메뉴 건너뛰기




Volumn 2, Issue 12, 2012, Pages 5147-5149

Total synthesis of batzelline C and isobatzelline C

Author keywords

[No Author keywords available]

Indexed keywords

FUNCTIONALIZATIONS; SYNTHESIS FEATURES; TOTAL SYNTHESIS;

EID: 84867058792     PISSN: None     EISSN: 20462069     Source Type: Journal    
DOI: 10.1039/c2ra20604h     Document Type: Article
Times cited : (17)

References (27)
  • 8
    • 0031017581 scopus 로고    scopus 로고
    • Iwao and co-workers reported a benzyne-mediated approach for makaluvamines using indole substrate and lithium isopropylcyclohexylamide. In this report, no cyclization-functionalization sequence was described
    • D. Roberts J. A. Joule J. Org. Chem. 1997 62 568
    • (1997) J. Org. Chem. , vol.62 , pp. 568
    • Roberts, D.1    Joule, J.A.2
  • 9
    • 0032581731 scopus 로고    scopus 로고
    • In the reported double functionalization of benzyne with a nitrogen nucleophile, a strong base such as s-BuLi 6b or intramolecular trapping 6c-6f of the generated anion species with an electrophile was utilized. Recently, Yoshida and co-workers reported on a three component reaction of benzyne, amine, and carbon dioxide to provide anthranilic acid. 6g
    • M. Iwao O. Motoi T. Fukuda F. Ishibashi Tetrahedron 1998 54 8999
    • (1998) Tetrahedron , vol.54 , pp. 8999
    • Iwao, M.1    Motoi, O.2    Fukuda, T.3    Ishibashi, F.4
  • 15
    • 61349134773 scopus 로고    scopus 로고
    • Recently, Garg and co-workers reported nucleophilic addition to indolyne and its application to synthesis of indolactam V
    • H. Yoshida T. Moroshita J. Ohshita Org. Lett. 2008 10 3845
    • (2008) Org. Lett. , vol.10 , pp. 3845
    • Yoshida, H.1    Moroshita, T.2    Ohshita, J.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.