ENANTIOMERICALLY PURE CYCLOALKENYLACETIC-ACID DERIVATIVES VIA PD-CATALYZED ASYMMETRIC ALLYLIC ALKYLATION AND SUBSEQUENT ENANTIOMERIC ENRICHMENT VIA IODOLACTONES
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SENNHENN, P
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UNIV HEIDELBERG,INST ORGAN CHEM,D-69120 HEIDELBERG,GERMANYUNIV HEIDELBERG,INST ORGAN CHEM,D-69120 HEIDELBERG,GERMANY
SENNHENN, P
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GABLER, B
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UNIV HEIDELBERG,INST ORGAN CHEM,D-69120 HEIDELBERG,GERMANYUNIV HEIDELBERG,INST ORGAN CHEM,D-69120 HEIDELBERG,GERMANY
GABLER, B
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HELMCHEN, G
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UNIV HEIDELBERG,INST ORGAN CHEM,D-69120 HEIDELBERG,GERMANYUNIV HEIDELBERG,INST ORGAN CHEM,D-69120 HEIDELBERG,GERMANY
HELMCHEN, G
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[1] UNIV HEIDELBERG,INST ORGAN CHEM,D-69120 HEIDELBERG,GERMANY
Chiral (phosphinoaryl-oxazoline)Pd complexes with stereogenic phosphorus were used as catalysts for alkylation of cycloalkenyl acetates which gave products with up to 85% ee. Excellent reactivity allowed reactions with as little as 0.02 mol% of Pd. Five- and six-membered ring synthons of interest for syntheses of biologically active compounds with > 99% ee were obtained via recrystallization of iodolactones.