Nucleophilic openings of bicyclic β-lactones via acyl C-O and alkyl C-O cleavage: Catalytic, asymmetric synthesis of a versatile, carbocyclic nucleoside precursor and protected transpentacin

Tetrahedron

Volumn 58, Issue 35, 2002, Pages 7075-7080

  Yokota, Yasuno ^a   Cortez, Guillermo S ^a   Romo, Daniel ^a  

^a TEXAS A AND M UNIVERSITY   (United States)

Author keywords

Bicyclic lactone; Nucleophile catalyzed aldol lactonization process; Nucleophilic ring openings

Indexed keywords

ALUMINUM; BORON; CARBOCYCLIC NUCLEOSIDE; CARBOXYLIC ACID DERIVATIVE; CYCLOPENTANE; HYDROXYLAMINE; LACTONE DERIVATIVE; PENTETATE CALCIUM TRISODIUM; REAGENT;

ALDOL REACTION; ARTICLE; ASYMMETRIC SYNTHESIS; CATALYSIS; CHEMICAL BOND; CHEMICAL REACTION; DEGRADATION; ENVIRONMENTAL TEMPERATURE; MOLECULAR DYNAMICS; PRIORITY JOURNAL; REDUCTION;

EID: 0037178969     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4020(02)00703-2     Document Type: Article

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