Mechanism and optimisation of the homoboroproline bifunctional catalytic asymmetric aldol reaction: Lewis acid tuning through in situ esterification

Organic and Biomolecular Chemistry

Volumn 10, Issue 12, 2012, Pages 2422-2430

  Georgiou, Irene ^a   Whiting, Andrew ^a  

^a DURHAM UNIVERSITY   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ALDOL REACTIONS; ASYMMETRIC ALDOL REACTIONS; BI-FUNCTIONAL CATALYSTS; BIFUNCTIONAL; BORONATE; BORONATE ESTERS; CYCLOHEXYL; IN-SITU; LEWIS ACID; LEWIS ACIDITY; MODE OF ACTION; OPTIMISATIONS; TARTRATE ESTERS;

BORON; CATALYSTS; CONDENSATION REACTIONS; ESTERIFICATION; OPTIMIZATION;

ESTERS;

3-HYDROXYBUTANAL; ALDEHYDE; ALDOL; DRUG DERIVATIVE; LEWIS ACID; PIPECOLIC ACID; PROLINE;

ARTICLE; CATALYSIS; CHEMICAL STRUCTURE; CHEMISTRY; ESTERIFICATION; STEREOISOMERISM;

ALDEHYDES; CATALYSIS; ESTERIFICATION; LEWIS ACIDS; MOLECULAR STRUCTURE; PROLINE; STEREOISOMERISM;

EID: 84858051162     PISSN: 14770520     EISSN: None     Source Type: Journal    
DOI: 10.1039/c2ob06872a     Document Type: Article

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