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Volumn , Issue 10, 2006, Pages 1589-1591

Diastereoselective conjugate addition of cyanide to α,β- unsaturated oxazolidinones: Enantioselective synthesis of ent-pregabalin and baclofen

Author keywords

Conjugate addition; Cyanide; Oxazolidinone; Samarium

Indexed keywords

BACLOFEN; CYANIDE; OXAZOLIDINONE DERIVATIVE; PREGABALIN; SAMARIUM; SAMARIUM ISOPROPOXIDE; UNCLASSIFIED DRUG;

EID: 33745712063     PISSN: 09365214     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2006-941584     Document Type: Article
Times cited : (34)

References (30)
  • 1
    • 0000146934 scopus 로고
    • (a) Review of conjugate addition of cyanide: Nagata, W.; Nozaki, H. Org. React. 1977, 25, 255.
    • (1977) Org. React. , vol.25 , pp. 255
    • Nagata, W.1    Nozaki, H.2
  • 2
    • 0037449629 scopus 로고    scopus 로고
    • and references therein
    • (b) For cyanide group manipulations, see: North, M. Tetrahedron: Asymmetry 2003, 14, 147; and references therein.
    • (2003) Tetrahedron: Asymmetry , vol.14 , pp. 147
    • North, M.1
  • 3
    • 70350342932 scopus 로고    scopus 로고
    • Katritzky, A. R.; Taylor, R. J. K.; Cossy, J., Eds.; Elsevier Pergamon: Oxford, and references therein
    • (c) For a review of stereoselective conjugate addition, see: Armstrong, A.; Convine, N. J. In Comprehensive Organic Functional Group Transformations II, Vol. 1; Katritzky, A. R.; Taylor, R. J. K.; Cossy, J., Eds.; Elsevier Pergamon: Oxford, 2005, 287; and references therein.
    • (2005) Comprehensive Organic Functional Group Transformations II , vol.1 , pp. 287
    • Armstrong, A.1    Convine, N.J.2
  • 7
    • 0011982881 scopus 로고    scopus 로고
    • For selected diastereoselective approaches, see: (a) Dahuron, N.; Langlois, N. Synlett 1996, 51.
    • (1996) Synlett , pp. 51
    • Dahuron, N.1    Langlois, N.2
  • 14
    • 33745715551 scopus 로고    scopus 로고
    • note
    • 3: 242.1505; found: 242.1498.
  • 15
    • 33745687260 scopus 로고    scopus 로고
    • note
    • Details will be provided in a full account of this work. We thank Dr. A. J. P. White, Dept. of Chemistry, Imperial College London, for this structure determination.
  • 21
    • 33745715548 scopus 로고    scopus 로고
    • See also ref. 2a and 3
    • (f) See also ref. 2a and 3.
  • 22
    • 0034727937 scopus 로고    scopus 로고
    • For selected approaches to (R)-baclofen employing conjugate addition as the key step, see: (a) Corey, E. J.; Zhang, F.-Y. Org. Lett. 2000, 2, 4257.
    • (2000) Org. Lett. , vol.2 , pp. 4257
    • Corey, E.J.1    Zhang, F.-Y.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.