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Volumn 10, Issue 1, 2012, Pages 162-170

Rapid synthesis of highly functionalised α-amino amides and medium ring lactones using multicomponent reactions of amino alcohols and isocyanides

Author keywords

[No Author keywords available]

Indexed keywords

AMINO ALCOHOLS; CONVENTIONAL HEATING; DIASTEREO-SELECTIVITY; ISOCYANIDES; L-PROLINOL; MEDIUM RINGS; MULTI-COMPONENT REACTIONS; MULTICOMPONENTS; RAPID SYNTHESIS; REACTION CONDITIONS; THIOETHERS; THREE COMPONENT REACTIONS;

EID: 82955240823     PISSN: 14770520     EISSN: None     Source Type: Journal    
DOI: 10.1039/c1ob06534c     Document Type: Article
Times cited : (19)

References (44)
  • 27
    • 0000518943 scopus 로고
    • For previous examples of the use of acid-aldehydes in Ugi-like reactions, see
    • H. L. Wehrmeister J. Org. Chem. 1963 28 2587 2588
    • (1963) J. Org. Chem. , vol.28 , pp. 2587-2588
    • Wehrmeister, H.L.1
  • 44
    • 0030603133 scopus 로고    scopus 로고
    • The stereochemistry at the newly created chiral centre (*) was not determined An enhancement of the methine signal on the pyrrolidine ring was observed upon irradition of the benzylic methine proton for the (S,S) isomer. No such enhancement was observed for the (S,R) isomer. The nOe difference spectra are provided in the supporting information Microwave reactions were performed using a CEM Explorer microwave with an external IR temperature sensor (150 W power)
    • I. Ugi A. Demharter W. Hörl T. Schmid Tetrahedron 1996 52 11657 11664
    • (1996) Tetrahedron , vol.52 , pp. 11657-11664
    • Ugi, I.1    Demharter, A.2    Hörl, W.3    Schmid, T.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.