Generation of an N-Isocyanatoimime and its Cycloadditions leading to Sterically Stabilised Zwitterions

DOI: 10.1039/c39820000766

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Journal of the Chemical Society. Chemical communications p. 766 - 768 (1982)

Update date:2022-08-03

Topics:: Authors:

Jones, David W.

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Article abstract of DOI:10.1039/c39820000766

The reaction between 1,3-dimesitylbenzofuran and 4-phenyltriazoline-3,5-dione affords a sterically stabilised zwitterion that at 110 deg C decomposes to the N-isocyanatoimine (13) which adds to olefinic and acetylenic traps to form stable zwitterions of the type (6) and (9), respectively; (9) isomerises to (10) at 110 deg C.

Full text of DOI:10.1039/c39820000766

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Generation of an N-Isocyanatoimime and its Cycloadditions leading to Sterically Stabilised Zwitterions

DOI: 10.1039/c39820000766

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Article abstract of DOI:10.1039/c39820000766

Full text of DOI:10.1039/c39820000766

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