ChemInform Abstract: Highly Enantioselective Insertion of Carbenoids into O—H Bonds of Phenols: An...
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2008 Phenol ethers Q 0270 Highly Enantioselective Insertion of Carbenoids into O—H Bonds of Phenols: An Efficient Approach to Chiral α-Aryloxycarboxylic Esters. — Enantioselective in- sertion of carbenoids into phenolic O—H bonds is achieved using a copper/chiral spiro bisoxazoline complex as catalyst. — (CHEN, C.; ZHU, S.-F.; LIU, B.; WANG, L.-X.; ZHOU*, Q.-L.; J. Am. Chem. Soc. 129 (2007) 42, 12616-12617; State Key Lab. Elem.-Org. Chem., Nankai Univ., Tianjin 300071, Peop. Rep. China; Eng.) — Nuesgen 09- 086
Transcript of ChemInform Abstract: Highly Enantioselective Insertion of Carbenoids into O—H Bonds of Phenols: An...
2008
Phenol ethersQ 0270 Highly Enantioselective Insertion of Carbenoids into O—H Bonds of Phenols: An
Efficient Approach to Chiral α-Aryloxycarboxylic Esters. — Enantioselective in-sertion of carbenoids into phenolic O—H bonds is achieved using a copper/chiral spiro bisoxazoline complex as catalyst. — (CHEN, C.; ZHU, S.-F.; LIU, B.; WANG, L.-X.; ZHOU*, Q.-L.; J. Am. Chem. Soc. 129 (2007) 42, 12616-12617; State Key Lab. Elem.-Org. Chem., Nankai Univ., Tianjin 300071, Peop. Rep. China; Eng.) — Nuesgen
09- 086
