Synthesis of 5′-O-phosphonomethyl-2′,3′-didehydro-2′,3′-dideoxyuridine by use of P-methoxybenzyl as a N3-protecting group.

Tetrahedron Letters

Volumn 32, Issue 16, 1991, Pages 1905-1908

  Van Aeroschot, A ^a   Jie, L ^a   Herdewijn, P ^a  

^a REGA INSTITUTE FOR MEDICAL RESEARCH   (Belgium)

Author keywords

[No Author keywords available]

Indexed keywords

2',3' DIDEHYDRO 2',3' DIDEOXY 5' O PHOSPHONOMETHYLURIDINE; ANTIVIRUS AGENT; UNCLASSIFIED DRUG; URIDINE DERIVATIVE;

ARTICLE; DRUG SYNTHESIS; PRIORITY JOURNAL;

EID: 0025974997     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(00)85994-8     Document Type: Article

References (11)

1. Regioselective reductive ring-opening of 4-methoxybenzylidene acetals of hexopyranosides. Access to a novel protecting-group strategy. Part 1
2. Synthesis of 5'-O-phosphonomethyl derivatives of pyrimidine 2'-deoxynucleosides
3. 5-Fluorouracil derivatives. Part XVIII. p-Methoxybenzyl as a new N3-imide protecting group of 5-fluorouridine and its application to the synthes of 5'-O-acryloyl-5-fluorouridine.