Ring-closing metathesis-based synthesis of (3R,4R,5S)-4-acetylamino-5- amino-3-hydroxy-cyclohex-1-ene-carboxylic acid ethyl ester: A functionalized cycloalkene skeleton of GS4104

Journal of Organic Chemistry

Volumn 71, Issue 14, 2006, Pages 5365-5368

  Cong, Xin ^a   Yao, Zhu Jun ^a  

^a SHANGHAI INSTITUTE OF ORGANIC CHEMISTRY   (China)

Author keywords

[No Author keywords available]

Indexed keywords

DIASTEREOSELECTIVELY; METATHESIS; QUINIC ACID; SHIKIMIC ACID;

CARBOXYLIC ACIDS; NITROGEN COMPOUNDS; NUCLEAR MAGNETIC RESONANCE; REACTION KINETICS; STEREOCHEMISTRY; SYNTHESIS (CHEMICAL);

ESTERS;

4 ACETYLAMINO 5 AMINO 3 HYDROXYCYCLOHEX 1 ENE CARBOXYLIC ACID ETHYL ESTER; ANTIVIRUS AGENT; CARBOXYLIC ACID DERIVATIVE; CYCLOALKENE; OSELTAMIVIR; UNCLASSIFIED DRUG; ZANAMIVIR;

ANTIVIRAL ACTIVITY; ARTICLE; CARBON NUCLEAR MAGNETIC RESONANCE; DRUG STRUCTURE; DRUG SYNTHESIS; ELECTROSPRAY MASS SPECTROMETRY; INFLUENZA; NONHUMAN; PROTON NUCLEAR MAGNETIC RESONANCE; RING CLOSING METATHESIS;

CYCLIZATION; CYCLOHEXENES; CYCLOPARAFFINS; ESTERS; MOLECULAR CONFORMATION; OSELTAMIVIR; STEREOISOMERISM;

EID: 33745700294     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo060633h     Document Type: Article

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