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Volumn 2, Issue 8, 2000, Pages 1149-1152

Novel "reverse Kahne-type glycosylation": Access to O-, N-, and C-linked epipodophyllotoxin conjugates

Author keywords

[No Author keywords available]

Indexed keywords

CARBON; NITROGEN; OXYGEN; PODOPHYLLOTOXIN;

EID: 0034689853     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol005732a     Document Type: Article
Times cited : (20)

References (45)
  • 1
  • 18
    • 0026061989 scopus 로고
    • For an alternative glycosylation of (epi)podophyllotoxin, in which a glucosyl phosphinimidate or phosphate serves as glycosyl donor, see: Hashimoto, S.; Honda, T.; Ikegami, S. Tetrahedron Lett. 1991, 32, 1653-1654.
    • (1991) Tetrahedron Lett. , vol.32 , pp. 1653-1654
    • Hashimoto, S.1    Honda, T.2    Ikegami, S.3
  • 32
    • 0033953820 scopus 로고    scopus 로고
    • For both complementary mechanistic studies and the application of Kahne glycosylation chemistry to β-mannopyranosides, see: (a) Crich, D.; Li, H. J. Org. Chem. 2000, 65, 801-805.
    • (2000) J. Org. Chem. , vol.65 , pp. 801-805
    • Crich, D.1    Li, H.2
  • 38
    • 0043251510 scopus 로고    scopus 로고
    • note
    • N1-like transition state, all of the analogous, aglycon-based electrophiles are conceivable activated intermediates here.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.