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Volumn 8, Issue 8, 2006, Pages 1533-1535

Total synthesis of ent-dihydrocorynantheol by using a proline-catalyzed asymmetric addition reaction

Author keywords

[No Author keywords available]

Indexed keywords

ALKALOID; DIHYDROCORYNANTHEOL; PROLINE;

EID: 33646448408     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol0530575     Document Type: Article
Times cited : (124)

References (34)
  • 14
    • 0004125379 scopus 로고    scopus 로고
    • Harwood Academic Publishers: Amsterdam, The Netherlands
    • (b) Rahman, A.-u.; Basha, A. Indole Alkaloids; Harwood Academic Publishers: Amsterdam, The Netherlands, 1998.
    • (1998) Indole Alkaloids
    • Rahman, A.-U.1    Basha, A.2
  • 15
    • 4243241249 scopus 로고
    • and references therein
    • Cox, E.; Cook, J. M. Chem. Rev. 1995, 95, 1797 and references therein.
    • (1995) Chem. Rev. , vol.95 , pp. 1797
    • Cox, E.1    Cook, J.M.2
  • 21
    • 33646450725 scopus 로고    scopus 로고
    • note
    • The relative configuration of 2 was determined by using the NOE analysis (see the Supporting Information). The absolute configuration was speculated according to those of the other addition products.
  • 33
    • 0037119742 scopus 로고    scopus 로고
    • Since the present reaction was slow, the excess amount of the enone was necessary for the progress of the reaction in tolerable time. The self-reaction of enones in the presence of proline catalyst was not observed in the present reaction; see: Ramachary, D. B.; Chowdari, N. S.; Barbas, C. F., III Tetrahedron Lett. 2002, 43, 6743.
    • (2002) Tetrahedron Lett. , vol.43 , pp. 6743
    • Ramachary, D.B.1    Chowdari, N.S.2    Barbas III, C.F.3
  • 34
    • 33646437883 scopus 로고    scopus 로고
    • note
    • 3CN, DMF, and THF were used for the reaction, the results were inferior to that of the DMSO solvent.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.