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Chemistry - A European Journal

Volumn 19, Issue 51, 2013, Pages 17584-17588

Trapped in misbelief for almost 40 years: Selective synthesis of the four stereoisomers of mefloquine

(5) Schützenmeister, Nina a Müller, Michael a Reinscheid, Uwe M a Griesinger, Christian a Leonov, Andrei a

a MAX PLANCK INSTITUTE FOR BIOPHYSICAL CHEMISTRY (Germany)

Author keywords

domino reactions; drug design; mefloquine; structure elucidation; total synthesis

Indexed keywords

DOMINO REACTIONS; DRUG DESIGN; MEFLOQUINE; STRUCTURE ELUCIDATION; TOTAL SYNTHESIS;

ENANTIOMERS; PHYSICAL CHEMISTRY; REACTION KINETICS; STEREOCHEMISTRY; SYNTHESIS (CHEMICAL);

MALARIA CONTROL;

ANTIMALARIAL AGENT; MEFLOQUINE;

ARTICLE; CHEMISTRY; DOMINO REACTIONS; DRUG DESIGN; STEREOISOMERISM; STRUCTURE ELUCIDATION; SYNTHESIS; TOTAL SYNTHESIS;

DOMINO REACTIONS; DRUG DESIGN; MEFLOQUINE; STRUCTURE ELUCIDATION; TOTAL SYNTHESIS;

ANTIMALARIALS; DRUG DESIGN; MEFLOQUINE; STEREOISOMERISM;

EID: 84890121337 PISSN: 09476539 EISSN: 15213765 Source Type: Journal
DOI: 10.1002/chem.201303403 Document Type: Article

Times cited : (16)

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