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Volumn 33, Issue 5, 2004, Pages 516-517

A modified thermodynamically controlled deracemization of 2-allylcyclohexanone and its application to asymmetric synthesis of (R)-(-)-epilachnene

Author keywords

[No Author keywords available]

Indexed keywords

CYCLOHEXANONE DERIVATIVE;

EID: 3242810489     PISSN: 03667022     EISSN: None     Source Type: Journal    
DOI: 10.1246/cl.2004.516     Document Type: Article
Times cited : (10)

References (16)
  • 5
    • 0345016361 scopus 로고    scopus 로고
    • Resolution efficiency (E, %) = yield(%) x enantiomeric excess(% ee) x 2/100. In the case of optical resolution, the value of E never exceed the 100%. See, K. Sakai, R. Sakurai, A. Yuzawa, and N. Hirayama, Tetrahedron: Asymmetry, 14, 3713 (2003).
    • (2003) Tetrahedron: Asymmetry , vol.14 , pp. 3713
    • Sakai, K.1    Sakurai, R.2    Yuzawa, A.3    Hirayama, N.4
  • 7
    • 3242783679 scopus 로고    scopus 로고
    • note
    • In a small-scale reaction, the yield of recovered (R)-2b was determined by GC on a Shimadzu GC-15A instrument using a J&W Scientific DB-1 capillary column. Dodecane was employed as an internal standard. The enantiomeric excess of the ketone was determined by GC using a chiral column (SUPELCO, α-DEX120).
  • 8
    • 0029967484 scopus 로고    scopus 로고
    • T. Tsunoda, C. Nagino, M. Oguri, and S. Itô, Tetrahedron Lett., 37, 2459 (1996); T. Tsunoda and S. Itô, J. Synth. Org. Chem. Jpn., 55, 631 (1997); S. Itô and T. Tsunoda, Pure Appl. Chem., 71, 1053 (1999); I. Sakamoto, H. Kaku, and T. Tsunoda, Chem. Pharm. Bull., 51, 474 (2003).
    • (1996) Tetrahedron Lett. , vol.37 , pp. 2459
    • Tsunoda, T.1    Nagino, C.2    Oguri, M.3    Itô, S.4
  • 9
    • 19044378999 scopus 로고    scopus 로고
    • T. Tsunoda, C. Nagino, M. Oguri, and S. Itô, Tetrahedron Lett., 37, 2459 (1996); T. Tsunoda and S. Itô, J. Synth. Org. Chem. Jpn., 55, 631 (1997); S. Itô and T. Tsunoda, Pure Appl. Chem., 71, 1053 (1999); I. Sakamoto, H. Kaku, and T. Tsunoda, Chem. Pharm. Bull., 51, 474 (2003).
    • (1997) J. Synth. Org. Chem. Jpn. , vol.55 , pp. 631
    • Tsunoda, T.1    Itô, S.2
  • 10
    • 18844421637 scopus 로고    scopus 로고
    • T. Tsunoda, C. Nagino, M. Oguri, and S. Itô, Tetrahedron Lett., 37, 2459 (1996); T. Tsunoda and S. Itô, J. Synth. Org. Chem. Jpn., 55, 631 (1997); S. Itô and T. Tsunoda, Pure Appl. Chem., 71, 1053 (1999); I. Sakamoto, H. Kaku, and T. Tsunoda, Chem. Pharm. Bull., 51, 474 (2003).
    • (1999) Pure Appl. Chem. , vol.71 , pp. 1053
    • Itô, S.1    Tsunoda, T.2
  • 11
    • 0242380658 scopus 로고    scopus 로고
    • T. Tsunoda, C. Nagino, M. Oguri, and S. Itô, Tetrahedron Lett., 37, 2459 (1996); T. Tsunoda and S. Itô, J. Synth. Org. Chem. Jpn., 55, 631 (1997); S. Itô and T. Tsunoda, Pure Appl. Chem., 71, 1053 (1999); I. Sakamoto, H. Kaku, and T. Tsunoda, Chem. Pharm. Bull., 51, 474 (2003).
    • (2003) Chem. Pharm. Bull. , vol.51 , pp. 474
    • Sakamoto, I.1    Kaku, H.2    Tsunoda, T.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.