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Volumn 12, Issue 18, 2010, Pages 4062-4065

Lewis acid catalyzed inverse electron-demand diels-alder reaction of 1,2-diazines

Author keywords

[No Author keywords available]

Indexed keywords

LEWIS ACID; SINGLE HETEROCYCLIC RINGS;

EID: 77956590825     PISSN: 15237060     EISSN: 15237052     Source Type: Journal    
DOI: 10.1021/ol101701z     Document Type: Article
Times cited : (94)

References (55)
  • 4
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    • For an example for an IEDDA in a total synthesis, see
    • For an example for an IEDDA in a total synthesis, see: Bodwell, G. J.; Li, J. Angew. Chem., Int. Ed. 2002, 41, 3261
    • (2002) Angew. Chem., Int. Ed. , vol.41 , pp. 3261
    • Bodwell, G.J.1    Li, J.2
  • 7
    • 33845376451 scopus 로고
    • For recent examples of IEDDA reactions with triazines, see:
    • Boger, D. L. Chem. Rev. 1986, 86, 781 For recent examples of IEDDA reactions with triazines, see:
    • (1986) Chem. Rev. , vol.86 , pp. 781
    • Boger, D.L.1
  • 32
    • 0038626673 scopus 로고    scopus 로고
    • revision D.02; see Supporting Information
    • Frisch, M. J.; Gaussian 03, revision D.02; see Supporting Information.
    • Gaussian 03
    • Frisch, M.J.1
  • 34
    • 36849021014 scopus 로고    scopus 로고
    • Alternatively, we developed in our laboratory a new Fe-catalyzed method to access 1,2-bis(trimethylsilyl)benzenes:
    • Bettinger, H. F.; Filthaus, M. J. Org. Chem. 2007, 72, 9750 Alternatively, we developed in our laboratory a new Fe-catalyzed method to access 1,2-bis(trimethylsilyl)benzenes:
    • (2007) J. Org. Chem. , vol.72 , pp. 9750
    • Bettinger, H.F.1    Filthaus, M.2
  • 45
    • 77956570345 scopus 로고    scopus 로고
    • 3N) to yield a colorless oil (28.4 mg, 42%)
    • 3N) to yield a colorless oil (28.4 mg, 42%).
  • 46
    • 0000469763 scopus 로고
    • The elimination of the pyrrolidine was completed using m -CPBA
    • The elimination of the pyrrolidine was completed using m -CPBA: Chenard, B. L.; Ronau, R. T.; Schulte, G. K. J. Org. Chem. 1988, 53, 5175
    • (1988) J. Org. Chem. , vol.53 , pp. 5175
    • Chenard, B.L.1    Ronau, R.T.2    Schulte, G.K.3
  • 49
    • 77956583818 scopus 로고    scopus 로고
    • For an example of an IEDDA with 1,2,4-triazenes with enamines, generated in situ, see
    • For an example of an IEDDA with 1,2,4-triazenes with enamines, generated in situ, see
  • 51
    • 77956584855 scopus 로고    scopus 로고
    • The mixture of regioisomers in Table 1, entry 8, is caused by isomerization of the double bond to the exo -position
    • The mixture of regioisomers in Table 1, entry 8, is caused by isomerization of the double bond to the exo -position
  • 53
    • 77956583303 scopus 로고    scopus 로고
    • The elimination to the aromatic product was completed using UV irradiation
    • The elimination to the aromatic product was completed using UV irradiation


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.