Abstract
Combining palladium catalyzed reactions in one-pot reactions represents an efficient and
economical use of catalyst. The Suzuki-Miyaura cross-coupling has been proven to be a reaction
which can be combined with other palladium catalyzed reactions in the same pot. This mini-review
will highlight some of the latest examples where Suzuki-Miyaura cross-coupling reactions have been
combined with other palladium catalyzed reactions in one-pot reaction. Predominantly, examples
with homogeneous reaction conditions will be discussed in addition to a few examples from the authors
where Pd/C have been used as a catalyst.
Keywords:
Natural product synthesis, natural product synthesis, one-pot reaction, palladium catalyzed reaction, reductive amination,
suzuki-miyaura cross-coupling.
Graphical Abstract
[11]
Sydnes, M.O. Recent developments in the use of palladium on solid support in organic synthesis. Curr. Org. Synth., 2011, 8, 881-891.
[13]
Hung, T.Q.; Dang, T.T.; Pham, N.N.; Langer, P. Synthesis of fused
aromatic N-heterocycles by domino site-selective palladiumcatalyzed
C-C and C-N coupling reactions. In: Targets in Heterocyclic
Systems Chemistry and Properties; Attanasi, O. A.; Merino, P.; Spinelli, D., Eds.; Societá Chimica Italiana: Roma, 2017; 21, pp. 389-401.
[49]
Sydnes, M.O. Methods for converting nitro aryls to secondary aryl amines in one-pot. In: Advances in Chemistry Research; Taylor, J.C., Ed.; Nova Science Publishers, Inc.: New York, 2015; 25, pp. 58-77.
[56]
Vaaland, I.C. Naphthalene trans-dihydrodiols., Master thesis. University
of Stavanger, Norway. 2015.