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- W2912486216 abstract "This paper reports the tandem reaction strategy of the Passerini/Staudinger/aza-Wittig reaction based on the in situ capture of isocyanides. According to this strategy, isocyanides are synthesized in situ and immediately work as the substrate for the Passerini reaction and postmodification tandem reaction in one pot. In addition, two types of new compounds, 5-oxo-3,5-dihydrobenzo[ e][1,4]oxazepines and 6-oxo-5,6-dihydro-2 H-1,4-oxazines, were synthesized using the tandem reaction strategy that includes five-step transformations in one pot." @default.
- W2912486216 created "2019-02-21" @default.
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- W2912486216 date "2019-01-24" @default.
- W2912486216 modified "2023-10-03" @default.
- W2912486216 title "Odorless Isocyanide Chemistry: One-Pot Synthesis of Heterocycles via the Passerini and Postmodification Tandem Reaction Based on the in Situ Capture of Isocyanides" @default.
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- W2912486216 doi "https://doi.org/10.1021/acs.joc.8b03242" @default.
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