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  • Copper-catalyzed Petasis-type reaction: a general route to α-substituted amides from imines, acid chlorides, and organoboron reagents.

Copper-catalyzed Petasis-type reaction: a general route to α-substituted amides from imines, acid chlorides, and organoboron reagents.

The Journal of organic chemistry (2012-01-31)
Marie S T Morin, Yingdong Lu, Daniel A Black, Bruce A Arndtsen
ZUSAMMENFASSUNG

A copper-catalyzed Petasis-type reaction of imines, acid chlorides, and organoboranes to form α-substituted amides is described. This reaction does not require the use of activated imines or the transfer of special units from the organoboranes and represent a useful generalization of the Petasis reaction.

MATERIALIEN
Produktnummer
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Produktbeschreibung

Sigma-Aldrich
Kupfer(I)-chlorid, ReagentPlus®, purified, ≥99%
Sigma-Aldrich
p-Toluinsäure, 98%
Sigma-Aldrich
Kupfer(I)-chlorid, ≥99.995% trace metals basis
Sigma-Aldrich
Kupfer(I)-chlorid, AnhydroBeads, ≥99.99% trace metals basis