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Organic and Biomolecular Chemistry

Volumn 10, Issue 28, 2012, Pages 5456-5465

Synthesis of anti-HIV lithospermic acid by two diverse strategies

(2) Varadaraju, Tirumala G a Hwu, Jih Ru a,b

a NATIONAL TSING HUA UNIVERSITY (Taiwan)

b NATIONAL CENTRAL UNIVERSITY (Taiwan)

Author keywords

[No Author keywords available]

Indexed keywords

ALDOL CONDENSATION; ANTI-HIV; ANTI-HIV ACTIVITY; CARBON-CARBON DOUBLE BONDS; CINNAMIC ACIDS; LITHOSPERMIC ACID; METHYL LACTATE; NATURAL PRODUCTS; PALLADIUM-CATALYZED; STEREOSELECTIVE REDUCTION; TOTAL SYNTHESIS;

CONDENSATION REACTIONS; MERCURY COMPOUNDS; ORGANIC POLLUTANTS;

AROMATIC COMPOUNDS;

3,4 DIMETHOXYBENZALDEHYDE; 3,4-DIMETHOXYBENZALDEHYDE; ANTI HUMAN IMMUNODEFICIENCY VIRUS AGENT; BENZALDEHYDE DERIVATIVE; BENZOFURAN DERIVATIVE; BIOLOGICAL PRODUCT; DEPSIDE; LITHOSPERMIC ACID; PALLADIUM;

ARTICLE; CATALYSIS; CHEMISTRY; CYCLIZATION; HUMAN; HUMAN IMMUNODEFICIENCY VIRUS INFECTION; STEREOISOMERISM; SYNTHESIS;

ANTI-HIV AGENTS; BENZALDEHYDES; BENZOFURANS; BIOLOGICAL AGENTS; CATALYSIS; CYCLIZATION; DEPSIDES; HIV INFECTIONS; HUMANS; PALLADIUM; STEREOISOMERISM;

EID: 84863607222 PISSN: 14770520 EISSN: None Source Type: Journal
DOI: 10.1039/c2ob25575h Document Type: Article

Times cited : (28)

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