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Volumn 77, Issue 8, 2012, Pages 4079-4086

Hydroxy-amide functionalized azolium salts for Cu-catalyzed asymmetric conjugate addition: Stereocontrol based on ligand structure and copper precatalyst

Author keywords

[No Author keywords available]

Indexed keywords

1 ,4-ADDITION; AMINO ALCOHOLS; ASYMMETRIC CONJUGATE ADDITION; AZOLIUM SALTS; CATALYTIC AMOUNTS; CATALYTIC SYSTEM; CHIRAL LIGAND; COUNTERIONS; CU SPECIES; ENANTIOPURE; ENANTIOSELECTIVE; FUNCTIONALIZED; LIGAND PRECURSORS; LIGAND STRUCTURE; PRECATALYSTS; STEREOCONTROL;

EID: 84860147801     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo300472r     Document Type: Article
Times cited : (39)

References (72)
  • 67
    • 80755186997 scopus 로고    scopus 로고
    • 10.1016/j.tet.2011.04.028
    • We previously reported the ligand design for dual enantioselective control by using β-amino alcohols and α-amino esters, which are derived from natural amino acids: Yoshimura, M.; Shibata, N.; Kawakami, M.; Sakaguchi, S. Tetrahedron 2011, 10.1016/j.tet.2011.04.028
    • (2011) Tetrahedron
    • Yoshimura, M.1    Shibata, N.2    Kawakami, M.3    Sakaguchi, S.4
  • 72
    • 84856303686 scopus 로고    scopus 로고
    • 2 combined with 1 may take place through the model B, where anionic acetylacetonate ligand coordinates to a Cu center
    • (2012) J. Am. Chem. Soc. , vol.134 , pp. 1490
    • Jung, B.1    Hoveyda, A.H.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.