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Volumn 72, Issue 17, 2007, Pages 6588-6590

A chelation-assisted transformation: Synthesis of maleimides by the Rh-catalyzed carbonylation of alkynes with pyridin-2-ylmethylamine

Author keywords

[No Author keywords available]

Indexed keywords

MALEIMIDE DERIVATIVES; PYRIDINE NITROGEN;

EID: 34547951150     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo071029p     Document Type: Article
Times cited : (31)

References (39)
  • 1
    • 0004100846 scopus 로고
    • For reviews on carbonylation reactions, see:, Falbe, J, Ed, Springer-Verlag: Berlin, Germany
    • For reviews on carbonylation reactions, see: Mullen, A. In New Syntheses with Carbon Monoxide; Falbe, J., Ed.; Springer-Verlag: Berlin, Germany, 1980; pp 242-308.
    • (1980) New Syntheses with Carbon Monoxide , pp. 242-308
    • Mullen, A.1
  • 4
    • 0035498330 scopus 로고    scopus 로고
    • Kiss, G. Chem. Rev. 2001, 101, 3435-3456.
    • (2001) Chem. Rev , vol.101 , pp. 3435-3456
    • Kiss, G.1
  • 8
    • 33845273790 scopus 로고    scopus 로고
    • For a recent paper on the Pd-catalyzed reaction of alkynes with CO and amines leading to α,β-unsaturated amides, see
    • For a recent paper on the Pd-catalyzed reaction of alkynes with CO and amines leading to α,β-unsaturated amides, see: Li, Y.; Alper, H.; Yu, Z. Org. Lett. 2006, 8, 5199-5201.
    • (2006) Org. Lett , vol.8 , pp. 5199-5201
    • Li, Y.1    Alper, H.2    Yu, Z.3
  • 9
    • 0001357317 scopus 로고    scopus 로고
    • 12-catalyzed reaction of alkynes with CO and amines leading to α,β-unsaturated amides, see: Joh, T.; Doyama, K.; Onitsuka, K.; Shiohara, T.; Takahashi, S. Organometallics 1991, 10, 2493-2498.
    • 12-catalyzed reaction of alkynes with CO and amines leading to α,β-unsaturated amides, see: Joh, T.; Doyama, K.; Onitsuka, K.; Shiohara, T.; Takahashi, S. Organometallics 1991, 10, 2493-2498.
  • 10
    • 0000171099 scopus 로고    scopus 로고
    • For our papers on chelation-assisted carbonylation at C-H bonds, see
    • For our papers on chelation-assisted carbonylation at C-H bonds, see: Chatani, N.; Fukuyama, T.; Kakiuchi, F.; Murai, S. J. Am. Chem. Soc. 1996, 118, 493-494.
    • (1996) J. Am. Chem. Soc , vol.118 , pp. 493-494
    • Chatani, N.1    Fukuyama, T.2    Kakiuchi, F.3    Murai, S.4
  • 25
    • 32344450853 scopus 로고    scopus 로고
    • For recent selected reviews on chelation-assisted transformations, see
    • For recent selected reviews on chelation-assisted transformations, see: Itami, K.; Yoshida, J. Synlett 2006, 157-180.
    • (2006) Synlett , pp. 157-180
    • Itami, K.1    Yoshida, J.2
  • 35
    • 12944303660 scopus 로고    scopus 로고
    • Isocyanates are well-known to participate in cycloaddition reactions as two-atom components. For recent papers, see
    • Isocyanates are well-known to participate in cycloaddition reactions as two-atom components. For recent papers, see: Yamamoto, Y.; Kinpara, K.; Saigoku, T.; Takagishi, H.; Okuda, S.; Nishiyama, H.; Itoh, K. J. Am. Chem. Soc. 2005, 127, 605-613;
    • (2005) J. Am. Chem. Soc , vol.127 , pp. 605-613
    • Yamamoto, Y.1    Kinpara, K.2    Saigoku, T.3    Takagishi, H.4    Okuda, S.5    Nishiyama, H.6    Itoh, K.7


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.