An efficient synthesis of 7-functionalized 7-deazapurine β-D- or β-L-ribonucleosides: Glycosylation of pyrrolo[2,3-d]pyrimidines with 1-O-acetyl-2,3,5-tri-o-benzoyl-D-or L-ribofuranose

Nucleosides, Nucleotides and Nucleic Acids

Volumn 26, Issue 6-7, 2007, Pages 603-606

  Peng, Xiaohua ^c   Seela, Frank ^a,b  

^a UNIVERSITY OF OSNABRÜCK   (Germany)

^b UNIVERSITY OF MÜNSTER   (Germany)

^c NONE

Author keywords

7 deazapurines; Functionalization; Glycosylation; Pyrrolo 2,3 d pyrimidines; Ribonucleosides; Silyl Hilbert Johnson reaction

Indexed keywords

1 O ACETYL 2,3,5 TRI O BENZOYL; 7 DEAZAPURINE; BETA RIBONUCLEOSIDE; NUCLEOSIDE DERIVATIVE; PYRROLO[2,3 D]PYRIMIDINE DERIVATIVE; RIBOFURANOSE; RIBONUCLEOSIDE; UNCLASSIFIED DRUG;

AMINO ACID SYNTHESIS; CHEMICAL ANALYSIS; CONFERENCE PAPER; GLYCOSYLATION;

CATALYSIS; GLYCOSYLATION; MONOSACCHARIDES; PALLADIUM; PURINES; PYRIMIDINES; RIBONUCLEOSIDES;

EID: 36949035133     PISSN: 15257770     EISSN: 15322335     Source Type: Journal    
DOI: 10.1080/15257770701490332     Document Type: Conference Paper

References (9)

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