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I'm running a phosphorylation reaction to produce an organic phosphate salt as my product. Structure RPO(OH)(ONBu4). After isolating the pure product, I want to fully deprotonate the phosphate and...
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One of the molecules I designed to synthesized is a alpha, beta unsaturated lactone with a halogen alpha to the carbonyl. To construct the lactone I'm planning to perform a RCM reaction; however,...
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Well, I already know that this reagent is a little bit tricky because of the quench part but my problem is that in a chlorination of alcohol using POCl3 I do TLC and it looks like all the start...
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