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0342917770
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note
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The reaction of 2c with 1, followed by in situ treatment with an excess of trimethylamine oxide at 80 °C for 18 h, provided 4-tert-butylcyclohexanone in 457% yield together with 4-tert-butylcyclohex-2-en-1-ol (8%).
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16
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0003624033
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0343788689
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note
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The borylation of (E)-1 -iodo-3,3-dimethylbutene proceeded with retention of starting geometry to provide the corresponding (E)-alkenylboronate in 33% yield. Our synthetic study on the acyclic alkenyl system is as yet incomplete.
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25
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0343352942
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note
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To some extent, a plausible mechanism for the case of aryl halides proposed by us (see Ref. 4b) would refer to the present situation.
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