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Volumn 71, Issue 25, 2006, Pages 9420-9430

Synthesis of methylene- and difluoromethylenephosphonate analogues of uridine-4-phosphate and 3-deazauridine-4-phosphate

Author keywords

[No Author keywords available]

Indexed keywords

AMINO ACIDS; CHEMICAL MODIFICATION; ENZYME INHIBITION; ENZYMES; ESTERS; OXYGEN; PHOSPHATES;

EID: 33845514316     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo0617666     Document Type: Article
Times cited : (20)

References (50)
  • 47
    • 33845544366 scopus 로고    scopus 로고
    • note
    • This was discovered after compound 3 was prepared, and so phosphonate 31 was not used for the synthesis of compound 3. In any case, we preferred methyl-protecting groups as opposed to ethyl-protecting groups for phosphonate protection since methyl groups are removed more readily by TMSBr than ethyl groups; this reduces the compounds exposure to TMSBr which can cause side reactions and lower yields. We would have preferred methyl protection for the synthesis of compound 4; however, this was not practical.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.