Convenient route to both enantiomers of a highly functionalized trans-disubstituted cyclopentene. Synthesis of the carbocyclic core of the nucleoside BCA

Journal of Organic Chemistry

Volumn 70, Issue 10, 2005, Pages 4199-4202

  Banerjee, Shyamapada ^a   Ghosh, Sarita ^a   Sinha, Saikat ^a   Ghosh, Subrata ^a  

^a DEPARTMENT OF MATERIALS SCIENCE   (India)

Author keywords

[No Author keywords available]

Indexed keywords

ALCOHOLS; AMINES; BIOLOGICAL MATERIALS; DERIVATIVES; OLEFINS;

AMINO CYCLOPENTENE; CYCLOPENTENOL; ENANTIOMERS; STEREOCONTROLLED SYNTHESIS;

SYNTHESIS (CHEMICAL);

ABACAVIR; CARBOVIR; CYCLOPENTENE DERIVATIVE; GLYCERALDEHYDE; NUCLEOSIDE DERIVATIVE; RNA DIRECTED DNA POLYMERASE INHIBITOR;

ACQUIRED IMMUNE DEFICIENCY SYNDROME; ANTIVIRAL ACTIVITY; ARTICLE; CHEMICAL MODIFICATION; DERIVATIZATION; ENANTIOMER; RING CLOSING METATHESIS; STEREOCHEMISTRY; STRUCTURE ANALYSIS; SYNTHESIS;

ADENINE; ANTI-HIV AGENTS; CYCLOPENTANES; NUCLEOSIDES; STEREOISOMERISM;

EID: 18744387239     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo0502504     Document Type: Article

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