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Volumn , Issue 21, 2000, Pages 3603-3609

Synthesis of sugar-modified analogs of bredinin (mizoribine), a clinically useful immunosuppressant, by a novel photochemical imidazole ring-cleavage reaction as the key step

Author keywords

[No Author keywords available]

Indexed keywords

HYDROGENATION; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; PHOTOCHEMICAL REACTIONS; SUGAR (SUCROSE); SYNTHESIS (CHEMICAL);

EID: 0034619657     PISSN: 14704358     EISSN: None     Source Type: Journal    
DOI: 10.1039/b005510g     Document Type: Article
Times cited : (14)

References (24)
  • 1
    • 0034641451 scopus 로고    scopus 로고
    • This report constitutes Part 202 of our series Nucleosides and Nucleotides. Part 201: T. Umino, N. Minakawa and A. Matsuda, Tetrahedron Lett., 2000, 41, 6419.
    • (2000) Tetrahedron Lett. , vol.41 , pp. 6419
    • Umino, T.1    Minakawa, N.2    Matsuda, A.3
  • 20
    • 33645917892 scopus 로고    scopus 로고
    • unpublished results
    • H. Watababe, unpublished results: when bredinin was subjected to Yoshikawa's procedure, dehydration of the 4-carbamoyl moiety occurred, giving the corresponding 4-cyano derivative as the major product.
    • Watababe, H.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.