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Volumn 46, Issue 6, 2009, Pages 1154-1176

Access to indoles via Diels-Alder reactions of 2-vinylpyrroles with maleimides

Author keywords

[No Author keywords available]

Indexed keywords

1 (2 METHOXY 1 PHENYLETHYL)1H PYRROLE 2,5 DIONE; 2 (1 ETHOXYETHYL) N METHYL 1H PYRROLE; 2 (1 ETHOXYETHYL)PYRROLE; 2 (1 HEPTENYL) 1H PYRROLE; 2 (1 PROPENYL)1H PYRROLE; 2 (2 BUT 2 ENYL) 1H PYRROLE; 2 (2 BUT 2 ENYL)N METHYL 1H PYRROLE; 2 (2 METHYLVINYL)PYRROLE DERIVATIVE; 2 (2 PROPENYL)1H PYRROLE; 2 (2,5 DIOXO 1H PYRROL 1 YL) 2 PHENYLETHYL ACETATE; 2 (4 ETHYLPHENYL)3A ALPHA,4,5,8B ALPHA TETRAHYDRO 2H,6H PYRROLO[3,4 E]INDOLE 1,3 DIONE; 2 (4 ISOPROPYLPHENYL)3A ALPHA,4,5,8B ALPHA TETRAHYDRO 2H,6H PYRROLO[3,4 E]INDOLE 1,3 DIONE; 2 (4 METHOXYPHENYL) 6 METHYL 3A ALPHA,4,5,8B ALPHA TETRAHYDRO 2H,6H PYRROLO[3,4 E]INDOLE 1,3 DIONE; 2 (4 METHOXYPHENYL)3A ALPHA,4,5,8B ALPHA TETRAHYDRO 2H,6H PYRROLO[3,4 E]INDOLE 1,3 DIONE; 2 (4 PHENOXYPHENYL)3A ALPHA,4,5,8B ALPHA TETRAHYDRO 2H,6H PYRROLO[3,4 E]INDOLE 1,3 DIONE; 2 BENZYL 3A ALPHA,4,5,8B ALPHA TETRAHYDRO 2H,6H PYRROLO[3,4 E]INDOLE 1,3 DIONE; 2 DIMETHYLAMINO 3A ALPHA,4,5,8 B ALPHA TETRAHYDRO 2H,6H PYRROLO[3,4 E]INDOLE 1,3 DIONE; 2 DIMETHYLAMINO 6 METHYL 3A ALPHA,4,5,8B ALPHA TETRAHYDRO 2H,6H PYRROLO[3,4 E]INDOLE 1,3 DIONE; 2 ETHENYL 1H PYRROLE; 2 PHENYL 3A ALPHA,4,5,8B ALPHA TETRAHYDRO 2H,6H PYRROLO[3,4 E]INDOLE 1,3 DIONE; 2 VINYLPYRROLE DERIVATIVE; 6 METHYL 2 PHENYL 3A ALPHA,4,5,8B ALPHA TETRAHYDRO 2H,6H PYRROLO[3,4 E]INDOLE 1,3 DIONE; INDOLE DERIVATIVE; MALEIMIDE DERIVATIVE; N H 2 VINYLPYRROLE DERIVATIVE; N METHYL 2 (1 PROPENYL)1H PYRROLE; N METHYL 2 (2 PROPENYL)1H PYRROLE; PYRROLE DERIVATIVE; TETRAHYDROINDOLE DERIVATIVE; UNCLASSIFIED DRUG; UNINDEXED DRUG;

EID: 72249088182     PISSN: 0022152X     EISSN: None     Source Type: Journal    
DOI: 10.1002/jhet.198     Document Type: Article
Times cited : (25)

References (58)
  • 1
    • 72249122166 scopus 로고    scopus 로고
    • Sundberg, R. J. Indoles; Katritzky, A. R., Meth-Cohn, O., Rees, C. W., Eds.; Academic Press: San Diego, 1996
    • Sundberg, R. J. Indoles; Katritzky, A. R., Meth-Cohn, O., Rees, C. W., Eds.; Academic Press: San Diego, 1996.
  • 26
    • 13844314710 scopus 로고    scopus 로고
    • PCT Int Appl, WO Pat. 2003051883 A1 20030626 CAN 139:69289 AN 2003:491229 (2003); 23 examples
    • Kanai, F.; Murakata, C.; Tsujita, T.; Yamashita, Y.; Mizukami, T.; Akinaga, S. PCT Int Appl, WO Pat. 2003051883 A1 20030626 CAN 139:69289 AN 2003:491229 (2003); Chem Abstr 2003, 139, 69289 (23 examples).
    • (2003) Chem Abstr , vol.139 , pp. 69289
    • Kanai, F.1    Murakata, C.2    Tsujita, T.3    Yamashita, Y.4    Mizukami, T.5    Akinaga, S.6
  • 27
    • 72249107794 scopus 로고
    • Jpn. Pat. 3,178,880 (1993); Although this patent claims the method of Diels-Alder reactions of 2-vinylpyrroles to make 2-H and 3-H indoles, of the 88 examples given, only two products are 2-H indoles, both of which are 3-Me indoles and only one of which has an N-H
    • Nagai, T.; Myokan, I.; Takashi, F.; Nomura, Y.; Mizutani, M.; Hori, T. Jpn. Pat. 3,178,880 (1993); Chem Abstr 1994, 120, 106973. Although this patent claims the method of Diels-Alder reactions of 2-vinylpyrroles to make 2-H and 3-H indoles, of the 88 examples given, only two products are 2-H indoles, both of which are 3-Me indoles and only one of which has an N-H.
    • (1994) Chem Abstr , vol.120 , pp. 106973
    • Nagai, T.1    Myokan, I.2    Takashi, F.3    Nomura, Y.4    Mizutani, M.5    Hori, T.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.