SULFUR DERIVATIVES OF EPHEDRA ALKALOIDS - NEW AND HIGHLY EFFICIENT CHIRAL CATALYSTS
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HOF, RP
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UNIV GRONINGEN,DEPT ORGAN & MOLEC INORGAN CHEM,9747 AG GRONINGEN,NETHERLANDSUNIV GRONINGEN,DEPT ORGAN & MOLEC INORGAN CHEM,9747 AG GRONINGEN,NETHERLANDS
HOF, RP
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POELERT, MA
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UNIV GRONINGEN,DEPT ORGAN & MOLEC INORGAN CHEM,9747 AG GRONINGEN,NETHERLANDSUNIV GRONINGEN,DEPT ORGAN & MOLEC INORGAN CHEM,9747 AG GRONINGEN,NETHERLANDS
POELERT, MA
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PEPER, NCMW
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UNIV GRONINGEN,DEPT ORGAN & MOLEC INORGAN CHEM,9747 AG GRONINGEN,NETHERLANDSUNIV GRONINGEN,DEPT ORGAN & MOLEC INORGAN CHEM,9747 AG GRONINGEN,NETHERLANDS
PEPER, NCMW
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KELLOGG, RM
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UNIV GRONINGEN,DEPT ORGAN & MOLEC INORGAN CHEM,9747 AG GRONINGEN,NETHERLANDSUNIV GRONINGEN,DEPT ORGAN & MOLEC INORGAN CHEM,9747 AG GRONINGEN,NETHERLANDS
KELLOGG, RM
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[1] UNIV GRONINGEN,DEPT ORGAN & MOLEC INORGAN CHEM,9747 AG GRONINGEN,NETHERLANDS
Sulfur derivatives of ephedrine catalyze the 1,2-addition of diethylzinc to benzaldehyde in high enantiomeric excess. Disulfides and cyclic sulfide derivatives of these compounds serve the purpose Very well, and the actual catalytically active species, containing zinc, has been extracted from the reaction mixture.
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STATE UNIV GRONINGEN, DEPT ORGAN CHEM, NIJENBORGH 16, 9747 AG GRONINGEN, NETHERLANDSSTATE UNIV GRONINGEN, DEPT ORGAN CHEM, NIJENBORGH 16, 9747 AG GRONINGEN, NETHERLANDS
SMAARDIJK, AA
WYNBERG, H
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STATE UNIV GRONINGEN, DEPT ORGAN CHEM, NIJENBORGH 16, 9747 AG GRONINGEN, NETHERLANDSSTATE UNIV GRONINGEN, DEPT ORGAN CHEM, NIJENBORGH 16, 9747 AG GRONINGEN, NETHERLANDS
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STATE UNIV GRONINGEN, DEPT ORGAN CHEM, NIJENBORGH 16, 9747 AG GRONINGEN, NETHERLANDSSTATE UNIV GRONINGEN, DEPT ORGAN CHEM, NIJENBORGH 16, 9747 AG GRONINGEN, NETHERLANDS
SMAARDIJK, AA
WYNBERG, H
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h-index: 0
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STATE UNIV GRONINGEN, DEPT ORGAN CHEM, NIJENBORGH 16, 9747 AG GRONINGEN, NETHERLANDSSTATE UNIV GRONINGEN, DEPT ORGAN CHEM, NIJENBORGH 16, 9747 AG GRONINGEN, NETHERLANDS