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Volumn 46, Issue 36, 2005, Pages 6045-6047

Effect of solvent polarity on N-H insertion versus rearrangement of alkylidene carbenes

Author keywords

Carbene rearrangement; Diphenylacetylenes; Indoles; Intramolecular N H insertion; Solvent polarity

Indexed keywords

ACETYLENE; ALKYNE; BENZOPHENONE DERIVATIVE; CARBENOID; DIAZOMETHANE; ETHER; HYDROGEN; INDOLE; NITROGEN; SOLVENT; TRIMETHYLSILYLDIAZOMETHANE; UNCLASSIFIED DRUG;

EID: 23244445079     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2005.07.015     Document Type: Article
Times cited : (5)

References (18)
  • 3
    • 3242777629 scopus 로고    scopus 로고
    • A recent publication reports a similar mixture: T. Miyagi, Y. Hari, and T. Aoyama Tetrahedron Lett. 45 2004 6303 6305 Aoyama and co-workers observed that the N-tosyl derivative of 1 was cleanly converted to the N-tosyl derivative of 2 when treated with lithiated TMSDM in THF
    • (2004) Tetrahedron Lett. , vol.45 , pp. 6303-6305
    • Miyagi, T.1    Hari, Y.2    Aoyama, T.3
  • 4
    • 33544467007 scopus 로고    scopus 로고
    • note
    • 9
  • 16
    • 33544468720 scopus 로고    scopus 로고
    • note
    • The reaction of 2-amino-5-nitrobenzophenone 10 gave only 3-phenyl-5-nitroindole 11 in 70% yield under the reaction conditions outlined above.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.