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Volumn 54, Issue 5-6, 1998, Pages 781-790

Asymmetric dihydroxylation of 1-acyloxy-2(E)-alkenylphosphonates with AD-mix reagents. Effects of 1-acyloxy functional groups on the asymmetric dihydroxylation

Author keywords

[No Author keywords available]

Indexed keywords

PHOSPHONIC ACID DERIVATIVE;

EID: 0032576829     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4020(97)10342-8     Document Type: Article
Times cited : (31)

References (35)
  • 10
    • 0030907801 scopus 로고    scopus 로고
    • (b) Very recently, Shibasaki and co-workers have shown that asymmetric hydrophosphonylation of cinnamaldehyde catalyzed with a chiral bimetalic alkoxide (LLB) proceeds in good enantioselectivity (84% ee): Sasai, H.; Bougauchi, M.; Arai, T.; Shibasaki, M. Tetrahedron Lett. 1997, 38, 2717.
    • (1997) Tetrahedron Lett. , vol.38 , pp. 2717
    • Sasai, H.1    Bougauchi, M.2    Arai, T.3    Shibasaki, M.4
  • 11
    • 0010702202 scopus 로고    scopus 로고
    • For kinetic resolution of chiral racemic olefins by AD reaction: (a) ref. 1a
    • 5. For kinetic resolution of chiral racemic olefins by AD reaction: (a) ref. 1a.
  • 17
    • 84984392889 scopus 로고
    • 7. Lu, X.; Zhu, J. Synthesis 1986, 563. Lohray has reported AD reaction of 1 giving 2 or ent-2, however, the details about the determination of the absolute configuration are not disclosed: Lohray, B. B.; Maji, D. K.; Nandanan, E. Indian J. Chem., Sect. B 1995, 34B, 1023.
    • (1986) Synthesis , pp. 563
    • Lu, X.1    Zhu, J.2
  • 18
    • 0001237634 scopus 로고
    • 7. Lu, X.; Zhu, J. Synthesis 1986, 563. Lohray has reported AD reaction of 1 giving 2 or ent-2, however, the details about the determination of the absolute configuration are not disclosed: Lohray, B. B.; Maji, D. K.; Nandanan, E. Indian J. Chem., Sect. B 1995, 34B, 1023.
    • (1995) Indian J. Chem., Sect. B , vol.34 B , pp. 1023
    • Lohray, B.B.1    Maji, D.K.2    Nandanan, E.3
  • 24
    • 0010662947 scopus 로고    scopus 로고
    • note
    • 11. Partial 1,2-or 1,3-O,O-migration of the acetyl group was observed; these migration products make it difficult to isolate the dihydroxylation products as a pure state.
  • 29
    • 0030795643 scopus 로고    scopus 로고
    • 14. For double diastereoselection in the Sharpless asymmetric dihydroxylation: Guzman-Perez, A.; Corey, E. J. Tetrahedron Lett. 1997, 38, 5941.
    • (1997) Tetrahedron Lett. , vol.38 , pp. 5941
    • Guzman-Perez, A.1    Corey, E.J.2
  • 33
    • 0010710281 scopus 로고    scopus 로고
    • Under the conditions, the concomitant de-acetylation takes place
    • 17. Under the conditions, the concomitant de-acetylation takes place.
  • 34
    • 0010711265 scopus 로고    scopus 로고
    • General experimental aspects are described in the preceding paper (ref.2)
    • 18. General experimental aspects are described in the preceding paper (ref.2).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.