메뉴 건너뛰기




Volumn 64, Issue 15, 1999, Pages 5504-5510

Conformational switching and the synthesis of spiro[2H-indol]-3(1H)-ones by radical cyclization

Author keywords

[No Author keywords available]

Indexed keywords

ANILINE DERIVATIVE; CYANIDE; CYCLOHEXANE DERIVATIVE; IMINE; KETONE; PIPERIDINE DERIVATIVE; SPIRO[2H INDOLE 2 CYCLOHEXAN] 3(1H) IMINE; SPIRO[2H INDOLE 2,4' PIPERIDIN] 3(1H) IMINE; UNCLASSIFIED DRUG;

EID: 0033597719     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo970105t     Document Type: Article
Times cited : (28)

References (20)
  • 2
    • 0030054277 scopus 로고    scopus 로고
    • For some recent work involving restricted conformations of piperidine systems and their application biological receptors, see: (a) Tong, W.; Collantes, E. R.; Chen, Y.; Welsh, W. J. J. Med. Chem. 1996, 39, 380. (b) Dijkstra, G. D. H. Recl. Trav. Chim. Pays-Bas 1993, 112, 151. (c) DiMeglio, C. M.; Froimowitz, M.; Makriyannis, A. Pharm. Res. 1993, 10, 1200. (d) McCague, R.; Rowlands, M. G. J. Med. Chem. 1992, 35, 3699 and references therein.
    • (1996) J. Med. Chem. , vol.39 , pp. 380
    • Tong, W.1    Collantes, E.R.2    Chen, Y.3    Welsh, W.J.4
  • 3
    • 0000545733 scopus 로고
    • For some recent work involving restricted conformations of piperidine systems and their application biological receptors, see: (a) Tong, W.; Collantes, E. R.; Chen, Y.; Welsh, W. J. J. Med. Chem. 1996, 39, 380. (b) Dijkstra, G. D. H. Recl. Trav. Chim. Pays-Bas 1993, 112, 151. (c) DiMeglio, C. M.; Froimowitz, M.; Makriyannis, A. Pharm. Res. 1993, 10, 1200. (d) McCague, R.; Rowlands, M. G. J. Med. Chem. 1992, 35, 3699 and references therein.
    • (1993) Recl. Trav. Chim. Pays-Bas , vol.112 , pp. 151
    • Dijkstra, G.D.H.1
  • 4
    • 0027160819 scopus 로고
    • For some recent work involving restricted conformations of piperidine systems and their application biological receptors, see: (a) Tong, W.; Collantes, E. R.; Chen, Y.; Welsh, W. J. J. Med. Chem. 1996, 39, 380. (b) Dijkstra, G. D. H. Recl. Trav. Chim. Pays-Bas 1993, 112, 151. (c) DiMeglio, C. M.; Froimowitz, M.; Makriyannis, A. Pharm. Res. 1993, 10, 1200. (d) McCague, R.; Rowlands, M. G. J. Med. Chem. 1992, 35, 3699 and references therein.
    • (1993) Pharm. Res. , vol.10 , pp. 1200
    • DiMeglio, C.M.1    Froimowitz, M.2    Makriyannis, A.3
  • 5
    • 0026765043 scopus 로고
    • and references therein
    • For some recent work involving restricted conformations of piperidine systems and their application biological receptors, see: (a) Tong, W.; Collantes, E. R.; Chen, Y.; Welsh, W. J. J. Med. Chem. 1996, 39, 380. (b) Dijkstra, G. D. H. Recl. Trav. Chim. Pays-Bas 1993, 112, 151. (c) DiMeglio, C. M.; Froimowitz, M.; Makriyannis, A. Pharm. Res. 1993, 10, 1200. (d) McCague, R.; Rowlands, M. G. J. Med. Chem. 1992, 35, 3699 and references therein.
    • (1992) J. Med. Chem. , vol.35 , pp. 3699
    • McCague, R.1    Rowlands, M.G.2
  • 17
    • 0344875769 scopus 로고    scopus 로고
    • Coordinates for the X-ray determinations have been deposited in the Cambridge Crystallographic Database and can be obtained upon request from the Director, Cambridge Crystallographic Data Centre, 12 Union Road, Cambridge, CB2 1EZ, U.K.
    • Coordinates for the X-ray determinations have been deposited in the Cambridge Crystallographic Database and can be obtained upon request from the Director, Cambridge Crystallographic Data Centre, 12 Union Road, Cambridge, CB2 1EZ, U.K.
  • 19
    • 0344012728 scopus 로고    scopus 로고
    • note
    • 3gem = 11.6 Hz.
  • 20
    • 0344012729 scopus 로고    scopus 로고
    • note
    • The 254-nm fluorescence of commonly used TLC plates makes the fluorescent imine difficult to see against the background.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.