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Volumn 18, Issue 43, 2012, Pages 13861-13870

Asymmetric total synthesis of (-)-stenine and 9a-epi-stenine

Author keywords

alkaloids; asymmetric synthesis; chiral auxiliary; natural products; stenine

Indexed keywords

ALKALOIDS; ASYMMETRIC SYNTHESIS; CHIRAL AUXILIARIES; NATURAL PRODUCTS; STENINE;

EID: 84867522054     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.201200376     Document Type: Article
Times cited : (23)

References (56)
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    • 77957072071 scopus 로고
    • (Ed: R. H. F. Manske), Academic Press, New York
    • M. Götz, O. E. Edwards, in The Alkaloids, Vol. 9 (Ed:, R. H. F. Manske,), Academic Press, New York, 1967, pp. 545-551
    • (1967) The Alkaloids , vol.9 , pp. 545-551
    • Götz, M.1    Edwards, O.E.2
  • 15
  • 24
    • 0028810543 scopus 로고
    • they have also reported the total synthesis of a related Stemona alkaloid, tuberotemonine, see
    • P. Wipf, Y. Kim, D. M. Goldstein, J. Am. Chem. Soc. 1995, 117, 11106-11112; they have also reported the total synthesis of a related Stemona alkaloid, tuberotemonine, see
    • (1995) J. Am. Chem. Soc. , vol.117 , pp. 11106-11112
    • Wipf, P.1    Kim, Y.2    Goldstein, D.M.3
  • 31
    • 84862958665 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2012, 51, 1024-1027.
    • (2012) Angew. Chem. Int. Ed. , vol.51 , pp. 1024-1027
  • 54
    • 84875273621 scopus 로고    scopus 로고
    • Although chiral 23 was a glassy powder, racemic 23 was crystalline and a minor isomer was separated by recrystallization (AcOEt). The relative stereochemistry of 23 was determined by using X-ray crystallographic analysis of racemic 23. CCDC-199947 contains the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via www.ccdc.cam.ac.uk/data-request/cif.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.