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Organic and Biomolecular Chemistry

Volumn 9, Issue 22, 2011, Pages 7655-7658

Deuterium-isotope study on the reductive ring opening of benzylidene acetals

(5) Lee, I Chi a Zulueta, Medel Manuel L a,b Shie, Chi Rung a Arco, Susan D b Hung, Shang Cheng a,c

a GENOMICS RESEARCH CENTER (Taiwan)

b University of the Philippines Diliman (Philippines)

c NATIONAL CHIAO TUNG UNIVERSITY (Taiwan)

Author keywords

[No Author keywords available]

Indexed keywords

BENZYLIDENE ACETALS; NUCLEOPHILIC SUBSTITUTIONS; REFERENCE COMPOUNDS; REGIO-SELECTIVE; RING OPENING;

CARBOHYDRATES; DEUTERIUM; STEREOSELECTIVITY;

DEUTERIUM COMPOUNDS;

ACETAL DERIVATIVE; ALUMINUM DERIVATIVE; ALUMINUM LITHIUM HYDRIDE; BENZYLIDENE DERIVATIVE; DEUTERIUM; HYDROXIDE; HYDROXIDE ION; LITHIUM DERIVATIVE;

ARTICLE; CHEMISTRY; GLYCOSYLATION; METHODOLOGY; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; ORGANIC CHEMISTRY; OXIDATION REDUCTION REACTION; STEREOISOMERISM;

ACETALS; ALUMINUM COMPOUNDS; BENZYLIDENE COMPOUNDS; CHEMISTRY, ORGANIC; DEUTERIUM; GLYCOSYLATION; HYDROXIDES; LITHIUM COMPOUNDS; MAGNETIC RESONANCE SPECTROSCOPY; OXIDATION-REDUCTION; STEREOISOMERISM;

EID: 80054996701 PISSN: 14770520 EISSN: None Source Type: Journal
DOI: 10.1039/c1ob06056b Document Type: Article

Times cited : (18)

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