cheminform abstract: enantioselective synthesis of imperanene, a platelet aggregation inhibitor

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2002 other bioactive products other bioactive products U 1300 04 - 246 Enantioselective Synthesis of Imperanene, a Platelet Aggregation Inhibitor. Both enantiomers of imperanene (VIII) are accessible using Enders’ SAMP/RAMP chiral auxiliary method for the diastereoselective alkylation of aldehyde (II). After removal of the chiral auxiliary, the optical purity of the alkylation product (VII) and its enantiomer is determined to be 82-90% e.e. Comparison of the data of enantiomers (R)- and (S)-(VIII) with those of previously isolated imperanene reveals the (S)-enantiomer to be the naturally occurring isomer. — (SHATTUCK, JAMES C.; SHREVE, CHENEY M.; SOLOMON, SANDRA E.; Org. Lett. 3 (2001) 19, 3021-3023; Dep. Chem., Univ. Hartford, West Hartford, CT 06117, USA; EN) 1

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2002 other bioactive products

other bioactive productsU 1300

04 - 246Enantioselective Synthesis of Imperanene, a Platelet AggregationInhibitor. — Both enantiomers of imperanene (VIII) are accessibleusing Enders’ SAMP/RAMP chiral auxiliary method for the diastereoselectivealkylation of aldehyde (II). After removal of the chiral auxiliary, the opticalpurity of the alkylation product (VII) and its enantiomer is determined tobe 82-90% e.e. Comparison of the data of enantiomers (R)- and (S)-(VIII)with those of previously isolated imperanene reveals the (S)-enantiomer tobe the naturally occurring isomer. — (SHATTUCK, JAMES C.; SHREVE,CHENEY M.; SOLOMON, SANDRA E.; Org. Lett. 3 (2001) 19, 3021-3023;Dep. Chem., Univ. Hartford, West Hartford, CT 06117, USA; EN)

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