메뉴 건너뛰기




Volumn 47, Issue 43, 2006, Pages 7545-7549

Thiophenol-mediated improvement of the Pictet-Spengler cyclization of N-tosyl-β-phenethylamines with aldehydes

Author keywords

[No Author keywords available]

Indexed keywords

ALDEHYDE DERIVATIVE; LEWIS ACID; PHENETHYLAMINE DERIVATIVE; THIOPHENOL;

EID: 33748753336     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2006.08.097     Document Type: Article
Times cited : (8)

References (36)
  • 1
    • 0001625508 scopus 로고
    • The Pictet-Spengler Synthesis of Tetrahydroisoquinolines and Related Compounds
    • Adams R. (Ed), John Wiley and Sons, New York, USA
    • Whaley W.M., and Govindachari T.R. The Pictet-Spengler Synthesis of Tetrahydroisoquinolines and Related Compounds. In: Adams R. (Ed). Organic Reactions 6 (1951), John Wiley and Sons, New York, USA 151
    • (1951) Organic Reactions , vol.6 , pp. 151
    • Whaley, W.M.1    Govindachari, T.R.2
  • 4
    • 0000235287 scopus 로고
    • Katritzky A.R., and Rees C.W. (Eds), Pergamon, Oxford, UK
    • Jones G. In: Katritzky A.R., and Rees C.W. (Eds). Comprehensive Heterocyclic Chemistry Vol. 2 (1984), Pergamon, Oxford, UK 438-440
    • (1984) Comprehensive Heterocyclic Chemistry , vol.2 , pp. 438-440
    • Jones, G.1
  • 6
    • 27544453677 scopus 로고    scopus 로고
    • Synthesis of Optically-Active Isoquinoline and Indole Alkaloids Employing the Pictet-Spengler Condensation with Removable Chiral Auxiliaries Bound to Nitrogen
    • Vicario J.L. (Ed), Research SignPost, Trivandrum Chapter 4
    • Kaufman T.S. Synthesis of Optically-Active Isoquinoline and Indole Alkaloids Employing the Pictet-Spengler Condensation with Removable Chiral Auxiliaries Bound to Nitrogen. In: Vicario J.L. (Ed). New Methods for the Asymmetric Synthesis of Nitrogen Heterocycles (2005), Research SignPost, Trivandrum 99-147 Chapter 4
    • (2005) New Methods for the Asymmetric Synthesis of Nitrogen Heterocycles , pp. 99-147
    • Kaufman, T.S.1
  • 11
    • 0012566719 scopus 로고
    • Use of Carbonyl Derivatives for Heterocyclic Synthesis
    • Winterfeldt E. (Ed), Pergamon Press, Oxford, UK
    • Bringmann G., Ewers C.L.J., and Walter R. Use of Carbonyl Derivatives for Heterocyclic Synthesis. In: Winterfeldt E. (Ed). Comprehensive Organic Synthesis Vol. 6 (1991), Pergamon Press, Oxford, UK 736-740
    • (1991) Comprehensive Organic Synthesis , vol.6 , pp. 736-740
    • Bringmann, G.1    Ewers, C.L.J.2    Walter, R.3
  • 29
    • 33748746277 scopus 로고    scopus 로고
    • note
    • 4), concentrated under reduced pressure, and the residue was submitted to column chromatography.
  • 30
    • 33748746626 scopus 로고    scopus 로고
    • note
    • 4S requires C, 57.37; H, 4.81; N, 2.79.
  • 34
    • 0033978692 scopus 로고    scopus 로고
    • Thioacetals have been employed for the synthesis of tetrahydroisoquinoline derivatives, via thionium ions, see:
    • Thioacetals have been employed for the synthesis of tetrahydroisoquinoline derivatives, via thionium ions, see:. Padwa A., and Waterson A.G. J. Org. Chem. 65 (2000) 235
    • (2000) J. Org. Chem. , vol.65 , pp. 235
    • Padwa, A.1    Waterson, A.G.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.