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Volumn 53, Issue 1, 1997, Pages 193-214

Synthesis of a 1,3,4,5-tetrahydrobenz[cd]indole via the vicarious nucleophilic substitution of hydrogen

Author keywords

[No Author keywords available]

Indexed keywords

INDOLE DERIVATIVE;

EID: 0342962077     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4020(96)00963-5     Document Type: Article
Times cited : (17)

References (41)
  • 29
    • 0343101336 scopus 로고    scopus 로고
    • Prolongation of the reaction time did not considerably change the ratio of 16 to 17
    • Prolongation of the reaction time did not considerably change the ratio of 16 to 17.
  • 34
    • 0343100982 scopus 로고    scopus 로고
    • 1H NMR spectra The diagnostic coupling constants C(1)H-C(2)H J=3.5 Hz and J=9.7 Hz were traced to trans 38a and cis 38b isomers respectively
    • 1H NMR spectra The diagnostic coupling constants C(1)H-C(2)H J=3.5 Hz and J=9.7 Hz were traced to trans 38a and cis 38b isomers respectively.
  • 41
    • 0342666626 scopus 로고    scopus 로고
    • This is the amount necessary to neutralize the remaining sulfuric acid and deprotonate the bromoketone plus 50% excess based on the starting bromohydrine
    • This is the amount necessary to neutralize the remaining sulfuric acid and deprotonate the bromoketone plus 50% excess based on the starting bromohydrine.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.