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Menthane‐Based Chloride‐Bridged η 3 ‐Bis‐π‐Allylpalladium Chloride Dimers: Catalytic Asymmetric Allylation of Imines
Author(s) -
Jha Amit K.,
Fernandes Rodney A.
Publication year - 2019
Publication title -
european journal of organic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.825
H-Index - 155
eISSN - 1099-0690
pISSN - 1434-193X
DOI - 10.1002/ejoc.201900177
Subject(s) - chemistry , dimer , chloride , catalysis , medicinal chemistry , organic chemistry , stereochemistry
Menthane‐based η 3 ‐bis‐π‐allylpalladium chloride dimer complexes have been prepared for the first time. They exist as dimeric η 3 ‐bis‐π‐allylpalladium with four chloride bridges. The complexes catalyze the asymmetric allylation of various imines with allyltributylstannane and one equivalent of water to give chiral homoallylamines in yields of 60–77 % and enantioselectivity up to er = 93:7. The stereochemical information from the menthane framework was translated successfully through the η 3 ‐bis‐ π ‐allylpalladium catalysts in asymmetric allylation of imines.