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Volumn 136, Issue 22, 2014, Pages 7825-7828

Enantiospecific intramolecular heck reactions of secondary benzylic ethers

Author keywords

[No Author keywords available]

Indexed keywords

AROMATIC COMPOUNDS; OLEFINS;

EID: 84901913289     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/ja5026485     Document Type: Article
Times cited : (94)

References (43)
  • 4
    • 0042379984 scopus 로고    scopus 로고
    • Review of asymmetric Heck reactions in synthesis
    • Review of asymmetric Heck reactions in synthesis: Dounay, A. B.; Overman, L. E. Chem. Rev. 2003, 103, 2945-2964
    • (2003) Chem. Rev. , vol.103 , pp. 2945-2964
    • Dounay, A.B.1    Overman, L.E.2
  • 5
    • 73449103586 scopus 로고    scopus 로고
    • Review of industrial applications of the Heck reaction
    • Review of industrial applications of the Heck reaction: Torborg, C.; Beller, M. Adv. Synth. Catal. 2009, 351, 3027-3043
    • (2009) Adv. Synth. Catal. , vol.351 , pp. 3027-3043
    • Torborg, C.1    Beller, M.2
  • 6
    • 84894438898 scopus 로고    scopus 로고
    • For a recent discussion, see
    • For a recent discussion, see: Oestreich, M. Angew. Chem., Int. Ed. 2014, 53, 2282-2285
    • (2014) Angew. Chem., Int. Ed. , vol.53 , pp. 2282-2285
    • Oestreich, M.1
  • 27
    • 84887750453 scopus 로고    scopus 로고
    • For a lead reference of the complementary stereoconvergent strategy, see
    • For a lead reference of the complementary stereoconvergent strategy, see: Do, H.-Q.; Chandrashekar, E. R. R.; Fu, G. C. J. Am. Chem. Soc. 2013, 135, 16288-16291
    • (2013) J. Am. Chem. Soc. , vol.135 , pp. 16288-16291
    • Do, H.-Q.1    Chandrashekar, E.R.R.2    Fu, G.C.3
  • 28
    • 77952578899 scopus 로고    scopus 로고
    • Additional bases, ligands, and TESOTf as an additive were examined, but the only product observed was 3. For acceleration of nickel-catalyzed Heck reactions using TESOTf, see
    • Additional bases, ligands, and TESOTf as an additive were examined, but the only product observed was 3. For acceleration of nickel-catalyzed Heck reactions using TESOTf, see: Matsubara, R.; Jamison, T. F. J. Am. Chem. Soc. 2010, 132, 6880-6881
    • (2010) J. Am. Chem. Soc. , vol.132 , pp. 6880-6881
    • Matsubara, R.1    Jamison, T.F.2
  • 32
    • 84866495240 scopus 로고    scopus 로고
    • For a recent example of an intramolecular palladium-catalyzed alkyne insertion/Suzuki reaction of alkyl iodides and aryl boronic esters, see
    • For a recent example of an intramolecular palladium-catalyzed alkyne insertion/Suzuki reaction of alkyl iodides and aryl boronic esters, see: Monks, B. A.; Cook, S. P. J. Am. Chem. Soc. 2012, 134, 15297-15300
    • (2012) J. Am. Chem. Soc. , vol.134 , pp. 15297-15300
    • Monks, B.A.1    Cook, S.P.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.