메뉴 건너뛰기




Volumn 5, Issue 1, 2014, Pages 163-168

Benz[c]indeno[2,1-a]fluorene: A 2,3-naphthoquinodimethane incorporated into an indenofluorene frame

Author keywords

[No Author keywords available]

Indexed keywords

CYCLOADDITIONS; CYCLODIMERIZATION; INDENOFLUORENE; MESITYL GROUPS; NAPHTHALENE RING; QUANTUM CHEMICAL STUDIES; STERIC PROTECTION; X-RAY CRYSTALLOGRAPHIC STRUCTURES;

EID: 84888613670     PISSN: 20416520     EISSN: 20416539     Source Type: Journal    
DOI: 10.1039/c3sc52622d     Document Type: Article
Times cited : (74)

References (57)
  • 4
    • 67650059255 scopus 로고    scopus 로고
    • ed. J. Siegel and Y. Tobe, Thieme, Stuttgart, 483-506
    • H. Sano and J. Nishimura, Science of Synthesis, ed., J. Siegel, and, Y. Tobe, Thieme, Stuttgart, 2009, vol. 45a, pp. 483-506
    • (2009) Science of Synthesis , vol.45
    • Sano, H.1    Nishimura, J.2
  • 23
  • 37
    • 84934908949 scopus 로고    scopus 로고
    • 10.1007/128-2012-376. Recently, Haley and co-workers added a new member of p-QDM, indeno[2,1-c]fluorene, to the indenofluorene family
    • A. G. Fix D. T. Chase M. M. Haley Top. Curr. Chem. 10.1007/128-2012-376
    • Top. Curr. Chem.
    • Fix, A.G.1    Chase, D.T.2    Haley, M.M.3
  • 40
    • 33947435033 scopus 로고
    • Though diol 11 was obtained as a single isomer, its stereochemistry was not determined It should be pointed out that for 11,12-diphenylindeno[2,1-a] fluorene (8c), Le Berre reported that oxygen added to the exo-methylene carbons yielding the corresponding cyclic peroxide which further degradated to give bond cleaved products. 12a Similarly, attempts to prepare NQD derivative 9c resulted in the formation of decomposition products derived from oxygenation at the exo-methylene carbons 12a
    • C. F. Koelsch H. J. Richter J. Org. Chem. 1938 3 465 472
    • (1938) J. Org. Chem. , vol.3 , pp. 465-472
    • Koelsch, C.F.1    Richter, H.J.2
  • 57
    • 0001033243 scopus 로고
    • Le Berre reported that maleic anhydride added to the exo-methylene carbons of 11,12-diphenylindeno[2,1-a]fluorene (8c), though the structure was not concretely established. 12a Similarly, an attempt to prepare NQD derivative 9c in the presence of maleic anhydride gave an adduct at the exo-methylene carbons. 12a On the other hand, we reported that dimesityl derivative 8b did not react with maleic anhydride when a toluene solution of them was heated at 100 °C, 12b showing the efficient protecting effect of the mesityl groups
    • K. K. Baldridge J. S. Siegel J. Am. Chem. Soc. 1992 114 9583 9587
    • (1992) J. Am. Chem. Soc. , vol.114 , pp. 9583-9587
    • Baldridge, K.K.1    Siegel, J.S.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.