia | Zendy; María J. Ortiz | Zendy; Santiago de la Moya Cerero | Zendy

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Preparation of dipyrrins from F-BODIPYs by treatment with methanesulfonic acids

Author(s) -

J. Urieta,

Beatriz Lora Maroto,

Florencio Moreno,

Antonia R. Agarrabeitia,

María J. Ortiz,

Santiago de la Moya Cerero

Publication year - 2015

Publication title -

rsc advances

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 0.746

H-Index - 148

ISSN - 2046-2069

DOI - 10.1039/c5ra14914b

Subject(s) - methanesulfonic acid , chemistry , combinatorial chemistry , organic chemistry

An alternative metal-free soft procedure for the preparation of dipyrrins from F-BODIPYs is reported. The new method makes possible to obtain certain dipyrrin derivatives that were unaccessible from F-BODIPYs to date. To demonstrate the ability of the new procedure, dipyrrins having highly reactive groups, such as chloro, cyano or acetoxyl, have been easily obtained from the corresponding F-BODIPY, which shows the synthetic utility of the reported methodology

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