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Diastereoselective palladium-catalyzed functionalization of prochiral C(sp 3 )-H bonds of aliphatic and alicyclic compounds.

Srinivasarao Arulananda BabuYashika AggarwalPooja PatelRadha Tomar
Published in: Chemical communications (Cambridge, England) (2022)
We highlight the reported developments of the palladium-catalyzed C-H activation and functionalization of the inactive/unreactive prochiral C(sp 3 )-H bonds of aliphatic and alicyclic compounds. There exist numerous classical methods for generating contiguous stereogenic centers in a compound with a high degree of stereocontrol. Along similar lines, the Pd(II)-catalyzed, directing group-aided functionalization of inactive prochiral/diastereotopic C(sp 3 )-H bonds have been exploited to accomplish the stereoselective construction of stereo-arrays in organic compounds. We present a concise discussion on how specific strategies consisting of Pd(II)-catalyzed, directing group-aided C(sp 3 )-H functionalization have been utilized to generate two or more stereogenic centers in aliphatic and alicyclic compounds.
Keyphrases
  • room temperature
  • water soluble