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Volumn 4, Issue 18, 2002, Pages 3147-3150

A Novel Metal Iodide Promoted Three-Component Synthesis of Substituted Pyrrolidines

Author keywords

[No Author keywords available]

Indexed keywords

ALDEHYDE; AMINE; CYCLOPROPANE DERIVATIVE; IODIDE; KETONE; MAGNESIUM; PYRROLIDINE DERIVATIVE;

EID: 0037026513     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol0264814     Document Type: Article
Times cited : (138)

References (31)
  • 1
    • 0442264990 scopus 로고    scopus 로고
    • note
    • A search on the pyrrolidine moiety in the MDDR (MACCS-II Drug Data Report) database gave over 11 000 hits. The database is available from MDL Information Systems Inc., San Leandro, CA 94577 and contains biologically active compounds in the early stages of drug development.
  • 9
    • 0442264989 scopus 로고    scopus 로고
    • U.S. Patent 5,707,798, 1998
    • Brann, M. R. U.S. Patent 5,707,798, 1998; Chem. Abstr. 1998, 128, 111548.
    • Brann, M.R.1
  • 10
    • 0007321318 scopus 로고    scopus 로고
    • Brann, M. R. U.S. Patent 5,707,798, 1998; Chem. Abstr. 1998, 128, 111548.
    • (1998) Chem. Abstr. , vol.128 , pp. 111548
  • 11
    • 84981754351 scopus 로고
    • (a) Biginelli, P. Ber. 1891, 24, 1317.
    • (1891) Ber. , vol.24 , pp. 1317
    • Biginelli, P.1
  • 17
    • 0035804418 scopus 로고    scopus 로고
    • For reviews on the use of cyclopropanes in organic synthesis
    • (a) Han, Z.; Uehira, S.; Tsuritani, T.; Shinokubo, H.; Oshima, K. Tetrahedron 2001, 57, 987. For reviews on the use of cyclopropanes in organic synthesis:
    • (2001) Tetrahedron , vol.57 , pp. 987
    • Han, Z.1    Uehira, S.2    Tsuritani, T.3    Shinokubo, H.4    Oshima, K.5
  • 22
    • 0442268050 scopus 로고    scopus 로고
    • note
    • 2 + MeOH 1%) or by PS-Isocyanate scavenger resin followed by an IEC, which afforded the pure compound in reasonable yield.
  • 27
    • 0442268048 scopus 로고    scopus 로고
    • a values for 4f and 4l were experimentally determined as 8.53 and 6.60, respectively
    • a values for 4f and 4l were experimentally determined as 8.53 and 6.60, respectively.
  • 28
    • 0442283586 scopus 로고
    • Lewis acids are known to promote the formation of imines, e.g.: (a) White, W. A.; Weingarten, H. J. Org. Chem. 1967, 32, 213. (b) Billmann, J. H.; Tai, K. M. J. Org. Chem. 1958, 23, 535. (c) Texier-Boullet, F. Synthesis 1985, 679.
    • (1967) J. Org. Chem. , vol.32 , pp. 213
    • White, W.A.1    Weingarten, H.2
  • 29
    • 33947462727 scopus 로고
    • Lewis acids are known to promote the formation of imines, e.g.: (a) White, W. A.; Weingarten, H. J. Org. Chem. 1967, 32, 213. (b) Billmann, J. H.; Tai, K. M. J. Org. Chem. 1958, 23, 535. (c) Texier-Boullet, F. Synthesis 1985, 679.
    • (1958) J. Org. Chem. , vol.23 , pp. 535
    • Billmann, J.H.1    Tai, K.M.2
  • 30
    • 85082932515 scopus 로고
    • Lewis acids are known to promote the formation of imines, e.g.: (a) White, W. A.; Weingarten, H. J. Org. Chem. 1967, 32, 213. (b) Billmann, J. H.; Tai, K. M. J. Org. Chem. 1958, 23, 535. (c) Texier-Boullet, F. Synthesis 1985, 679.
    • (1985) Synthesis , pp. 679
    • Texier-Boullet, F.1
  • 31
    • 0442264992 scopus 로고    scopus 로고
    • note
    • 2AlI protocol more useful when it comes to automation and library synthesis.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.