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Organic and Biomolecular Chemistry

Volumn 8, Issue 21, 2010, Pages 4831-4833

Asymmetric synthesis of a tricyclic benzofuran motif: A privileged core structure in biologically active molecules

(2) Sundén, Henrik a Olsson, Roger a,b

a UNIVERSITY OF GOTHENBURG (Sweden)

b ACADIA Pharmaceuticals AB (Sweden)

Author keywords

[No Author keywords available]

Indexed keywords

ASYMMETRIC SYNTHESIS; BENZOFURANS; BIOLOGICALLY ACTIVE MOLECULES; CHIRAL REDUCTION; CORE STRUCTURE; HECK REACTIONS; MITSUNOBU REACTIONS; OXAZABOROLIDINE; REDUCTION YIELD; STEREOGENIC CENTERS; SYNTHETIC STRATEGIES; TARGET MOLECULE;

MOLECULES; PALLADIUM; STEREOCHEMISTRY;

SYNTHESIS (CHEMICAL);

BENZOFURAN DERIVATIVE;

ARTICLE; CATALYSIS; CHEMICAL STRUCTURE; CHEMISTRY; STEREOISOMERISM; SYNTHESIS;

BENZOFURANS; CATALYSIS; MOLECULAR STRUCTURE; STEREOISOMERISM;

EID: 77957899918 PISSN: 14770520 EISSN: None Source Type: Journal
DOI: 10.1039/c0ob00331j Document Type: Article

Times cited : (18)

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