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Silacyclobutanes trans - 3e and cis - 3e were the only identifiable products of this reaction. Details are provided as Supporting Information
-
Silacyclobutanes trans-3e and cis-3e were the only identifiable products of this reaction. Details are provided as Supporting Information.
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21
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1H NMR spectroscopic analysis of the unpurified reaction mixture.
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The thiophenyl silane analogue of compound 14 was observed as a minor product due to rearrangement of the starting material. Details are provided as Supporting Information
-
The thiophenyl silane analogue of compound 14 was observed as a minor product due to rearrangement of the starting material. Details are provided as Supporting Information.
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77955698910
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The lithiation reaction with silacyclobutane 3a suffered from irreproducibility. Attempts to trap the alkyllithium intermediate with a carbon electrophile were unsuccessful, as were attempts to lithiate the sulfide functionality on oxasilacyclohexane 11a
-
The lithiation reaction with silacyclobutane 3a suffered from irreproducibility. Attempts to trap the alkyllithium intermediate with a carbon electrophile were unsuccessful, as were attempts to lithiate the sulfide functionality on oxasilacyclohexane 11a.
-
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47
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84985631317
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48
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77955703342
-
-
An NOE enhancement was applied to resolve the splitting of this peak
-
An NOE enhancement was applied to resolve the splitting of this peak.
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