A simple and efficient synthesis of puromycin, 2,2′-anhydro- pyrimidine nucleosides, cytidines and 2′,3′-anhydroadenosine from 3′,5′-O-sulfinyl xylo-nucleosides

Nucleosides, Nucleotides and Nucleic Acids

Volumn 25, Issue 7, 2006, Pages 719-734

  Takatsuki, Ken Ichi ^a,b   Ohgushi, Sumito ^b   Kohmoto, Shigeo ^b   Kishikawa, Keiki ^b   Yamamoto, Makoto ^b  

^a Ichikawa Research Institute   (Japan)

^b CHIBA UNIVERSITY   (Japan)

Author keywords

2,2 Anhydro pyrimidine Nucleoside; 3 ,5 O sulfinyl xylo nucleosides; Puromycin

Indexed keywords

2',3' ANHYDROADENOSINE; 2,2' ANHYDROPYRIMIDINE NUCLEOSIDE DERIVATIVE; 3',5' O SULFINYL XYLONUCLEOSIDE DERIVATIVE; ADENOSINE DERIVATIVE; ANTIBIOTIC AGENT; CARBAMIC ACID DERIVATIVE; CYTIDINE DERIVATIVE; NUCLEOSIDE DERIVATIVE; PUROMYCIN; SULFITE; UNCLASSIFIED DRUG;

ARTICLE; CYCLIZATION; DEPROTECTION REACTION; DRUG STRUCTURE; DRUG SYNTHESIS;

ADENOSINE; CYCLIZATION; CYTIDINE; DEOXYADENOSINES; NUCLEIC ACID CONFORMATION; NUCLEOSIDES; PUROMYCIN; PYRIMIDINE NUCLEOSIDES; STEREOISOMERISM; SULFUR ACIDS;

EID: 33746857294     PISSN: 15257770     EISSN: 15322335     Source Type: Journal    
DOI: 10.1080/15257770600725929     Document Type: Article

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