Suzuki cross-coupling on enantiomerically pure epoxides: Efficient synthesis of diverse, modular amino alcohols from single enantiopure precursors

Journal of Organic Chemistry

Volumn 72, Issue 9, 2007, Pages 3253-3258

  Cattoën, Xavier ^a   Pericàs, Miquel A ^a,b  

^a INSTITUTE OF CHEMICAL RESEARCH OF CATALONIA ICIQ   (Spain)

^b UNIVERSITY OF BARCELONA   (Spain)

Author keywords

[No Author keywords available]

Indexed keywords

AMINO ALCOHOLS; ARYLGLYCIDYL ETHERS; BISOXAZOLINES; ENANTIOPURE PRECURSORS;

ALCOHOLS; ENANTIOMERS; ETHERS; MICROWAVE IRRADIATION; SYNTHESIS (CHEMICAL); TOLUENE;

EPOXY RESINS;

(3,5 DIBROMOPHENYL)GLYCIDYL ETHER DERIVATIVE; (4 BROMOPHENYL)GLYCIDYL ETHER DERIVATIVE; AMINOALCOHOL; BENZENE DERIVATIVE; BETA AMINOALCOHOL DERIVATIVE; CESIUM; CESIUM CARBONATE; OXAZOLINE DERIVATIVE; PALLADIUM; TOLUENE; UNCLASSIFIED DRUG;

ALCOHOL OXIDATION; AMMONIA FORMATION; ARTICLE; ARYLATION; ENANTIOMER; EPOXIDATION; MICROWAVE RADIATION; RING OPENING; STEREOSPECIFICITY; SUZUKI REACTION; SYNTHESIS;

EID: 34247570315     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo062612t     Document Type: Article

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34. These results will be reported in due course.