Cation-directed enantioselective N-functionalization of pyrroles
A catalytic enantioselective N-functionalization of pyrroles has been developed. Imines formed in situ via condensation underwent cation-directed cyclization with complete N-regioselectivity. The cyclized products were obtained with enantiomeric ratios up to 96:4 for aldimine substrates and up to 99...
| Main Authors: | , , |
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| Format: | Journal article |
| Published: |
Thieme Publishing
2016
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