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While the intermolecular C-H bond insertion to hydrocarbons as solvent has been reported (reference [4a]), to the best of our knowledge, an intramolecular insertion in a stereoselective manner as shown herein had not been reported before portions of this work were preliminary and orally presented at the 95th Annual Meeting of the Chemical Society of Japan held in Chiba, Japan, March 26-29, 2015; Abstr. 3E5-18 and 3E5-29. However, after almost completion of this study, the following report has appeared
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While the intermolecular C-H bond insertion to hydrocarbons as solvent has been reported (reference [4a]), to the best of our knowledge, an intramolecular insertion in a stereoselective manner as shown herein had not been reported before portions of this work were preliminary and orally presented at the 95th Annual Meeting of the Chemical Society of Japan held in Chiba, Japan, March 26-29, 2015; Abstr. 3E5-18 and 3E5-29. However, after almost completion of this study, the following report has appeared:
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See the Supporting Information.
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As sulfonylimines produced from triazoles have been routinely converted into sulfonylamines for isolation and characterization (see references [3]-[5] and [8a]), the isolation of the former as pure samples is not trivial.
-
As sulfonylimines produced from triazoles have been routinely converted into sulfonylamines for isolation and characterization (see references [3]-[5] and [8a]), the isolation of the former as pure samples is not trivial.
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-
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