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Volumn 18, Issue 8, 1999, Pages 1771-1787

Improved methods for the preparation of 2'-deoxyribonucleoside and ribonucleoside 3'-phosphoramidites with allylic protectors

Author keywords

[No Author keywords available]

Indexed keywords

3' PHOSPHORAMIDITE DERIVATIVE; DEOXYRIBONUCLEOSIDE; UNCLASSIFIED DRUG;

EID: 0032817033     PISSN: 07328311     EISSN: None     Source Type: Journal    
DOI: 10.1080/07328319908044842     Document Type: Article
Times cited : (14)

References (29)
  • 1
    • 0026606239 scopus 로고
    • and references cited therein
    • Beaucage, S. L.; Iyer, R. P. Tetrahedron 1992 48, 2223-2311, and references cited therein.
    • (1992) Tetrahedron , vol.48 , pp. 2223-2311
    • Beaucage, S.L.1    Iyer, R.P.2
  • 21
    • 85077634689 scopus 로고
    • and references cited therein
    • Mitsunobu, O. Synthesis 1981, 1-28, and references cited therein.
    • (1981) Synthesis , pp. 1-28
    • Mitsunobu, O.1
  • 23
    • 85038153181 scopus 로고    scopus 로고
    • note
    • In this reaction, even employing lower equivalents of tert-butylmagnesium chloride and AOC chloride did not give the N-mono-AOC derivative 13 or 15 as a major product.
  • 24
    • 85038154260 scopus 로고    scopus 로고
    • note
    • When a methanol solution was used in this reaction, cleavage of the desired allylic protecting groups took place to some extent.
  • 25
    • 85038168120 scopus 로고    scopus 로고
    • note
    • 2-allyloxycarbonylation for obtaining an acceptable yield.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.