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Volumn 348, Issue 16-17, 2006, Pages 2457-2465

Enantioselective Diels-Alder reaction of α-Acyloxyacroleins catalyzed by chiral 1,1′-binaphthyl-2,2′-diammonium salts

Author keywords

acyloxyacrolein; 1,1 binaphthyl 2,2 diamine; Ammonium salts; Cycloaddition; Diels Alder reaction

Indexed keywords


EID: 33845274327     PISSN: 16154150     EISSN: 15213897     Source Type: Journal    
DOI: 10.1002/adsc.200600322     Document Type: Article
Times cited : (88)

References (41)
  • 10
    • 14944346768 scopus 로고    scopus 로고
    • MacMillan failed to activate methacrolein with a secondary ammonium salt: R. K. Kunz, D. W. C. MacMillan, J. Am. Chem. Soc. 2005, 127, 3240-3241.
    • (2005) J. Am. Chem. Soc. , vol.127 , pp. 3240-3241
    • Kunz, R.K.1    MacMillan, D.W.C.2
  • 31
    • 33845247467 scopus 로고    scopus 로고
    • note
    • The reaction conducted in the presence of water (100 mol%) gave similar results. When the reaction was carried out in the presence of more than 500 mol% of water, the solvent was partially frozen and the reactivity was decreased.
  • 32
    • 33845239119 scopus 로고    scopus 로고
    • note
    • 2, cyclopentadiene polymerized and the Diels-Alder adducts were obtained with low yield and enantioselectivity.
  • 33
    • 33845241624 scopus 로고    scopus 로고
    • note
    • [6a]


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.