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Volumn 67, Issue 5, 2002, Pages 1669-1677

Development of versatile cis- and trans-dicarbon-substituted chiral cyclopropane units: Synthesis of (1S,2R)- and (1R,2R)-2-aminomethyl-1-(1H-imidazol-4-yl)cyclopropanes and their enantiomers as conformationally restricted analogues of histamine

(3) Kazuta, Yuji a Matsuda, Akira a Shuto, Satoshi a

a HOKKAIDO UNIVERSITY (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

KEY INTERMEDIATES;

AMINES; CARBON; CONFORMATIONS; SULFONATION; SYNTHESIS (CHEMICAL);

PROPANE;

2 (TERT BUTYLDIPHENYLSILYLOXY)METHYL 1 FORMYLCYCLOPROPANE; 2 AMINOMETHYL 1 (1H IMIDAZOL 4 YL)CYCLOPROPANE; ACETONITRILE DERIVATIVE; ALCOHOL; CYCLOPROPANE DERIVATIVE; EPICHLOROHYDRIN; HISTAMINE DERIVATIVE; MAGNESIUM; METHANOL; N METHYL DEXTRO ASPARTIC ACID RECEPTOR BLOCKING AGENT; PHENYLSULFONYLACETONITRILE; UNCLASSIFIED DRUG;

ARTICLE; CHIRALITY; CIS TRANS ISOMERISM; DRUG CONFORMATION; DRUG SYNTHESIS; ENANTIOMER; GEL CHROMATOGRAPHY; PROTON NUCLEAR MAGNETIC RESONANCE;

CHROMATOGRAPHY; CYCLOPROPANES; HISTAMINE; IMIDAZOLES; MAGNETIC RESONANCE SPECTROSCOPY; MOLECULAR STRUCTURE; STEREOISOMERISM;

EID: 0037040657 PISSN: 00223263 EISSN: None Source Type: Journal
DOI: 10.1021/jo010852x Document Type: Article

Times cited : (82)

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