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Volumn 11, Issue 15, 2009, Pages 3366-3369

Stereocontrolled synthesis of spirooxindoles through lewis acid-promoted [5 + 2]-annulation of chiral silyl alcohols

Author keywords

[No Author keywords available]

Indexed keywords

ACID; ALCOHOL DERIVATIVE; INDOLE DERIVATIVE; OXINDOLE; PALLADIUM; SPIRO COMPOUND;

EID: 68149110228     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol901202t     Document Type: Article
Times cited : (57)

References (34)
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    • Recent pharmaceuticals: (d) Shangary, S.; Wang, S. Annu. Rev. Pharmacol. Toxicol. 2009, 49, 223.
    • Recent pharmaceuticals: (d) Shangary, S.; Wang, S. Annu. Rev. Pharmacol. Toxicol. 2009, 49, 223.
  • 10
    • 68149088613 scopus 로고    scopus 로고
    • Recent pharmaceutial applications of oxaspirocylic oxindoles: Chafeev, M, Chowdhury, S, Fraser, R, Fu, J, Kamboj, R, Hou, D, Liu, S, Seid Bagherzadeh, M, Sviridov, S, Sun, S, Sun, J, Chakka, N, Hsieh, T, Raina, V. Use of spiro-oxindole compounds as therapeutic agents. WO 2008060789, May 22, 2008
    • Recent pharmaceutial applications of oxaspirocylic oxindoles: Chafeev, M.; Chowdhury, S.; Fraser, R.; Fu, J.; Kamboj, R.; Hou, D.; Liu, S. ; Seid Bagherzadeh, M.; Sviridov, S.; Sun, S. ; Sun, J. ; Chakka, N.; Hsieh, T.; Raina, V. Use of spiro-oxindole compounds as therapeutic agents. WO 2008060789, May 22, 2008.
  • 27
    • 68149104170 scopus 로고    scopus 로고
    • The calculated ground-state energy diffence is based on the RHF/ 3-21G (*) model of crystal structures cis-7a and trans-7a.
    • The calculated ground-state energy diffence is based on the RHF/ 3-21G (*) model of crystal structures cis-7a and trans-7a.
  • 29
    • 68149140539 scopus 로고    scopus 로고
    • The absolute configuration of annulation products was confirmed by X-ray structure analysis of 6b; see the Supporting Information.
    • The absolute configuration of annulation products was confirmed by X-ray structure analysis of 6b; see the Supporting Information.
  • 30
    • 0000095354 scopus 로고    scopus 로고
    • Panek, J. S.; Beresis, R.; Xu, F.; Y.; Yang, M. J. Org. Chem. 1991, 56, 7341.
    • Panek, J. S.; Beresis, R.; Xu, F.; Y.; Yang, M. J. Org. Chem. 1991, 56, 7341.
  • 31
    • 68149085761 scopus 로고    scopus 로고
    • The absolute configuration of the spirocyclic carbon of products 10a-h was confirmed by X-ray crystal structure analysis of 12.
    • The absolute configuration of the spirocyclic carbon of products 10a-h was confirmed by X-ray crystal structure analysis of 12.
  • 33
    • 68149088612 scopus 로고    scopus 로고
    • See the Supporting Information
    • See the Supporting Information.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.