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- 674. The mechanism and scope of an N-oxide rearrangement. M. S. Habib, C. W. Rees
, J. Chem. Soc.
, 1960
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- To each his own: isonitriles for all flavors. Functionalized isocyanides as valuable tools in organic synthesis. Mariateresa Giustiniano, Andrea Basso, Valentina Mercalli, Alberto Massarotti, Ettore Novellino, Gian Cesare Tron, Jieping Zhu
, Chem. Soc. Rev.
, 2017
, 46
, 1295
- Visible-light-mediated three-component Minisci reaction for heteroarylethyl alcohols synthesis. Jianyang Dong, Fuyang Yue, Jianhua Liu, Hongjian Song, Yuxiu Liu, Qingmin Wang
, Green Chem.
, 2021
, 23
, 7963
- Photochemistry of methoxy-substituted quinoline and isoquinoline N-oxides. Angelo Albini, Elisa Fasani, Lucia Maggi Dacrema
, J. Chem. Soc., Perkin Trans. 1
, 1980
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- 14N chemical shifts in some hydroxyquinolines. P. Hampson, A. Mathias
, Chem. Commun. (London)
, 1967
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- Organic chemistry
, J. Chem. Soc., Abstr.
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- Index of subjects
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- Index of subjects
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- 373. Cinnolines. Part XXXI. The nature of the C(3)-position. Some experiments with 3-substituted cinnolines. E. J. Alford, K. Schofield
, J. Chem. Soc.
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