Abstract
Axially chiral biaryls and N-aryl indoles are stereoselectively prepared by utilizing planar chiral transition metal complexes. Both enantiomers of axial biaryls and N-aryl indoles could be synthesized starting from an identical enantiomerically pure arene chromium complex. We applied this method to the synthesis of vancomycin A-B ring system and korupensamines. Kinetically controlled biaryl and N-aryl indole transition metal complexes with sp 3 heteroatom at the side chain could be converted to thermodynamically stable complexes involving the inversion or transfer of planar chirality. These results indicate that transition metal fragment in planar chiral η-transition metal complexes can be utilized as dynamic complexes with mobile chiral auxiliary.
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Kamikawa, K. (2008). Asymmetric synthesis of axially chiral compound utilizing planar chiral transition metal complexes and their development for dynamic complexes. Yuki Gosei Kagaku Kyokaishi/Journal of Synthetic Organic Chemistry. Society of Synthetic Organic Chemistry. https://doi.org/10.5059/yukigoseikyokaishi.66.953
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