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Volumn 65, Issue 20, 2000, Pages 6666-6669

An efficient synthesis of a new series of acyclonucleosides starting from β-amino alcohols

Author keywords

[No Author keywords available]

Indexed keywords

ACYCLIC NUCLEOSIDE; AMINOALCOHOL;

EID: 0034613145     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo000812d     Document Type: Article
Times cited : (9)

References (29)
  • 3
    • 0034007575 scopus 로고    scopus 로고
    • Shaeffer, H. J.; Beauchamp, L.; De Miranda, P.; Elion, G. B.; Bauer, D. J.; Collins, P. Nature 1978, 272, 583. For a review on the synthesis of acyclovir and related compounds, see: Gao, H.; Mitra, A. K. Synthesis 2000, 329.
    • (2000) Synthesis , pp. 329
    • Gao, H.1    Mitra, A.K.2
  • 21
    • 0342837954 scopus 로고    scopus 로고
    • note
    • When TBAF was added prior to trimethylsilylcyanide or azide, substrate 2a led quickly to a compound which resulted from a β-elimination.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.