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Volumn 30, Issue 15, 2011, Pages 4074-4086

N-heterocyclic pyridylmethylamines: Synthesis, complexation, molecular structure, and application to asymmetric Suzuki-Miyaura and oxidative coupling reactions

Author keywords

[No Author keywords available]

Indexed keywords

CATALYST ACTIVITY; CHELATION; LIGANDS; ORGANIC COMPOUNDS; SYNTHESIS (CHEMICAL);

EID: 79961089114     PISSN: 02767333     EISSN: 15206041     Source Type: Journal    
DOI: 10.1021/om200375s     Document Type: Article
Times cited : (40)

References (62)
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    • 0000718373 scopus 로고    scopus 로고
    • Pu, L. Chem. Rev. 1998, 98, 2405-2494
    • (1998) Chem. Rev. , vol.98 , pp. 2405-2494
    • Pu, L.1
  • 53
    • 0000690145 scopus 로고    scopus 로고
    • For vanadium catalysts in oxidative naphthol couplings see
    • For vanadium catalysts in oxidative naphthol couplings see: Barhate, N. B.; Chen, C.-T. Org. Lett. 2002, 4, 2529-2532
    • (2002) Org. Lett. , vol.4 , pp. 2529-2532
    • Barhate, N.B.1    Chen, C.-T.2
  • 57
    • 52049121580 scopus 로고    scopus 로고
    • For iron catalysts in oxidative naphthol couplings see:; J. Am. Chem. Soc. 2009, 6082-6083 For ruthenium catalysts in oxidative naphthol couplings see:;; Synlett 2000, 1433-1436 For electrochemical oxidative naphthol couplings see: J. Chem. Soc., Chem. Commun. 1994, 2535-2537
    • Takizawa, S.; Katayama, T.; Sasai, H. Chem. Commun. 2008, 4113-4122 For iron catalysts in oxidative naphthol couplings see: Egami, H.; Katsuki, T. J. Am. Chem. Soc. 2009, 131, 6082-6083 For ruthenium catalysts in oxidative naphthol couplings see: Irie, R.; Masutani, K.; Katsuki, T. Synlett 2000, 1433-1436 For electrochemical oxidative naphthol couplings see: Osa, T.; Kashiwagi, Y.; Yanagisawa, Y.; Bobbitt, J. M. J. Chem. Soc., Chem. Commun. 1994, 2535-2537
    • (2008) Chem. Commun. , vol.131 , pp. 4113-4122
    • Takizawa, S.1    Katayama, T.2    Sasai, H.3    Egami, H.4    Katsuki, T.5    Irie, R.6    Masutani, K.7    Katsuki, T.8    Osa, T.9    Kashiwagi, Y.10    Yanagisawa, Y.11    Bobbitt, J.M.12
  • 62
    • 4444337349 scopus 로고    scopus 로고
    • The absolute configuration of the binaphthyl product was determined as S by comparison with the literature; see
    • The absolute configuration of the binaphthyl product was determined as S by comparison with the literature; see: Kim, K. H.; Lee, D.-W.; Lee, Y.-S.; Ko, D.-H.; Ha, D.-C. Tetrahedron 2004, 60, 9037-9042
    • (2004) Tetrahedron , vol.60 , pp. 9037-9042
    • Kim, K.H.1    Lee, D.-W.2    Lee, Y.-S.3    Ko, D.-H.4    Ha, D.-C.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.