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Volumn 51, Issue 1, 2012, Pages 40-42

1,2-dicarbonyl compounds as pronucleophiles in organocatalytic asymmetric transformations

Author keywords

1,2 dicarbonyls; asymmetric catalysis; domino reactions; organocatalysis; pronucleophiles

Indexed keywords

1,2-DICARBONYLS; ASYMMETRIC CATALYSIS; DOMINO REACTIONS; ORGANOCATALYSIS; PRONUCLEOPHILES;

EID: 84855269930     PISSN: 14337851     EISSN: 15213773     Source Type: Journal    
DOI: 10.1002/anie.201106741     Document Type: Review
Times cited : (49)

References (30)
  • 16
    • 33845495393 scopus 로고    scopus 로고
    • For asymmetric aldolization with pyruvic aldehyde dimethyl acetal as a masked 1,2-dicarbonyl compound catalyzed by (S)-proline, see:, D. Enders, T. Gasperi, Chem. Commun. 2007, 88.
    • (2007) Chem. Commun. , pp. 88
    • Enders, D.1    Gasperi, T.2
  • 27
    • 53549083631 scopus 로고    scopus 로고
    • for a previous similar sequence using 2-hydroxy-1,4-naphthoquinone that can be regarded as a 1,2-diketone type pronucleophile, see:, M. Rueping, E. Sugiono, E. Merino, Angew. Chem. 2008, 120, 3089
    • (2008) Angew. Chem. , vol.120 , pp. 3089
    • Rueping, M.1    Sugiono, E.2    Merino, E.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.