2-(1-Hydroxypropyn-2-yl)-1-vinylpyrroles: the first successful Favorsky ethynylation of pyrrolecarbaldehydes.
Beilstein J Org Chem
; 11: 228-32, 2015.
Article
en En
| MEDLINE
| ID: mdl-25815074
1-Vinylpyrrole-2-carbaldehydes react with acetylene at atmospheric pressure in a NaOH/EtOH/DMSO system at 7-10 °C to afford 2-(1-hydroxypropyn-2-yl)-1-vinylpyrroles in 53-94% yield. Thus, the first base-mediated direct ethynylation of pyrrolecarbaldehydes with free acetylene under modified conditions of the Favorsky reaction has been implemented to pave an expedient route to important biomolecules containing a pyrrole ring.
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01-internacional
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MEDLINE
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En
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Beilstein J Org Chem
Año:
2015
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Article
Pais de publicación:
Alemania