메뉴 건너뛰기




Volumn 57, Issue 12, 2002, Pages 2345-2355

Chemistry of renieramycins. Part 2.1 Partial reduction and nucleophilic substitution of hexahydro-1,5-imino-4-oxo-3-benzazocine-7,10-dione: Promising method to construct renieramycin J from renieramycin G via renieramycin E

Author keywords

[No Author keywords available]

Indexed keywords

BENZAZOCINE DERIVATIVE; HEXAHYDRO 1,5 IMINO 4 OXO 3 BENZAZOCINE 7,10 DIONE; NATURAL PRODUCT; RENIERAMYCIN E; RENIERAMYCIN G; RENIERAMYCIN J; UNCLASSIFIED DRUG;

EID: 0036901056     PISSN: 03855414     EISSN: None     Source Type: Journal    
DOI: 10.3987/com-02-9625     Document Type: Article
Times cited : (18)

References (29)
  • 3
    • 0024818627 scopus 로고
    • H. He and D. J. Faulkner, J. Org. Chem., 1989, 54, 5822; J. M. Frincke and D. J. Faulkner, J. Am. Chem. Soc., 1982, 104, 265.
    • (1989) J. Org. Chem. , vol.54 , pp. 5822
    • He, H.1    Faulkner, D.J.2
  • 6
    • 0012007238 scopus 로고    scopus 로고
    • note
    • For simplicity, IUPAC numbering of renieramycins is used in this paper, except in the EXPERIMENTAL.
  • 18
    • 0036300526 scopus 로고    scopus 로고
    • f) K. Suwanborirux, K. Charupant, S. Amnuoypol, S. Pummangura, A. Kubo, and N. Saito, J. Nat. Prod., 2002, 65, 935. Silver tetrafluoroborate has also been used for this type of conversion: see P. Magnus, L. Gazzard, L. Hobson, A. H. Payne, T. J. Rainey, N. Westlund, and V. Lyuch, Tetrahedron, 2002, 58, 3423.
    • (2002) J. Nat. Prod. , vol.65 , pp. 935
    • Suwanborirux, K.1    Charupant, K.2    Amnuoypol, S.3    Pummangura, S.4    Kubo, A.5    Saito, N.6
  • 19
    • 0037156634 scopus 로고    scopus 로고
    • f) K. Suwanborirux, K. Charupant, S. Amnuoypol, S. Pummangura, A. Kubo, and N. Saito, J. Nat. Prod., 2002, 65, 935. Silver tetrafluoroborate has also been used for this type of conversion: see P. Magnus, L. Gazzard, L. Hobson, A. H. Payne, T. J. Rainey, N. Westlund, and V. Lyuch, Tetrahedron, 2002, 58, 3423.
    • (2002) Tetrahedron , vol.58 , pp. 3423
    • Magnus, P.1    Gazzard, L.2    Hobson, L.3    Payne, A.H.4    Rainey, T.J.5    Westlund, N.6    Lyuch, V.7
  • 20
    • 0011969119 scopus 로고    scopus 로고
    • note
    • Cyclic aminal (5b) was easily converted into lactam (2b) using the basic workup in 80-90% yield (see EXPERIMENTAL).
  • 27
    • 0000029575 scopus 로고
    • ed. by A. J. C. Wilson, Kluwer Academic Publishers, Boston, Table 4.2.6.8
    • e) D. C. Creagh and W. J. McAuley, in International Tables for Crystallography, Vol. C, ed. by A. J. C. Wilson, Kluwer Academic Publishers, Boston, Table 4.2.6.8, 1992, pp. 219-222.
    • (1992) International Tables for Crystallography , vol.C , pp. 219-222
    • Creagh, D.C.1    McAuley, W.J.2
  • 28
    • 0000191360 scopus 로고
    • ed. by A. J. C. Wilson, Kluwer Academic Publishers, Boston, Table 4.2.4.3
    • f) D. C. Creagh and J. H. Hubble, in International Tables for Crystallography, Vol. C, ed. by A. J. C. Wilson, Kluwer Academic Publishers, Boston, Table 4.2.4.3, 1992, pp. 200-206.
    • (1992) International Tables for Crystallography , vol.C , pp. 200-206
    • Creagh, D.C.1    Hubble, J.H.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.