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  • Pd-PEPPSI-IPent: an active, sterically demanding cross-coupling catalyst and its application in the synthesis of tetra-ortho-substituted biaryls.

Pd-PEPPSI-IPent: an active, sterically demanding cross-coupling catalyst and its application in the synthesis of tetra-ortho-substituted biaryls.

Angewandte Chemie (International ed. in English) (2009-02-20)
Michael G Organ, Selçuk Calimsiz, Mahmoud Sayah, Ka Hou Hoi, Alan J Lough
ABSTRACT

Incredible Bulk: A series of N-heterocyclic carbene catalysts (see picture) were prepared and evaluated in the Suzuki-Miyaura reaction. A variety of sterically encumbered tetra-ortho-substituted biaryl products were formed from unreactive aryl chlorides using the isopentyl-substituted catalyst at temperatures ranging from 65 degrees C to room temperature. The cyclopentyl-substituted catalyst was virtually inactive, demonstrating that "flexible bulk" is essential to promote these transformations.

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Sigma-Aldrich
Pd-PEPPSI-IPent catalyst, ≥95%
Sigma-Aldrich
1,3-Bis(2,6-di(3-pentyl)phenyl)imidazolium chloride, ≥95%