Synthesis of deoxy sugar esters: A chemoenzymatic stereoselective approach affording deoxy sugar derivatives also in the form of aldehyde

Journal of Organic Chemistry

Volumn 72, Issue 15, 2007, Pages 5813-5816

  Villo, Ly ^a   Danilas, Kady ^a   Metsala, Andrus ^a   Kreen, Malle ^a   Vallikivi, Imre ^b   Vija, Sirje ^c   Pehk, Tõnis ^c   Saso, Luciano ^d   Parve, Omar ^a  

^a TALLINN UNIVERSITY OF TECHNOLOGY   (Estonia)

^b UNIVERSITY OF TARTU   (Estonia)

^c NATIONAL INSTITUTE OF CHEMICAL PHYSICS AND BIOPHYSICS   (Estonia)

^d SAPIENZA UNIVERSITY OF ROME   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

ALCOHOLIC HYDROXYL; CHEMOENZYMATIC STEREOSELECTIVE APPROACH; MANDELIC ACID DERIVATIVES;

ACETYLATION; ALDEHYDES; CARBOXYLIC ACIDS; NUCLEAR MAGNETIC RESONANCE; SUGAR (SUCROSE); SYNTHESIS (CHEMICAL);

ESTERS;

2 BROMO 5 ACETOXYPENTANAL; ACETAL DERIVATIVE; ALDEHYDE; BROMINE DERIVATIVE; CARBOXYLIC ACID; DEOXYSUGAR; ESTER DERIVATIVE; HYDROXYL GROUP; MANDELIC ACID DERIVATIVE; TRIACYLGLYCEROL LIPASE; UNCLASSIFIED DRUG;

ACETYLATION; ALKYLATION; ANALYTIC METHOD; ARTICLE; CHEMICAL REACTION; NUCLEAR MAGNETIC RESONANCE; REACTION ANALYSIS; STEREOCHEMISTRY; SYNTHESIS;

ALDEHYDES; DEOXY SUGARS; ESTERS; MAGNETIC RESONANCE SPECTROSCOPY; MASS SPECTROMETRY;

EID: 34547098578     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo062640b     Document Type: Article

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