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Volumn 1, Issue 4, 1999, Pages 623-625

Highly enantioselective catalytic conjugate additions to cyclohexadienones

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EID: 0001146718     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol990707u     Document Type: Article
Times cited : (115)

References (23)
  • 10
    • 0032503611 scopus 로고    scopus 로고
    • Highly enantioselective rhodium-catalyzed asymmetric 1,4-addition of aryl-and alkenylboronic acids to enones has been reported by Hayashi et al.: Takaya, Y.; Ogasawara, M.; Hayashi, T. J. Am. Chem. Soc. 1998, 120, 5579.
    • (1998) J. Am. Chem. Soc. , vol.120 , pp. 5579
    • Takaya, Y.1    Ogasawara, M.2    Hayashi, T.3
  • 12
    • 0003167637 scopus 로고
    • Rappoport, Z., Patai, S., Eds.; John Wiley: New York
    • Swenton, J. S. The chemistry of quinoid compounds; Rappoport, Z., Patai, S., Eds.; John Wiley: New York, 1988; Vol. 2, Part 2, p 899.
    • (1988) The Chemistry of Quinoid Compounds , vol.2 , Issue.2 PART , pp. 899
    • Swenton, J.S.1
  • 20
    • 0041572927 scopus 로고
    • Diastereoselective conjugate additions of trimethylaluminum to [(p-tolylsulfinyl)methyl]quinols have been reported: Pirrung M. C., Nunn D. S. Tetrahedron Lett. 1992, 33, 1992.
    • (1992) Tetrahedron Lett. , vol.33 , pp. 1992
    • Pirrung, M.C.1    Nunn, D.S.2
  • 23
    • 0041572926 scopus 로고    scopus 로고
    • note
    • A cis-directing effect of the methoxy substituent in the organoaluminum mediated conjugate addition of RLi and RMgBr to quinol ethers has been observed, see ref 8a.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.