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Volumn 4, Issue 25, 2002, Pages 4515-4517

The Stereocontrolled Total Synthesis of (-)-O-Methylpallidinine

Author keywords

[No Author keywords available]

Indexed keywords

BRIDGED COMPOUND; MORPHINAN DERIVATIVE; O METHYLPALLIDININE; O-METHYLPALLIDININE;

EID: 0037069730     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol027040n     Document Type: Article
Times cited : (20)

References (17)
  • 2
    • 77957027656 scopus 로고
    • Brossi, A., Ed.; Academic Press: New York
    • For a pertinent review, see: Szantay, C.; Dørnyei, G. The Alkaloids; Brossi, A., Ed.; Academic Press: New York, 1994; Vol. 45, pp 127-232.
    • (1994) The Alkaloids , vol.45 , pp. 127-232
    • Szantay, C.1    Dørnyei, G.2
  • 6
    • 0442264522 scopus 로고
    • Racemic synthesis of O-methylpallidinine, see: (a) MacMurry, J. E.; Farina, V. Tetrahedron Lett. 1983, 24, 4653. (b) McMurry, J. E.; Farina, V.; Scott, W. J.; Davidson, A. H.; Summers, D. R.; Shenvi, D. R. J. Org. Chem. 1984, 49, 3803. Kano, S.; Yokomatsu, T.; Nemoto, H.; Shibuya, S. J. Am. Chem. Soc. 1986, 108, 6746.
    • (1983) Tetrahedron Lett. , vol.24 , pp. 4653
    • MacMurry, J.E.1    Farina, V.2
  • 7
    • 0021723653 scopus 로고
    • Racemic synthesis of O-methylpallidinine, see: (a) MacMurry, J. E.; Farina, V. Tetrahedron Lett. 1983, 24, 4653. (b) McMurry, J. E.; Farina, V.; Scott, W. J.; Davidson, A. H.; Summers, D. R.; Shenvi, D. R. J. Org. Chem. 1984, 49, 3803. Kano, S.; Yokomatsu, T.; Nemoto, H.; Shibuya, S. J. Am. Chem. Soc. 1986, 108, 6746.
    • (1984) J. Org. Chem. , vol.49 , pp. 3803
    • McMurry, J.E.1    Farina, V.2    Scott, W.J.3    Davidson, A.H.4    Summers, D.R.5    Shenvi, D.R.6
  • 8
    • 0022521055 scopus 로고
    • Racemic synthesis of O-methylpallidinine, see: (a) MacMurry, J. E.; Farina, V. Tetrahedron Lett. 1983, 24, 4653. (b) McMurry, J. E.; Farina, V.; Scott, W. J.; Davidson, A. H.; Summers, D. R.; Shenvi, D. R. J. Org. Chem. 1984, 49, 3803. Kano, S.; Yokomatsu, T.; Nemoto, H.; Shibuya, S. J. Am. Chem. Soc. 1986, 108, 6746.
    • (1986) J. Am. Chem. Soc. , vol.108 , pp. 6746
    • Kano, S.1    Yokomatsu, T.2    Nemoto, H.3    Shibuya, S.4
  • 14
    • 0036643978 scopus 로고    scopus 로고
    • (+)-ferruginol: ref 4
    • Utilization of the bicyclo[3.2.1]octenone chiral building block for natural product synthesis other than (-)-morphine, see: (a) (+)-ferruginol: ref 4. (b) Calcitriol CD-ring: ref 5. (+)-Vernolepin: Miyazawa, N.; Ogasawara, K. Synlett 2002, 125. 18-Ketoyohimbone: Miyazawa, N.; Ogasawara, K. Tetrahedron Lett. 1983, 43, 4773.
  • 15
    • 0036643978 scopus 로고    scopus 로고
    • Calcitriol CD-ring: ref 5
    • Utilization of the bicyclo[3.2.1]octenone chiral building block for natural product synthesis other than (-)-morphine, see: (a) (+)-ferruginol: ref 4. (b) Calcitriol CD-ring: ref 5. (+)-Vernolepin: Miyazawa, N.; Ogasawara, K. Synlett 2002, 125. 18-Ketoyohimbone: Miyazawa, N.; Ogasawara, K. Tetrahedron Lett. 1983, 43, 4773.
  • 16
    • 0442264515 scopus 로고    scopus 로고
    • Utilization of the bicyclo[3.2.1]octenone chiral building block for natural product synthesis other than (-)-morphine, see: (a) (+)-ferruginol: ref 4. (b) Calcitriol CD-ring: ref 5. (c) (+)-Vernolepin: Miyazawa, N.; Ogasawara, K. Synlett 2002, 125. 18-Ketoyohimbone: Miyazawa, N.; Ogasawara, K. Tetrahedron Lett. 1983, 43, 4773.
    • (2002) Synlett , pp. 125
    • Miyazawa, N.1    Ogasawara, K.2
  • 17
    • 0036643978 scopus 로고    scopus 로고
    • Utilization of the bicyclo[3.2.1]octenone chiral building block for natural product synthesis other than (-)-morphine, see: (a) (+)-ferruginol: ref 4. (b) Calcitriol CD-ring: ref 5. (+)-Vernolepin: Miyazawa, N.; Ogasawara, K. Synlett 2002, 125. (d) 18-Ketoyohimbone: Miyazawa, N.; Ogasawara, K. Tetrahedron Lett. 1983, 43, 4773.
    • (1983) Tetrahedron Lett. , vol.43 , pp. 4773
    • Miyazawa, N.1    Ogasawara, K.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.