A versatile route to functionalized dilactones as monomers for the synthesis of poly(α-hydroxy) acids

European Journal of Organic Chemistry

Volumn , Issue 17, 2003, Pages 3344-3349

  Leemhuis, Mark ^a   Van Steenis, Jan Hein ^a   Van Uxem, Michelle J ^a   Van Nostrum, Cornelus F ^a   Hennink, Wim E ^a  

^a UTRECHT UNIVERSITY   (Netherlands)

Author keywords

Lactide; Lactones; Polymers; Synthetic methods; Hydroxy acids

Indexed keywords

2 BENZYLOXYMETHYL 5 METHYLGLYCOLIDE; 2 HYDROXYACID; BENZYLOXYMETHYLGLYCOLIDE; CHLORIDE; CYANURIC ACID; CYANURIC CHLORIDE; DILACTONE DERIVATIVE; DIMER; GLYCOLIC ACID DERIVATIVE; LACTONE DERIVATIVE; METHYLGLYCOLIDE; MONOMER; POLY(2 HYDROXYACID); UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL ANALYSIS; CHEMICAL REACTION; CHEMICAL STRUCTURE; CYCLIZATION; DRUG SYNTHESIS; POLYMERIZATION; REACTION ANALYSIS; RING CLOSING METATHESIS; STRUCTURE ANALYSIS; SUBSTITUTION REACTION; TECHNIQUE;

EID: 0043287141     PISSN: 1434193X     EISSN: None     Source Type: Journal    
DOI: 10.1002/ejoc.200300181     Document Type: Article

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