Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5273355 | Tetrahedron Letters | 2010 | 4 Pages |
Abstract
3-Iodo-4-chalcogen-2H-benzopyran derivatives underwent a direct Sonogashira cross-coupling reaction with several terminal alkynes in the presence of a catalytic amount of Pd(PPh3)2Cl2 with CuI as a co-catalyst, using Et3N as base and solvent. This cross-coupling reaction proceeded cleanly under mild conditions and was performed with propargylic alcohols, propargylic ethers, as well as alkyl and aryl alkynes, furnishing the correspondent 3-alkynyl-4-chalcogen-2H-benzopyrans in good yields.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Adriane Sperança, Benhur Godoi, Ana C.G. Souza, Gilson Zeni,