메뉴 건너뛰기




Volumn , Issue 8, 2007, Pages 1159-1168

Neutral yttrium tris(amide) and ate complexes coordinated by an (R)-N,N′-diisopropyl-1,1′-binaphthyl-2,2′-diamido ligand as enantioselective catalysts for intramolecular hydroamination

Author keywords

Asymmetric catalysis; Hydroamination; N ligands; Nitrogen heterocycles; Yttrium

Indexed keywords

CATALYSIS; CHELATION; CHLORINE COMPOUNDS; ENANTIOSELECTIVITY; LITHIUM COMPOUNDS; NITROGEN; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; X RAY ANALYSIS; YTTRIUM COMPOUNDS;

EID: 34250702600     PISSN: 14341948     EISSN: 10990682     Source Type: Journal    
DOI: 10.1002/ejic.200600872     Document Type: Article
Times cited : (55)

References (69)
  • 1
    • 0000788623 scopus 로고    scopus 로고
    • For general reviews on hydroamination reactions, see: a
    • For general reviews on hydroamination reactions, see: a) T. E. Müller, M. Beller, Chem. Rev. 1998, 98, 675-704;
    • (1998) Chem. Rev , vol.98 , pp. 675-704
    • Müller, T.E.1    Beller, M.2
  • 28
    • 0037715347 scopus 로고    scopus 로고
    • For reviews on enantioselective hydroamination reactions, see: a
    • For reviews on enantioselective hydroamination reactions, see: a) P. W. Roesky, T. E. Müller, Angew. Chem. Int. Ed. 2003, 42, 2708-2710;
    • (2003) Angew. Chem. Int. Ed , vol.42 , pp. 2708-2710
    • Roesky, P.W.1    Müller, T.E.2
  • 63
    • 85153271805 scopus 로고    scopus 로고
    • We have checked that the mono- and dilithium salts of the (R)-N,N′-diisopropyl-1,1′-binaphthyl-2,2′-diamido ligand are not active catalysts for the hydroamination reactions even at higher temperatures see ref.[4b
    • [4b]).
  • 65
    • 85153319965 scopus 로고    scopus 로고
    • SIR97, a program for automatic solution of crystal structures by direct methods: A. Altomare, M. C. Burla, M. Camalli, G. L. Cascarano, C. Giacovazzo, A. Guagliardi, A. G. G. Moliterni, G. Polidori, R. Spagn, J. Appl. Crystallogr. 1999, 32, 115.
    • SIR97, a program for automatic solution of crystal structures by direct methods: A. Altomare, M. C. Burla, M. Camalli, G. L. Cascarano, C. Giacovazzo, A. Guagliardi, A. G. G. Moliterni, G. Polidori, R. Spagn, J. Appl. Crystallogr. 1999, 32, 115.
  • 69
    • 85153210248 scopus 로고    scopus 로고
    • ORTEP3 for Windows: L. J. Farrugia, J. Appl. Crystallogr. 1997, 30, 565.
    • ORTEP3 for Windows: L. J. Farrugia, J. Appl. Crystallogr. 1997, 30, 565.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.