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Volumn 17, Issue 32, 2011, Pages 8780-8783

Highly active organocatalysts for asymmetric anti-mannich reactions

Author keywords

asymmetric catalysis; desymmetrization; mannich reactions; organocatalysis; ring opening

Indexed keywords

ASYMMETRIC CATALYSIS; DESYMMETRIZATION; MANNICH REACTIONS; ORGANOCATALYSIS; RING OPENING;

EID: 79960833697     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.201101513     Document Type: Article
Times cited : (43)

References (39)
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  • 9
    • 0037028550 scopus 로고    scopus 로고
    • For recent reviews on organocatalytic Mannich reactions, see
    • B. List, P. Pojarliev, W. T. Biller, H. J. Martin, J. Am. Chem. Soc. 2002, 124, 827-833; For recent reviews on organocatalytic Mannich reactions, see
    • (2002) J. Am. Chem. Soc. , vol.124 , pp. 827-833
    • List, B.1    Pojarliev, P.2    Biller, W.T.3    Martin, H.J.4
  • 14
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    • in (Eds: E. N. Jacobsen, A. Pfaltz, H. Yamamoto), Springer, New York, Chapter
    • E. N. Jacobsen, M. H. Wu, in Comprehensive Asymmetric Catalysis (Eds:, E. N. Jacobsen, A. Pfaltz, H. Yamamoto,), Springer, New York, 1999, Chapter 35.
    • (1999) Comprehensive Asymmetric Catalysis
    • Jacobsen, E.N.1    Wu, M.H.2
  • 39
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    • (ref. [6a]) reported a single case where the reaction of propanal with the PMP imine of ethyl glyoxylate was catalyzed by 0.2 mol% of an axially chiral aminosulfonamide; the reaction required 22 h at RT for completion
    • Maruoka et al. (ref. [6a]) reported a single case where the reaction of propanal with the PMP imine of ethyl glyoxylate was catalyzed by 0.2 mol% of an axially chiral aminosulfonamide; the reaction required 22 h at RT for completion.
    • Maruoka1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.