Abstract
The heterofunctionalisation of C-H, C=C and C≡C bonds is an important type of transformation that converts readily accessible precursors to valuable intermediates in organic synthesis, particularly when the heteroatom = N or O. The progress in this area of homogeneous catalysis by palladium is described in the current review, covering the period between 2005-early 2010. Asymmetric reactions remain a key challenge in this area, which is highlighted.
Keywords: Palladium, homogeneous catalysis, C-H activation, C-C bond formation, C-X bond formation, catalytic cycles, Hydroamination, allylic electrophiles, Oxidative Amination Reactions, cyclooctadiene (COD), Diamination of Alkenes, Bronsted basic DIPEA, diastereoselectivity, Dioxygenation, Aminoacetoxylation, Diamination of, hydroquinone (HQ), chiral palladium(, aza-Michael reactions
Call for Papers in Thematic Issues
Catalytic C-H bond activation as a tool for functionalization of heterocycles
The major topic is the functionalization of heterocycles through catalyzed C-H bond activation. The strategies based on C-H activation not only provide straightforward formation of C-C or C-X bonds but, more importantly, allow for the avoidance of pre-functionalization of one or two of the cross-coupling partners. The beneficial impact of ...read more
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