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Volumn 11, Issue 22, 2013, Pages 3655-3663

Aqueous SDS micelle-promoted acid-catalyzed domino ABB′ imino Diels-Alder reaction: A mild and efficient synthesis of privileged 2-methyl-tetrahydroquinoline scaffolds

Author keywords

[No Author keywords available]

Indexed keywords

MICELLES; SCAFFOLDS;

EID: 84877738013     PISSN: 14770520     EISSN: None     Source Type: Journal    
DOI: 10.1039/c3ob40171e     Document Type: Article
Times cited : (25)

References (50)
  • 17
    • 0000252506 scopus 로고    scopus 로고
    • Catalysis of Diels-Alder Reactions in Water and in Hydrogen-Bonding Environments
    • ed. Z. Rappoport, John Wiley & Sons, Chichester, UK
    • A. Wittkopp and P. R. Schreiner, Catalysis of Diels-Alder Reactions in Water and in Hydrogen-Bonding Environments, in The Chemistry of Dienes and Polyenes, ed., Z. Rappoport, John Wiley & Sons, Chichester, UK, 2003, vol. 2, pp. 1029-1050
    • (2003) The Chemistry of Dienes and Polyenes , vol.2 , pp. 1029-1050
    • Wittkopp, A.1    Schreiner, P.R.2
  • 18
    • 0002287474 scopus 로고    scopus 로고
    • Water as Solvent in Organic Synthesis
    • ed. Knochel, Springer, Berlin, Heidelberg
    • A. Lubineau and J. Augé, Water as Solvent in Organic Synthesis, in Topics in Current Chemistry, ed., P. Knochel, Springer, Berlin, Heidelberg, 1999, vol. 206, pp. 2-33
    • (1999) Topics in Current Chemistry , vol.206 , pp. 2-33
    • Lubineau, A.1    Augé, J.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.