메뉴 건너뛰기




Volumn 75, Issue 1, 2008, Pages 43-56

Synthesis of cycloalkanoindoles, the carba analogs of physostigmine

Author keywords

[No Author keywords available]

Indexed keywords


EID: 43649101049     PISSN: 03855414     EISSN: None     Source Type: Journal    
DOI: 10.3987/COM-07-11154     Document Type: Article
Times cited : (9)

References (19)
  • 11
    • 2942578050 scopus 로고    scopus 로고
    • Hexahydrocyclopenta[b]indole skeleton was synthetized with standard Fischer indole cyclization of cyclopentanone phenylhydrazone followed by catalytic hydrogenation
    • Hexahydrocyclopenta[b]indole skeleton was synthetized with standard Fischer indole cyclization of cyclopentanone phenylhydrazone followed by catalytic hydrogenation. Welmaker G.S., and Sabalski J.E. Tetrahedron Lett. 45 (2004) 4851
    • (2004) Tetrahedron Lett. , vol.45 , pp. 4851
    • Welmaker, G.S.1    Sabalski, J.E.2
  • 12
    • 0001703953 scopus 로고
    • The N-methyl derivative was prepared by photochemical cyclization of N-cyclopentenyl-N methylbenzenamine
    • The N-methyl derivative was prepared by photochemical cyclization of N-cyclopentenyl-N methylbenzenamine. Chapman O.L., and Eian G.L. J Am. Chem. Soc. 90 (1968) 5329
    • (1968) J Am. Chem. Soc. , vol.90 , pp. 5329
    • Chapman, O.L.1    Eian, G.L.2
  • 14
    • 43649097060 scopus 로고    scopus 로고
    • Aza-Claisen rearrangement is a thermal [3,3]sigmatrop rearrangement of N-allyl-N- arylamines. This rearrangement usually requires more forcing conditions than those required for the classical Claisen rearrangement. However, both protic acids and Lewis acids promote aromatic aza-Claisen rearrangement
    • Aza-Claisen rearrangement is a thermal [3,3]sigmatrop rearrangement of N-allyl-N- arylamines. This rearrangement usually requires more forcing conditions than those required for the classical Claisen rearrangement. However, both protic acids and Lewis acids promote aromatic aza-Claisen rearrangement. Castro A.M.M. Chem. Rev. 104 (2004) 29
    • (2004) Chem. Rev. , vol.104 , pp. 29
    • Castro, A.M.M.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.