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Volumn 13, Issue 5, 2011, Pages 932-935

Highly enantioselective Pd-catalyzed allylic alkylation of indoles using sulfur-MOP ligand

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EID: 79952160314     PISSN: 15237060     EISSN: 15237052     Source Type: Journal    
DOI: 10.1021/ol102977b     Document Type: Article
Times cited : (67)

References (37)
  • 1
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    • For some recent examples of chiral mixed phosphorus/sulfur ligands, see
    • For some recent examples of chiral mixed phosphorus/sulfur ligands, see: Oura, I.; Shimizu, K.; Ogata, K.; Fukuzawa, S.-i. Org. Lett. 2010, 12, 1752
    • (2010) Org. Lett. , vol.12 , pp. 1752
    • Oura, I.1    Shimizu, K.2    Ogata, K.3    Fukuzawa, S.-I.4
  • 9
    • 7444262096 scopus 로고    scopus 로고
    • Sulfur-MOP ligands containing alkyl sulfur substituents, see
    • Sulfur-MOP ligands containing alkyl sulfur substituents, see: Zhang, W.; Shi, M. Tetrahedron: Asymmetry 2004, 15, 3467
    • (2004) Tetrahedron: Asymmetry , vol.15 , pp. 3467
    • Zhang, W.1    Shi, M.2
  • 12
    • 77955673540 scopus 로고    scopus 로고
    • For some recent reviews of biologically active indoles and derivatives, see
    • For some recent reviews of biologically active indoles and derivatives, see: Kochanowska-Karamyan, A.; Hamann, M. T. Chem. Rev. 2010, 110, 4489
    • (2010) Chem. Rev. , vol.110 , pp. 4489
    • Kochanowska-Karamyan, A.1    Hamann, M.T.2
  • 16
    • 77953276740 scopus 로고    scopus 로고
    • For recent reviews of catalytic asymmetric Friedel-Crafts alkylations of indoles, see
    • For recent reviews of catalytic asymmetric Friedel-Crafts alkylations of indoles, see: Zeng, M.; You, S.-L. Synlett 2010, 1289
    • (2010) Synlett , pp. 1289
    • Zeng, M.1    You, S.-L.2
  • 27
    • 0042379988 scopus 로고    scopus 로고
    • For some reviews, see
    • For some reviews, see: Trost, B. M.; Crawley, M. L. Chem. Rev. 2003, 103, 2921
    • (2003) Chem. Rev. , vol.103 , pp. 2921
    • Trost, B.M.1    Crawley, M.L.2
  • 34
    • 0001036697 scopus 로고
    • Chan and co-workers also reported the significant effect of base on the enantioselectivity of Pd-catalyzed asymmetric allylic alkylations of indole. See ref 1g
    • Trost, B. M.; Bunt, R. C. J. Am. Chem. Soc. 1994, 116, 4089. Chan and co-workers also reported the significant effect of base on the enantioselectivity of Pd-catalyzed asymmetric allylic alkylations of indole. See ref 1g
    • (1994) J. Am. Chem. Soc. , vol.116 , pp. 4089
    • Trost, B.M.1    Bunt, R.C.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.