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Volumn 61, Issue 2, 1996, Pages 771-774

A new approach to the synthesis of piperazinomycin and bouvardin: Facile access to cycloisodityrosine via an intramolecular SNAr reaction

Author keywords

[No Author keywords available]

Indexed keywords

ANTIBIOTIC AGENT; BOUVARDIN; HEXAPEPTIDE; PIPERAZINOMYCIN; UNCLASSIFIED DRUG;

EID: 0030063925     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo951375j     Document Type: Article
Times cited : (57)

References (35)
  • 30
    • 0029047376 scopus 로고
    • Inoue et al. have recently detailed their total synthesis of deoxybouvardin: Inoue, T.; Inaba, T.; Umezawa, I.; Yuasa, M.; Itokawa, H.; Ogura, K.; Komatsu, K.; Hara, H.; Hoshino, O. Chem. Pharm. Bull. 1995, 43, 1325-1335. They noted that the 14-membered cycloisodityrosine, obtained via Yamamura's method, is an equilibrium mixture of two compounds. We think that these two separable compounds could be the two atropisomers instead of the two conformers as mentioned in ref 8.
    • (1995) Chem. Pharm. Bull. , vol.43 , pp. 1325-1335
    • Inoue, T.1    Inaba, T.2    Umezawa, I.3    Yuasa, M.4    Itokawa, H.5    Ogura, K.6    Komatsu, K.7    Hara, H.8    Hoshino, O.9


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.