Total selective synthesis of enantiopure O1-acyl-3-aminoalkane- 1,2-diols by ring opening of aminoepoxides with carboxylic acids

Journal of Organic Chemistry

Volumn 70, Issue 25, 2005, Pages 10348-10353

  Concellón, José M ^a   Suárez, José Ramón ^a   Del Solar, Virginia ^a   Llavona, Ricardo ^a  

^a UNIVERSITY OF OVIEDO   (Spain)

Author keywords

[No Author keywords available]

Indexed keywords

CARBOXYLIC ACIDS; CATALYST SELECTIVITY; REACTION KINETICS; SYNTHESIS (CHEMICAL);

CHLOROTRIMETHYLSILANES; REACTION CONDITIONS; TOTAL SELECTIVE SYNTHESIS; TOTAL SELECTIVITY;

AROMATIC COMPOUNDS;

2 (1 DIBENZYLAMINOETHYL)EPOXIDE; ALKANEDIOL DERIVATIVE; CARBOXYLIC ACID; EPOXIDE; ESTER; UNCLASSIFIED DRUG;

ARTICLE; CARBON NUCLEAR MAGNETIC RESONANCE; CHEMICAL REACTION; CHEMICAL STRUCTURE; PROTON NUCLEAR MAGNETIC RESONANCE; RING OPENING; SYNTHESIS;

AMINO ALCOHOLS; CARBOXYLIC ACIDS; EPOXY COMPOUNDS; STEREOISOMERISM;

EID: 28744454683     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo0514873     Document Type: Article

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