Cyclobutane amino acid analogues of furanomycin obtained by a formal [2 + 2] cycloaddition strategy promoted by methylaluminoxane

Journal of Organic Chemistry

Volumn 75, Issue 3, 2010, Pages 545-552

  Avenoza, Alberto ^a   Busto, Jesús H ^a   Canal, Noelia ^a   Corzana, Francisco ^a   Peregrina, Jesús M ^a   Pérez Fernández, Marta ^a   Rodríguez, Fernando ^a  

^a UNIVERSITY OF LA RIOJA   (Spain)

Author keywords

[No Author keywords available]

Indexed keywords

[2 + 2] CYCLOADDITION; CHEMICAL EQUATIONS; CONFORMATIONAL ANALYSIS; CYCLOBUTANES; DIHYDROFURANS; LEWIS ACID; METHYLALUMINOXANE; NATURAL PRODUCTS; SYNTHETIC STRATEGIES; TETRA-HYDROFURAN;

AMINO ACIDS; BUTANE; OLEFINS; ORGANIC ACIDS;

SYNTHESIS (CHEMICAL);

2 (ACYLAMINO)ACRYLATE DERIVATIVE; ACRYLIC ACID DERIVATIVE; ALUMINUM DERIVATIVE; AMINO ACID; ANTIBIOTIC AGENT; CYCLOBUTANE DERIVATIVE; FURANOMYCIN; METHYLALUMINOXANE; TETRAHYDROFURAN DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; CONFORMATIONAL TRANSITION; CRYSTAL STRUCTURE; CYCLOADDITION;

ALUMINUM COMPOUNDS; AMINO ACIDS; CATALYSIS; CRYSTALLOGRAPHY, X-RAY; CYCLIZATION; CYCLOBUTANES; MAGNETIC RESONANCE SPECTROSCOPY; MOLECULAR CONFORMATION; STEREOISOMERISM; STRUCTURE-ACTIVITY RELATIONSHIP;

EID: 75749129442     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo9025258     Document Type: Article

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