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Volumn 48, Issue 46, 2007, Pages 8182-8184

A variation of the Pictet-Spengler reaction via a sequential reduction-cyclization reaction of N-acylcarbamates: synthesis of 1-substituted tetrahydroisoquinoline derivatives

Author keywords

[No Author keywords available]

Indexed keywords

8 OXO O METHYLBHARATAMINE; CARBAMIC ACID DERIVATIVE; ISOINDOLOISOQUINOLONE; LAUDANOSINE; TETRAHYDROISOQUINOLINE DERIVATIVE; UNCLASSIFIED DRUG; XYLOPININE;

EID: 35348838923     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2007.09.073     Document Type: Article
Times cited : (16)

References (28)
  • 12
    • 31944452587 scopus 로고    scopus 로고
    • For recent catalytic asymmetric Pictet-Spengler reactions:
    • For recent catalytic asymmetric Pictet-Spengler reactions:. Seayad J., Seayad A.M., and List B. J. Am. Chem. Soc. 128 (2006) 1086-1087
    • (2006) J. Am. Chem. Soc. , vol.128 , pp. 1086-1087
    • Seayad, J.1    Seayad, A.M.2    List, B.3
  • 26
    • 35348906410 scopus 로고    scopus 로고
    • note
    • 2, ethyl acetate/hexanes as eluent) or crystallization.
  • 27
    • 35348912826 scopus 로고    scopus 로고
    • note
    • 2, -78 °C, 1 h), the reaction of compound 9 yielded phenylacetaldehyde (60%) and phenethylcarbamic acid ethyl ester (10) (69%), implying that the reduction took place smoothly but that the cyclization was difficult.{A figure is presented}


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.