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Synlett 2012(4): 642-643
DOI: 10.1055/s-0031-1290334
DOI: 10.1055/s-0031-1290334
SPOTLIGHT
© Georg Thieme Verlag
Stuttgart ˙ New York
Zinc Borohydride
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Publikationsverlauf
Publikationsdatum:
13. Februar 2012 (online)
Introduction
Zinc borohydride is a neutral reagent employed for the reduction of several types of carbonyl compounds. It is commercially available, but it is also easily prepared by reacting ZnCl2 with NaBH4. [¹] Kotsuki et al. described the selective reduction of thioesters in the presence of other functional groups using Zn(BH4)2 [¹] and Oishi and Nakata described the reduction of chiral β-keto esters with Zn(BH4)2 leading to the corresponding alcohols with high stereoselectivity. [²] This Spotlight summarizes further reactions of zinc borohydride.
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