By Alan R. Katritzky, Richard J. K. Taylor and Janine Cossy
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Extra resources for Comprehensive Organic Functional Group Transformations II: v. 1(Carbon with No Attached Heteroatoms)
Among other ethers the recent report that prenyl ethers are reductively cleaved by zirconium chloride/sodium borohydride in the presence of a range of other similar systems (including benzyl ethers and prenyl esters) merits further study <2003TL2525>, while examples of the reduction of -alkoxyketones by samarium iodide continue to be reported <1995JOC1110, 2000T351>. OH O BnO BnO Pd/C, H2, EtOH O BnO 89% O BnO OMe ð42Þ OMe OBn OBn Boc N Boc Pd/C or Pd(OH)2, H2 N ð43Þ 90–100% Ph OBn Ph The use of triethylsilane in the presence of catalytic amounts of tri(pentafluorophenyl)borane shows promise in the reduction of alkyl ethers <2000JOC6179>.
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Comprehensive Organic Functional Group Transformations II: v. 1(Carbon with No Attached Heteroatoms) by Alan R. Katritzky, Richard J. K. Taylor and Janine Cossy