메뉴 건너뛰기




Volumn 344, Issue 1, 2002, Pages 40-44

Threonine-Derived Phosphinite-Oxazoline Ligands for the Ir-Catalyzed Enantioselective Hydrogenation

Author keywords

Asymmetric catalysis; Hydrogenation; Iridium; Ligand design; N,P ligands

Indexed keywords


EID: 0002636574     PISSN: 16154150     EISSN: None     Source Type: Journal    
DOI: 10.1002/1615-4169(200201)344:1<40::AID-ADSC40>3.0.CO;2-7     Document Type: Article
Times cited : (161)

References (27)
  • 3
    • 0000681585 scopus 로고    scopus 로고
    • A. Lightfoot, P. Schnider, A. Pfaltz, Angew. Chem. 1998, 110, 3047-3050; Angew. Chem. Int. Ed. 1998,37, 2897-2899; D. G. Blackmond, A. Lightfoot, A. Pfaltz, T. Rosner, P. Schnider, N. Zimmermann, Chirality 2000, 12, 442-449.
    • (1998) Angew. Chem. , vol.110 , pp. 3047-3050
    • Lightfoot, A.1    Schnider, P.2    Pfaltz, A.3
  • 4
    • 0032476793 scopus 로고    scopus 로고
    • A. Lightfoot, P. Schnider, A. Pfaltz, Angew. Chem. 1998, 110, 3047-3050; Angew. Chem. Int. Ed. 1998,37, 2897-2899; D. G. Blackmond, A. Lightfoot, A. Pfaltz, T. Rosner, P. Schnider, N. Zimmermann, Chirality 2000, 12, 442-449.
    • (1998) Angew. Chem. Int. Ed. , vol.37 , pp. 2897-2899
  • 6
    • 0000361977 scopus 로고    scopus 로고
    • (Eds.: E. N. Jacobson, A. Pfaltz, H. Yamamoto), Springer, Berlin, Ch. 5.2
    • Review: R. L. Haltermann in Comprehensive Asymmetric Catalysis (Eds.: E. N. Jacobson, A. Pfaltz, H. Yamamoto), Springer, Berlin, 1999, Vol. 1, Ch. 5.2, p. 183-195; for titanocene and zirconocene catalysts, see: R. D. Broene, S. L. Buchwald, J. Am. Chem. Soc. 1993, 115, 12569-12570; M. V. Troutman, D. H. Appella, S. L. Buchwald, J. Am. Chem. Soc. 1999, 121, 4916-4917.
    • (1999) Comprehensive Asymmetric Catalysis , vol.1 , pp. 183-195
    • Haltermann, R.L.1
  • 7
    • 0027859051 scopus 로고
    • Review: R. L. Haltermann in Comprehensive Asymmetric Catalysis (Eds.: E. N. Jacobson, A. Pfaltz, H. Yamamoto), Springer, Berlin, 1999, Vol. 1, Ch. 5.2, p. 183-195; for titanocene and zirconocene catalysts, see: R. D. Broene, S. L. Buchwald, J. Am. Chem. Soc. 1993, 115, 12569-12570; M. V. Troutman, D. H. Appella, S. L. Buchwald, J. Am. Chem. Soc. 1999, 121, 4916-4917.
    • (1993) J. Am. Chem. Soc. , vol.115 , pp. 12569-12570
    • Broene, R.D.1    Buchwald, S.L.2
  • 8
    • 0033606284 scopus 로고    scopus 로고
    • Review: R. L. Haltermann in Comprehensive Asymmetric Catalysis (Eds.: E. N. Jacobson, A. Pfaltz, H. Yamamoto), Springer, Berlin, 1999, Vol. 1, Ch. 5.2, p. 183-195; for titanocene and zirconocene catalysts, see: R. D. Broene, S. L. Buchwald, J. Am. Chem. Soc. 1993, 115, 12569-12570; M. V. Troutman, D. H. Appella, S. L. Buchwald, J. Am. Chem. Soc. 1999, 121, 4916-4917.
    • (1999) J. Am. Chem. Soc. , vol.121 , pp. 4916-4917
    • Troutman, M.V.1    Appella, D.H.2    Buchwald, S.L.3
  • 9
  • 13
    • 0000280528 scopus 로고    scopus 로고
    • J. Blankenstein, A. Pfaltz, Angew. Chem. 2001, 113, 4577-4579; Angew. Chem. Int. Ed. 2001, 40, 4445-4447; J. Blankenstein, Dissertation, University of Basel, 2001.
    • (2001) Angew. Chem. , vol.113 , pp. 4577-4579
    • Blankenstein, J.1    Pfaltz, A.2
  • 14
    • 0035803746 scopus 로고    scopus 로고
    • J. Blankenstein, A. Pfaltz, Angew. Chem. 2001, 113, 4577-4579; Angew. Chem. Int. Ed. 2001, 40, 4445-4447; J. Blankenstein, Dissertation, University of Basel, 2001.
    • (2001) Angew. Chem. Int. Ed. , vol.40 , pp. 4445-4447
  • 15
    • 0346368068 scopus 로고    scopus 로고
    • Dissertation, University of Basel
    • J. Blankenstein, A. Pfaltz, Angew. Chem. 2001, 113, 4577-4579; Angew. Chem. Int. Ed. 2001, 40, 4445-4447; J. Blankenstein, Dissertation, University of Basel, 2001.
    • (2001)
    • Blankenstein, J.1
  • 16
    • 0035817233 scopus 로고    scopus 로고
    • 2 = H) have been recently applied in Pd-catalyzed allylic alkylation: G. Jones, C. J. Richards, Tetrahedron Lett. 2001, 42, 5553-5555.
    • (2001) Tetrahedron Lett. , vol.42 , pp. 5553-5555
    • Jones, G.1    Richards, C.J.2
  • 17
    • 0026604531 scopus 로고
    • P. Wipf, C. P. Miller, Tetrahedron Lett. 1992, 33, 907-910; review of Burgess reagent: C. Lambert, J. Prakt. Chem. 2000, 342, 518-522.
    • (1992) Tetrahedron Lett. , vol.33 , pp. 907-910
    • Wipf, P.1    Miller, C.P.2
  • 18
    • 0347874156 scopus 로고    scopus 로고
    • P. Wipf, C. P. Miller, Tetrahedron Lett. 1992, 33, 907-910; review of Burgess reagent: C. Lambert, J. Prakt. Chem. 2000, 342, 518-522.
    • (2000) J. Prakt. Chem. , vol.342 , pp. 518-522
    • Lambert, C.1
  • 20
    • 0345736903 scopus 로고    scopus 로고
    • note
    • 1 = Ph (CAS 82659-84-5) is commercially available from Aldrich (No.: 29,217-6).
  • 21
    • 0345736901 scopus 로고    scopus 로고
    • note
    • The relative configuration was confirmed by NOESY and ROESY NMR experiments [contact between C(4)-H and C(S)-H].
  • 26
    • 0000910778 scopus 로고
    • C. A. Willoughby, S. L. Buchwald, J. Am. Chem. Soc. 1994, 116, 8952-8965; C.A. Willoughby, S. L. Buchwald, J. Am. Chem. Soc. 1994, 116, 11703-11714.
    • (1994) J. Am. Chem. Soc. , vol.116 , pp. 8952-8965
    • Willoughby, C.A.1    Buchwald, S.L.2
  • 27
    • 3643128481 scopus 로고
    • C. A. Willoughby, S. L. Buchwald, J. Am. Chem. Soc. 1994, 116, 8952-8965; C.A. Willoughby, S. L. Buchwald, J. Am. Chem. Soc. 1994, 116, 11703-11714.
    • (1994) J. Am. Chem. Soc. , vol.116 , pp. 11703-11714
    • Willoughby, C.A.1    Buchwald, S.L.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.