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- W2072034218 abstract "Abstract Continuing our studies on the specific ortho substitution reaction of anilines,2 we tried to extend this methodology to directed aldol condensation3. Namely, N-cyclohexylidencyclohexylamine 1 was treated with boron trichloride and triethylamine in dichloromethane giving N-cyclohexyl-N-1-cyclohexenylaminodi-chloroborane 2, to our knowledge, a new type of aminohaloborane. Similar treatment of N-2-butyliden-cyclohexylamine 3 gave N-cyclohexyl-N-2-butenylamino-dichloroborane (a mixture of E and Z isomers) 4. The physical data satisfied the assigned structures." @default.
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- W2072034218 date "1979-01-01" @default.
- W2072034218 modified "2023-09-26" @default.
- W2072034218 title "Aminohaloborane in Organic Synthesis. IV.<sup>1</sup>A Directed Aldol Condensation Using Vinylaminodichloroborane" @default.
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- W2072034218 doi "https://doi.org/10.1080/00397917908060955" @default.
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