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Lewis Acid-Mediated Formation of 1,3-Disubstituted Spiro[cyclopropane-1,2′-indanes]: The Activating Effect of the Cyclopropane Walsh Orbital

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NIAID Data Ecosystem2026-03-11 收录
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https://figshare.com/articles/dataset/Lewis_Acid-Mediated_Formation_of_1_3-Disubstituted_Spiro_cyclopropane-1_2_-indanes_The_Activating_Effect_of_the_Cyclopropane_Walsh_Orbital/11905251
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资源简介:
By virtue of its alkylidenecyclopropane moiety, 2-(cyclopropylidenemethyl)­benzaldehyde reacts with a range of amines and thiols under Lewis acid catalysis. These reactions yield 1,3-bis­(arylamino) and 1,3-bis­(arylthio and alkylthio)­indanes, respectively, which are spirolinked to the cyclopropane ring at carbon 2. The reaction mechanism, and the peculiar contribution of the cyclopropane ring, have been scrutinized via DFT calculations.
创建时间:
2020-02-20
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