An efficient synthesis of 7-functionalized 7-deazapurine beta-D- Or beta-L-ribonucleosides: glycosylation of pyrrolo[2,3-D]pyrimidines with 1-O-acetyl-2,3,5-tri-O-benzoyl-D-Or L-ribofuranose

Xiaohua Peng; Frank Seela

doi:10.1080/15257770701490332

An efficient synthesis of 7-functionalized 7-deazapurine beta-D- Or beta-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 Nucleic Acids. 2007;26(6-7):603-6. doi: 10.1080/15257770701490332.

Authors

Xiaohua Peng¹, Frank Seela

Affiliation

¹ Laboratorium für Organische und Bioorganische Chemie, Universität Osnabrück, Osnabrück, Germany.

PMID: 18066863
DOI: 10.1080/15257770701490332

Abstract

The glycosylation reaction performed with 7-halogenated 7-deazapurines employing commercially available 1-O-acetyl-2,3,5-tri-O-benzoyl-D- or L-ribofuranoses is described.

MeSH terms

Catalysis
Glycosylation
Monosaccharides / chemistry*
Palladium
Purines / chemical synthesis*
Purines / chemistry
Pyrimidines / chemistry*
Ribonucleosides / chemical synthesis*
Ribonucleosides / chemistry

Substances

1-O-acetyl-2,3,5-tri-O-benzoyl-D-ribofuranose
7-deazapurine
Monosaccharides
Purines
Pyrimidines
Ribonucleosides
Palladium