메뉴 건너뛰기




Volumn 130, Issue 22, 2008, Pages 6944-6945

Au(I)-catalyzed efficient synthesis of functionalized bicyclo[3.2.0] heptanes

Author keywords

[No Author keywords available]

Indexed keywords

BICYCLO[3.2.0]HEPTANE DERIVATIVE; GOLD;

EID: 44449159964     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja802294t     Document Type: Article
Times cited : (102)

References (25)
  • 1
    • 34547510627 scopus 로고    scopus 로고
    • For recent reviews on Au/Pt catalysis, see: (a) Hashmi, A. S. K. Chem. Rev. 2007, 107, 3180-3211.
    • For recent reviews on Au/Pt catalysis, see: (a) Hashmi, A. S. K. Chem. Rev. 2007, 107, 3180-3211.
  • 7
    • 33846150040 scopus 로고    scopus 로고
    • For a review, see: a
    • For a review, see: (a) Patil, N. T.; Yamamoto, Y. Arkivoc 2007, v, 6-19.
    • (2007) Arkivoc , vol.5 , pp. 6-19
    • Patil, N.T.1    Yamamoto, Y.2
  • 13
    • 33846088547 scopus 로고    scopus 로고
    • For a review, see: f
    • For a review, see: (f) Kusama, H.; Iwasawa, N. Chem. Lett. 2006, 35, 1082-1087.
    • (2006) Chem. Lett , vol.35 , pp. 1082-1087
    • Kusama, H.1    Iwasawa, N.2
  • 15
    • 0001195079 scopus 로고    scopus 로고
    • The strain energy of parent bicycle[3.2.0]heptane was estimated as 30.48 kcal/mol; for reference, see: Engler, E. M.; Andose, J. D.; Schlever, P. V. J. Am. Chem. Soc. 1973, 95, 8005-8025.
    • The strain energy of parent bicycle[3.2.0]heptane was estimated as 30.48 kcal/mol; for reference, see: Engler, E. M.; Andose, J. D.; Schlever, P. V. J. Am. Chem. Soc. 1973, 95, 8005-8025.
  • 19
    • 34748850041 scopus 로고    scopus 로고
    • 1,3-Bis(2,6-diisopropylphenyl)imidazol-2-ylidenegold(I) bis(trifluoromethanesulfonyl)imide. For its synthesis, see: (a) Ricard, L.; Gagosz, F. Organometallics 2007, 26, 4704-4707
    • 1,3-Bis(2,6-diisopropylphenyl)imidazol-2-ylidenegold(I) bis(trifluoromethanesulfonyl)imide. For its synthesis, see: (a) Ricard, L.; Gagosz, F. Organometallics 2007, 26, 4704-4707
  • 20
    • 34447320531 scopus 로고    scopus 로고
    • For its catalysis, see: b
    • For its catalysis, see: (b) Li, G.; Zhang, L. Angew. Chem., Int. Ed. 2007, 46, 5156-5159.
    • (2007) Angew. Chem., Int. Ed , vol.46 , pp. 5156-5159
    • Li, G.1    Zhang, L.2
  • 23
    • 44449096101 scopus 로고    scopus 로고
    • 2 at room temperature. However, slow decomposition was observed at 80°C.
    • 2 at room temperature. However, slow decomposition was observed at 80°C.
  • 24
    • 44449119930 scopus 로고    scopus 로고
    • 1H NMR gave a ratio of 5/1 for the two compounds and a combined yield of more than 90%.
    • 1H NMR gave a ratio of 5/1 for the two compounds and a combined yield of more than 90%.
  • 25
    • 44449120817 scopus 로고    scopus 로고
    • In our later scope studies, it became apparent that AuCl3 and PtCl2 did not stay catalytically active in the reaction after 15 to 30 min
    • 2 did not stay catalytically active in the reaction after 15 to 30 min.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.