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Volumn 79, Issue 3, 2014, Pages 831-845

C=N-containing azaarenes as activating groups in enantioselective catalysis

Author keywords

[No Author keywords available]

Indexed keywords

HETEROCYCLIC COMPOUND; NITROGEN;

EID: 84893846246     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo402414k     Document Type: Article
Times cited : (121)

References (158)
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    • For an early example of enantioselective CuH-catalyzed 1,4-reduction of electron-deficient alkenes, see: Appella, D. H.; Moritani, Y.; Shintani, R.; Ferreira, E. M.; Buchwald, S. L. J. Am. Chem. Soc. 1999, 121, 9473-9474
    • (1999) J. Am. Chem. Soc. , vol.121 , pp. 9473-9474
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  • 59
    • 0032503611 scopus 로고    scopus 로고
    • For the first catalytic enantioselective rhodium-catalyzed 1,4-addition of organoboron reagents, see
    • For the first catalytic enantioselective rhodium-catalyzed 1,4-addition of organoboron reagents, see: Takaya, Y.; Ogasawara, M.; Hayashi, T.; Sakai, M.; Miyaura, N. J. Am. Chem. Soc. 1998, 120, 5579-5580
    • (1998) J. Am. Chem. Soc. , vol.120 , pp. 5579-5580
    • Takaya, Y.1    Ogasawara, M.2    Hayashi, T.3    Sakai, M.4    Miyaura, N.5
  • 64
    • 0037243669 scopus 로고    scopus 로고
    • For a review of Rh-catalyzed carbon-carbon bond-forming reactions of organometallic compounds, see
    • For a review of Rh-catalyzed carbon-carbon bond-forming reactions of organometallic compounds, see: Fagnou, K.; Lautens, M. Chem. Rev. 2003, 103, 169-196
    • (2003) Chem. Rev. , vol.103 , pp. 169-196
    • Fagnou, K.1    Lautens, M.2
  • 69
    • 2942585558 scopus 로고    scopus 로고
    • For a review of 1-azallylic anions in heterocyclic chemistry, see
    • For a review of 1-azallylic anions in heterocyclic chemistry, see: Mangelinckx, S.; Giubellina, N.; De Kimpe, N. Chem. Rev. 2004, 104, 2353-2400
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  • 85
    • 77955688261 scopus 로고    scopus 로고
    • For a conceptually similar approach using nitrophenylacetonitriles as pronucleophiles, see
    • For a conceptually similar approach using nitrophenylacetonitriles as pronucleophiles, see: Cid, M. B. n.; Duce, S.; Morales, S.; Rodrigo, E.; Ruano, J. L. G. a. Org. Lett. 2010, 12, 3586-3589
    • (2010) Org. Lett. , vol.12 , pp. 3586-3589
    • Cid, M.B.N.1    Duce, S.2    Morales, S.3    Rodrigo, E.4    Ruano, J.L.G.A.5
  • 118
  • 129
    • 18244395541 scopus 로고    scopus 로고
    • For a review of the enantioselective rhodium-catalyzed hydroboration of alkenes, see
    • For a review of the enantioselective rhodium-catalyzed hydroboration of alkenes, see: Carroll, A.-M.; O'Sullivan, T. P.; Guiry, P. J. Adv. Synth. Catal. 2005, 347, 609-631
    • (2005) Adv. Synth. Catal. , vol.347 , pp. 609-631
    • Carroll, A.-M.1    O'Sullivan, T.P.2    Guiry, P.J.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.