Synthesis of 2′,3′-dideoxy-6′-fluorocarbocyclic nucleosides via Reformatskii-Claisen rearrangement

Tetrahedron

Volumn 67, Issue 19, 2011, Pages 3388-3394

  Yang, Yi ^a   Zheng, Feng ^a   Qing, Feng Ling ^a,b  

^a SHANGHAI INSTITUTE OF ORGANIC CHEMISTRY   (China)

^b DONGHUA UNIVERSITY   (China)

Author keywords

Fluorinated carbocyclic nucleosides; Mitsunobu reaction; Reformatskii Claisen rearrangement; Ring closing metathesis

Indexed keywords

1 [5 FLUORO 4 (HYDROXYMETHYL)CYCLOPENT 2 ENYL] 5 METHYLPYRIMIDINE 2,4(1H,3H) DIONE; 1 [5 FLUORO 4 (HYDROXYMETHYL)CYCLOPENT 2 ENYL]PYRIMIDINE 2,4(1H,3H) DIONE; 2',3' DIDEOXY 6' FLUOROCARBOCYCLIC NUCLEOSIDE; [4 (6 AMINO 9H PURIN 9 YL) 5 FLUOROCYCLOPENT 2 ENYL]METHANOL; ABACAVIR; CARBOVIR; FLUORINATED CARBOCYCLIC NUCLEOSIDE; NUCLEOSIDE DERIVATIVE; SILICON; UNCLASSIFIED DRUG;

ARTICLE; CARBON NUCLEAR MAGNETIC RESONANCE; CHEMICAL REACTION; CHEMICAL STRUCTURE; FLUORINATION; MITSUNOBU REACTION; PRIORITY JOURNAL; PROTON NUCLEAR MAGNETIC RESONANCE; REFORMATSKIIE CLAISEN REARRANGEMENT; RING CLOSING METATHESIS; SYNTHESIS;

EID: 79955039548     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2011.03.054     Document Type: Article

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