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Volumn , Issue 7, 2003, Pages 971-974

Diels-Alder reactions of 4-alkoxy-4-alkylcyclohexa-2,5-dienimines: Synthesis of 5-alkylindoles

Author keywords

Diels Alder; Heterocycles; Indoles; Quinones

Indexed keywords

1,3 BUTADIENE DERIVATIVE; 4 ALKOXY 4 CYCLOHEXA 2,5 DIENIMINE; 5 INDOLE; ACID; DIHYDRONAPHTHALENE; IMINE; INDOLE DERIVATIVE; NAPHTHALENE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 0037562436     PISSN: 09365214     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (29)

References (23)
  • 9
    • 0038590212 scopus 로고
    • Kraus and co-workers cleaved a 1,4-tosylamido dihydronaphthalene in an elegant synthesis of the pyrroloindole subunit of CC-1065. See: Kraus, G. A.; Yue, S.; Sy, J. J. Org. Chem. 1985, 50, 284.
    • (1985) J. Org. Chem. , vol.50 , pp. 284
    • Kraus, G.A.1    Yue, S.2    Sy, J.3
  • 10
    • 0037576112 scopus 로고    scopus 로고
    • note
    • The Diels-Alder reactions of N-arylsulfonyl QIK's at ambient pressures and conversion to indoles have been studied by us will be reported in due course.
  • 20
    • 0038251718 scopus 로고    scopus 로고
    • note
    • 2S: found 327.1297, requires 327.1293.
  • 21
    • 0037576111 scopus 로고    scopus 로고
    • note
    • 3S: found 341.1089, requires 341.1086.
  • 22
    • 0037576110 scopus 로고    scopus 로고
    • Direct oxidative scission was unsuccessful
    • Direct oxidative scission was unsuccessful.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.