Journal
CHEMICAL COMMUNICATIONS
Volume -, Issue 41, Pages 6198-6200Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/b912108k
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Funding
- National Natural Science Foundation of China [20732005]
- State Basic Research and Development Program [2006CB806105]
- Chinese Academy of Sciences
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In this paper, we developed a new bisoxazoline ligand with a spiro skeleton and a alpha-naphthylmethyl substituent, i.e. (R-a,S,S)-L3, which has been successfully applied to the highly enantioselective cyclic allylation based on the carbopalladation of 3,4-allenyl hydrazines with ee values ranging from 92-95%.
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