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Volumn 64, Issue 40, 2008, Pages 9408-9412

Felkin-Anh selectivity in Rh(bisoxazolinylphenyl)-catalyzed reductive aldol coupling reaction: asymmetric synthesis of stereotriads

Author keywords

Asymmetric catalysis; Bisoxazoline; Felkin Anh; Reductive aldol reaction; Rhodium

Indexed keywords

2 PHENYLPROPIONALDEHYDE; ACRYLIC ACID DERIVATIVE; PROPIONALDEHYDE; RHODIUM DERIVATIVE;

EID: 49349108145     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2008.07.092     Document Type: Article
Times cited : (26)

References (33)
  • 1
    • 34347225080 scopus 로고    scopus 로고
    • Metal Catalyzed Reductive C-C Bond Formation
    • Krische M.J. (Ed), Springer, Berlin, Heidelberg
    • Nishiyama H., and Shiomi T. Metal Catalyzed Reductive C-C Bond Formation. In: Krische M.J. (Ed). Topics in Current Chemistry Vol. 279 (2007), Springer, Berlin, Heidelberg 105
    • (2007) Topics in Current Chemistry , vol.279 , pp. 105
    • Nishiyama, H.1    Shiomi, T.2
  • 2
    • 34347230462 scopus 로고    scopus 로고
    • Metal Catalyzed Reductive C-C Bond Formation
    • Krische M.J. (Ed), Springer, Berlin, Heidelberg
    • Iida H., and Krische M.J. Metal Catalyzed Reductive C-C Bond Formation. In: Krische M.J. (Ed). Topics in Current Chemistry Vol. 279 (2007), Springer, Berlin, Heidelberg 77
    • (2007) Topics in Current Chemistry , vol.279 , pp. 77
    • Iida, H.1    Krische, M.J.2
  • 13
    • 49349108995 scopus 로고    scopus 로고
    • For example:
    • For example:
  • 20
    • 0028071378 scopus 로고
    • For diastereofacial selectivity of aldol reactions, see:
    • For diastereofacial selectivity of aldol reactions, see:. Paterson I., and Franklin A.S. Tetrahedron Lett. 35 (1994) 6925
    • (1994) Tetrahedron Lett. , vol.35 , pp. 6925
    • Paterson, I.1    Franklin, A.S.2
  • 24
    • 49349090900 scopus 로고    scopus 로고
    • For Felkin-Anh model:
    • For Felkin-Anh model:
  • 27
    • 49349106098 scopus 로고    scopus 로고
    • Also see:
    • Also see:
  • 29
    • 49249107741 scopus 로고    scopus 로고
    • John Wiley and Sons, Chichester, UK Chapter 21, p 429 and Chapter 30, p 681
    • Wyatt P., and Warren S. Organic Synthesis, Strategy and Control (2007), John Wiley and Sons, Chichester, UK Chapter 21, p 429 and Chapter 30, p 681
    • (2007) Organic Synthesis, Strategy and Control
    • Wyatt, P.1    Warren, S.2
  • 30
    • 49349101471 scopus 로고    scopus 로고
    • note
    • 2SiH, 75% yield with 5, 50:36:10:4 (major, 80% ee).
  • 31
    • 49349084215 scopus 로고    scopus 로고
    • note
    • When benzyl group was employed in place of isopropyl group of Rh(Phebox) 1b, the yield of 7 with (S)-5 was 72% with 84:5:8:3 diastereomer ratio and 99% ee for anti/syn.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.