메뉴 건너뛰기




Volumn 51, Issue 20, 2010, Pages 2771-2773

Synthetic studies on azadirachtin: stereoselective construction of the ABCE ring system

Author keywords

[No Author keywords available]

Indexed keywords

ALDEHYDE; ALLYL COMPOUND; AZADIRACHTIN; BORANE DERIVATIVE; PALLADIUM;

EID: 77950595616     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2010.03.077     Document Type: Article
Times cited : (19)

References (25)
  • 12
    • 0001215915 scopus 로고
    • Trost B.M. (Ed), Blackwell Scientific Publications, Oxford
    • Hoffmann R.W. In: Trost B.M. (Ed). Stereocontrolled Organic Synthesis (1994), Blackwell Scientific Publications, Oxford 259-274
    • (1994) Stereocontrolled Organic Synthesis , pp. 259-274
    • Hoffmann, R.W.1
  • 14
    • 0000094579 scopus 로고
    • Allylboron Reagents
    • Stereoselective Synthesis. Ahlbecht H., Helmchean G., Arend M., and Herrmann R. (Eds), Georg Thieme, Stuttgart
    • Roush W.R. Allylboron Reagents. In: Ahlbecht H., Helmchean G., Arend M., and Herrmann R. (Eds). Stereoselective Synthesis. Methods in Organic Chemistry E21b (1995), Georg Thieme, Stuttgart 1410-1485
    • (1995) Methods in Organic Chemistry E21b , pp. 1410-1485
    • Roush, W.R.1
  • 18
    • 1542763298 scopus 로고
    • For a review on ring-closing metathesis, see:
    • For a review on ring-closing metathesis, see:. Grubbs R.H., Miller S.J., and Fu G.C. Acc. Chem. Res. 28 (1995) 446
    • (1995) Acc. Chem. Res. , vol.28 , pp. 446
    • Grubbs, R.H.1    Miller, S.J.2    Fu, G.C.3
  • 21
    • 0033515797 scopus 로고    scopus 로고
    • Low reactivity of enol triflates in epoxidation is reported:
    • Low reactivity of enol triflates in epoxidation is reported:. Evarts J.B., and Fuchs P.L. Tetrahedron Lett. 40 (1999) 2703
    • (1999) Tetrahedron Lett. , vol.40 , pp. 2703
    • Evarts, J.B.1    Fuchs, P.L.2
  • 22
    • 77950593620 scopus 로고    scopus 로고
    • note
    • Epimer 28a in which the isopropoxy group is oriented over the B ring exhibited poor reactivity probably because of the steric hindrance around the enol triflate moiety.{A figure is presented}
  • 23
    • 77950593965 scopus 로고    scopus 로고
    • note
    • The stereochemistry of allylborane 30 was determined by the NOE measurements.
  • 25
    • 67649654327 scopus 로고    scopus 로고
    • Alkenyl lithium 32 was prepared by treating (E)-1-methoxy-3-(tributylstannyl)-2-butene with butyllithium. For the synthesis of (E)-3-(tributylstannyl)-2-buten-1-ol, see:
    • Alkenyl lithium 32 was prepared by treating (E)-1-methoxy-3-(tributylstannyl)-2-butene with butyllithium. For the synthesis of (E)-3-(tributylstannyl)-2-buten-1-ol, see:. Yoshimura F., Sasaki M., Hattori I., Komatsu K., Sakai M., Tanino K., and Miyashita M. Chem. Eur. J. 15 (2009) 6626
    • (2009) Chem. Eur. J. , vol.15 , pp. 6626
    • Yoshimura, F.1    Sasaki, M.2    Hattori, I.3    Komatsu, K.4    Sakai, M.5    Tanino, K.6    Miyashita, M.7


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.