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4OMe-p], the precursor intermediate compound of product 3aa, was isolated with 65% yield by the reaction between azido-alkyne 4a and iodide 5a under the optimised reaction conditions except that no heating was performed and stirring was done at rt for 1.0 h. Interestingly, the elimination of CuI from this reaction afforded the intermediate D, albeit only with 16% yield even after stirring at rt for 14 h.
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The crystal data has been deposited at Cambridge Crystallographic Data Centre. The copies of the data can be obtained free of charge via or CCDC, 12 Union Road, Cambridge CB2 1EZ, UK.CCDC no for product 3cj, 804536 CCDC no for product 2 ′′ i, 804692
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66
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34250856292
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2 in presence of trace amount of dimethylamine (see: I. Beletskaya, and A. V. Cheprakov, Chem. Rev., 2000, 100, 3009) which is being produced from the decomposition of DMF at elevated temperature or as contaminant in the DMF (see
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