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Volumn 12, Issue 3, 2010, Pages 416-419

Unusual approach to branched 3-alkynylamides and to 1,5-dihydropyrrol-2- ones

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EID: 75749150832     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol902472r     Document Type: Article
Times cited : (41)

References (54)
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    • Stang, P. J., Diederich, F., Eds.; Wiley-VCH: Weinheim
    • (a) Modern Acetylene Chemistry; Stang, P. J., Diederich, F., Eds.; Wiley-VCH: Weinheim, 1995.
    • (1995) Modern Acetylene Chemistry
  • 18
    • 0036077326 scopus 로고    scopus 로고
    • (g) Zard, S. Z. Chem. Comm. 2002, 1555. For an application in the synthesis of odorant cycloalkynes, see:
    • (2002) Chem. Comm. , pp. 1555
    • Zard, S.Z.1
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    • 0000971565 scopus 로고
    • Katritzky, A. R., Rees, C. W., Eds.; Pergamon Press: Oxford
    • (a) Lang, S. A.; Lin, Y.-I. In Comprehensive Heterocyclic Chemistry; Katritzky, A. R., Rees, C. W., Eds.; Pergamon Press: Oxford, 1984; Vol.6, pp 103-105.
    • (1984) Comprehensive Heterocyclic Chemistry , vol.6 , pp. 103-105
    • Lang, S.A.1    Lin, Y.-I.2
  • 25
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    • For recent reviews on isocyanides in multicomponent reactions, see: (a) Dömling, A. Chem. Rev. 2006, 106, 17.
    • (2006) Chem. Rev. , vol.106 , pp. 17
    • Dömling, A.1
  • 33
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    • As one referee pointed out, it is possible that that iodination occurs first on the nitrogen of the amide to give the corresponding N-iodoamide, which in turn reacts with the alkyne
    • As one referee pointed out, it is possible that that iodination occurs first on the nitrogen of the amide to give the corresponding N-iodoamide, which in turn reacts with the alkyne.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.