Abstract
Even though halogen bonding – the noncovalent interaction between
electrophilic halogen substituents and Lewis bases – has now been established
in molecular recognition and catalysis, its use in enantioselective processes
is still very little explored. Herein, we present the synthesis of chiral
bidentate halogen bond donors based on two iodoimidazolium units with rigidly
attached chiral sidearms. With these Lewis acids, chiral recognition of a
racemic diamine is achieved in NMR studies. DFT calculations support a 1:1
interaction of the halogen bond donor with both enantiomers and indicate that
the chiral recognition is based on a different spatial orientation of the Lewis
bases in the halogen bonded complexes. In addition, moderate enantioselectivity
is achieved in a Mukaiyama aldol reaction with a preorganized variant of the chiral
halogen bond donor. This represents the first case in which asymmetric
induction was realized with a pure halogen bond donor lacking any additionally
active functional groups.
Supplementary materials
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