Catalytic enantioselective deprotonation of meso-epoxides utilising homochiral bis-lithium amide bases
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Tierney, JP
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UNIV PARIS 06,URA 473 CNRS,LAB CHIM ORGANOELEMENTS,F-75252 PARIS 05,FRANCEUNIV PARIS 06,URA 473 CNRS,LAB CHIM ORGANOELEMENTS,F-75252 PARIS 05,FRANCE
Tierney, JP
[1
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Alexakis, A
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UNIV PARIS 06,URA 473 CNRS,LAB CHIM ORGANOELEMENTS,F-75252 PARIS 05,FRANCEUNIV PARIS 06,URA 473 CNRS,LAB CHIM ORGANOELEMENTS,F-75252 PARIS 05,FRANCE
Alexakis, A
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]
Mangeney, P
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UNIV PARIS 06,URA 473 CNRS,LAB CHIM ORGANOELEMENTS,F-75252 PARIS 05,FRANCEUNIV PARIS 06,URA 473 CNRS,LAB CHIM ORGANOELEMENTS,F-75252 PARIS 05,FRANCE
Mangeney, P
[1
]
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[1] UNIV PARIS 06,URA 473 CNRS,LAB CHIM ORGANOELEMENTS,F-75252 PARIS 05,FRANCE
(R)-2-Cyclohexen-1-ol and (R)-2-cyclooctene-1-ol have been prepared in very good ee using R,R-homochiral bis-lithium amide bases derived from homochiral C-2 symmetric diamines. (R)-2-Cyclohexen-1-ol has been synthesized in good ee utilising catalytic homochiral bis-lithium amide in the presence of n-butyl lithium. (C) 1997 Elsevier Science Ltd.