Synthetic studies of liposidomycin degradation product: Attempt for introduction of an uracil group

Heterocycles

Volumn 66, Issue 1, 2005, Pages 129-134

  Fukunishi, Shouhei ^a   Ubukata, Makoto ^b   Nakajima, Noriyuki ^a  

^a TOYAMA PREFECTURAL UNIVERSITY   (Japan)

^b HOKKAIDO UNIVERSITY   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 33646860560     PISSN: 03855414     EISSN: None     Source Type: Journal    
DOI: 10.3987/COM-05-S(K)47     Document Type: Article

References (24)

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21. Compound 22 was made from the methyl 2,3-isopropylidene-β-d-ribofuranoside (29) via 30 in following three step sequences: the coupling with O-nitrobenzenesulfonyl benzyl amine under Mitsunobu conditions, deprotection of methyl acetal and acetonide by 1N HCl, and the acetyl protection. {A figure is presented}
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