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Volumn 7, Issue 20, 1997, Pages 2687-2690

Structural analogues of the michellamine anti-HIV agents. Importance of the tetrahydroisoquinoline rings for biological activity

Author keywords

[No Author keywords available]

Indexed keywords

ANTI HUMAN IMMUNODEFICIENCY VIRUS AGENT; MICHELLAMINE A; MICHELLAMINE B; MICHELLAMINE DERIVATIVE; TETRAHYDROISOQUINOLINE; UNCLASSIFIED DRUG;

EID: 0030668534     PISSN: 0960894X     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0960-894X(97)10057-9     Document Type: Article
Times cited : (23)

References (17)
  • 15
    • 0343487557 scopus 로고    scopus 로고
    • note
    • For the cross-coupling reaction between Inflates 8 and the aryl boronic acids to occur, it was necessary to carefully de-oxygenate the reaction solution by purging with nitrogen for 15 min.
  • 16
    • 0342617487 scopus 로고    scopus 로고
    • note
    • Aryl boronic acids A, B, C and F were purchased from Aldrich Chemical Company. The N-acetate of boronate C was hydrolyzed during the deprotection step in the syntheses of 10g-10i. Boronates D and E were prepared from the corresponding aryl bromides using standard chemistry.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.