4.5 Article

Palladium/Charcoal-Catalysed Olefin Reduction for the Simple and Efficient Synthesis of Substituted gem -Diborylalkanes

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SYNTHESIS-STUTTGART
卷 55, 期 22, 页码 3799-3808

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GEORG THIEME VERLAG KG
DOI: 10.1055/a-2147-1336

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vinyl geminal B(pin); alkyl geminal B(pin); aryl geminal B(pin); heteroaryl geminal B(pin); reduction; palladium/carbon

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Gem-diborylalkanes, as valuable synthons in diverse C-C bond-forming reactions, have been studied. A Pd-catalysed hydrogenation method for the synthesis of gem-diborylalkanes from gem-diborylalkenes has been reported.
gem-Diborylalkanes have recently emerged as valuable synthons for diverse C-C bond-forming reactions. They represent an im-portant class of bifunctional reagents that can be applied for the syn-thesis of simple to complex skeletons. Herein, we report a Pd-catalysedhydrogenation method for the synthesis of gem-diborylalkanes from the corresponding gem-diborylalkenes, which are themselves prepared from the corresponding aldehydes and ketones using known procedures. In addition, transformations of two representative gem-diboryl-alkane products are discussed leading to a range of functionalised derivatives

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