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presentation also includes a step-by-step protocol for the lithium acetate method of yeast transformation
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, lithium aluminum hydride, and Grignard reagent can open the epoxide ring. The nucleophilic attack on the
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Alkynes can be reduced to trans-alkenes using sodium or lithium in liquid ammonia. The reaction
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of bromine to 2-butyne in the presence of acetic acid and lithium bromide favors anti addition and
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borohydride (NaBH4) and lithium aluminum hydride (LiAlH4, or LAH), as nucleophilic attack by a free hydride
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