Elaboration of D-(-)-ribose into a tricyclic, natural product-like scaffold

Journal of Organic Chemistry

Volumn 69, Issue 24, 2004, Pages 8558-8560

  Messer, Roland ^a   Schmitz, Andrea ^a   Moesch, Luzia ^a   Häner, Robert ^a  

^a UNIVERSITY OF BERN   (Switzerland)

Author keywords

[No Author keywords available]

Indexed keywords

CHEMICAL MODIFICATION; DERIVATIVES; MOLECULAR DYNAMICS; MOLECULAR STRUCTURE; REACTION KINETICS; SCAFFOLDS; STEREOCHEMISTRY; X RAY ANALYSIS;

DIASTEREOSELECTIVITY; INTRAMOLECULAR HETERO-DIELS-ALDER REACTION; TRICYCLIC SCAFFOLDS; X-RAY STRUCTURAL ANALYSIS;

ORGANIC COMPOUNDS;

DIHYDROFURANE; NATURAL PRODUCT; RIBOSE; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL MODIFICATION; CHEMICAL STRUCTURE; DERIVATIZATION; DIASTEREOISOMER; DIELS ALDER REACTION; REACTION ANALYSIS; STEREOCHEMISTRY;

CRYSTALLOGRAPHY, X-RAY; FURANS; MOLECULAR CONFORMATION; POLYMERS; RIBOSE; STEREOISOMERISM;

EID: 9344228493     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo048351+     Document Type: Article

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