A new protecting group '3′,5′-O-sulfinyl' for xylo-nucleosides. A simple and efficient synthesis of 3′-amino-3′-deoxyadenosine (a puromycin intermediate), 2,2′-anhydro-pyrimidine nucleosides and 2′,3′-anhydro-adenosine

Tetrahedron Letters

Volumn 45, Issue 1, 2004, Pages 137-140

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

^a Ichikawa Research Institute   (Japan)

^b CHIBA UNIVERSITY   (Japan)

Author keywords

3 ,5 O sulfinyl xylo nucleosides; 3 amino 3 deoxyadenosine; Puromycin

Indexed keywords

2',3' ANHYDROADENOSINE; 3' AMINO 3' DEOXYADENOSINE; ADENOSINE DERIVATIVE; CARBAMIC ACID DERIVATIVE; CHLORIDE; CORDYCEPIN DERIVATIVE; NUCLEOSIDE DERIVATIVE; PUROMYCIN; PYRIMIDINE NUCLEOSIDE; UNCLASSIFIED DRUG; URIDINE DERIVATIVE;

ARTICLE; CYCLIZATION; DEPROTECTION REACTION;

EID: 0842308215     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2003.10.092     Document Type: Article

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