Setembro 2013 vol. 1 num. 1 - Brazilian Meeting on Organic Synthesis 2011
Abstract - Open Access.
Selective coupling reaction between 2,6-diiodoanisoles and terminal alkynes catalyzed by palladium complex.
Frota, Carlise ; Rossini, Allan F. C. ; Gariani, Rogério A. ; Raminelli, Cristiano ;
Abstract:
The cross-coupling reaction between aryl halides and terminal alkynes catalyzed by palladium complexes and copper (I) salts can be considered an useful synthetic tool in the C(sp2)-C(sp) bond formation leading to disubstituted acetylenic compounds. Accordingly, in this work we present our preliminary results involving the selective coupling reaction between 2,6-diiodoanisoles and terminal alkynes catalyzed by palladium and copper, in order to produce disubstituted alkynes bearing a functionalized aromatic ring.
Abstract:
Palavras-chave: cross-coupling reaction, selective reaction, palladium catalysis,
Palavras-chave: ,
DOI: 10.5151/chempro-14bmos-R0057-1
Referências bibliográficas
- [1] 1 Chinchilla, R.; Nájera, C. Chem. Rev. 2007, 107, 874.
Como citar:
Frota, Carlise; Rossini, Allan F. C.; Gariani, Rogério A.; Raminelli, Cristiano; "Selective coupling reaction between 2,6-diiodoanisoles and terminal alkynes catalyzed by palladium complex.", p. 57 . In: In Blucher Chemistry Proceedings, São Paulo, v. 1, n. 1, Setembro.2013.
São Paulo: Blucher,
2013.
ISSN 2318-4043,
DOI 10.5151/chempro-14bmos-R0057-1
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