Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5269564 | Tetrahedron Letters | 2011 | 5 Pages |
Abstract
Sonogashira cross-coupling reactions involving (E)-iodo vinyl stannanes and terminal acetylenes were carried out in the presence of Pd(PPh3)4, CuI and several amines, affording (Z)-tributylstannyl enynes in moderate to good yields (62-91%). Utilizing the catalytic system containing Pd(PPh3)4 (5%), CuI (10%), and TBAOH (40% in aqueous media) as activator, better yields (72-91%) and lower reaction times were achieved.
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Authors
Carlos E.D. Nazario, Amanda S. Santana, Cristiane Y. Kawasoko, Carlos A. Carollo, Gabriela R. Hurtado, Luiz H. Viana, Sandro L. Barbosa, Palimécio G. Jr., Francisco A. Marques, Vânia B. Dabdoub, Miguel J. Dabdoub, Adriano C.M. Baroni,