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Volumn 37, Issue 39, 1996, Pages 7001-7004

The first total synthesis of 15-epi-annonin I

Author keywords

[No Author keywords available]

Indexed keywords

ACETOGENIN; ANNONIN I; UNCLASSIFIED DRUG;

EID: 0039736637     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/0040-4039(96)01589-4     Document Type: Article
Times cited : (22)

References (29)
  • 4
    • 0029592717 scopus 로고
    • and references cited therein
    • b) Hoppe, R.; Scharf, H.-D. Synthesis 1995, 1447-1464 and references cited therein.
    • (1995) Synthesis , pp. 1447-1464
    • Hoppe, R.1    Scharf, H.-D.2
  • 7
    • 0001439593 scopus 로고
    • Annonaceous Acetogenins: Potent Mitochondrial Inhibitors with Diverse Applications
    • Arnason, J.T.; Mata, R.; Romeo, J.T. Eds.; Plenum Press: New York
    • 4. Gu, Z.M.; Zhao, G.-X.; Oberlies, N.H.; Zeng, L.; McLaughlin, J.L.: Annonaceous Acetogenins: Potent Mitochondrial Inhibitors with Diverse Applications. In Recent Advances in Phytochemistry; Arnason, J.T.; Mata, R.; Romeo, J.T. Eds.; Plenum Press: New York, 1995, Vol. 29, pp. 249-310.
    • (1995) Recent Advances in Phytochemistry , vol.29 , pp. 249-310
    • Gu, Z.M.1    Zhao, G.-X.2    Oberlies, N.H.3    Zeng, L.4    McLaughlin, J.L.5
  • 11
    • 0028870226 scopus 로고
    • b) The absolute configuration of 1a was determined by X-ray analysis of a derivative (see ref. 6a) in combination with comparative CD-spectroscopy of 1a and a reference butenolide: Gypser, A.; Büllow, C.; Scharf, H.-D. Tetrahedron 1995, 51, 1921-1930.
    • (1995) Tetrahedron , vol.51 , pp. 1921-1930
    • Gypser, A.1    Büllow, C.2    Scharf, H.-D.3
  • 27
    • 0025015338 scopus 로고
    • and protection as its t-butyldiphenylsilyl (TBDPS) ether
    • 14. Compound 8 was prepared by kinetic resolution of the corresponding γ-chloro allylic alcohol, subsequent dehydrohalogenation (Ito, T.; Okamoto, S.; Sato, F. Tetrahedron Lett. 1990, 31, 6399-6402) and protection as its t-butyldiphenylsilyl (TBDPS) ether.
    • (1990) Tetrahedron Lett. , vol.31 , pp. 6399-6402
    • Ito, T.1    Okamoto, S.2    Sato, F.3
  • 28
    • 85030274917 scopus 로고    scopus 로고
    • note
    • 15. Compound 12 was prepared from 11-iodo-undecyne and (4S)-methyl-2-(phenylthio)-γ-butyrolactone similar to the procedure reported in ref. 9a.
  • 29
    • 85030272777 scopus 로고    scopus 로고
    • note
    • 3): δ = 14.10, 19.24, 22.08, 22.64, 24.45, 24.60, 25.20, 25.66, 26.09, 27.43, 28.79, 28.81, 29.21. 29.33, 29.38, 29.53, 29.57, 29.60, 29.61, 29.62, 29.69, 31.87, 32.42 (2C), 37.34, 37.52, 71.23 (2C), 71.87, 77.45, 82.76, 82.82, 83.06, 83.09, 134.43, 148.92, 173.92.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.