2-(1-Hydroxypropyn-2-yl)-1-vinylpyrroles: the first successful Favorsky ethynylation of pyrrolecarbaldehydes
2015 ◽
Vol 11
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pp. 228-232
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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.
Keyword(s):
1986 ◽
Vol 22
(4)
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pp. 393-396
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1972 ◽
Vol 30
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pp. 428-429
1986 ◽
Vol 44
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pp. 724-725
Keyword(s):
1992 ◽
Vol 50
(1)
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pp. 318-319
1999 ◽
Vol 09
(PR8)
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pp. Pr8-251-Pr8-258
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1999 ◽
Vol 09
(PR8)
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pp. Pr8-221-Pr8-228
2001 ◽
Vol 11
(PR3)
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pp. Pr3-301-Pr3-306
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1986 ◽
Vol 47
(C8)
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pp. C8-159-C8-162
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