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Diels–Alder reactivity of pyrano[3,4-b]indol-3-ones, stable, synthetic equivalents of indole-2,3-quinodimethanes
作者:Christopher J. Moody
DOI:10.1039/c39840000925
日期:——
Pyrano[3,4-b]indol-3-ones (5), synthetic equivalents of indole-2,3-quinodimethanes, undergo Deils–Alder reaction with acetylenes and with benzyne to give carbazoles and benzo[b]carbozoles respectively.
吡喃并[3,4- b ]
吲哚-3-酮(5)是
吲哚-2,3-喹二
甲烷的合成等价物,与
乙炔和苯并炔进行Deils-Alder反应,分别得到
咔唑和苯并[ b ]
咔唑。
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Moody, Christopher J., Journal of the Chemical Society. Perkin transactions I, 1985, p. 2505 - 2508
作者:Moody, Christopher J.
DOI:——
日期:——
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MATLIN, STEPHEN A.;BARRON, KENNEM, J. CHEM. RES. MICROFICHE ,(1990) N8, C. 246-247
作者:MATLIN, STEPHEN A.、BARRON, KENNEM
DOI:——
日期:——
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MOODY, C. J., J. CHEM. SOC. PERKIN TRANS., 1985, N 11, 2505-2508
作者:MOODY, C. J.
DOI:——
日期:——
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MOODY, CH. J., J. CHEM. SOC. CHEM. COMMUN., 1984, N 14, 925-926
作者:MOODY, CH. J.
DOI:——
日期:——