LEADER 02938nam 2200661Ia 450 001 9910437798103321 005 20200520144314.0 010 $a1-283-63167-9 010 $a9786613944122 010 $a3-642-32051-1 024 7 $a10.1007/978-3-642-32051-4 035 $a(CKB)2670000000250604 035 $a(EBL)1030350 035 $a(OCoLC)809794112 035 $a(SSID)ssj0000738579 035 $a(PQKBManifestationID)11378515 035 $a(PQKBTitleCode)TC0000738579 035 $a(PQKBWorkID)10792158 035 $a(PQKB)11132897 035 $a(DE-He213)978-3-642-32051-4 035 $a(MiAaPQ)EBC1030350 035 $a(PPN)168320908 035 $a(EXLCZ)992670000000250604 100 $a20120922h20122013 uy 0 101 0 $aeng 135 $aur|n|---||||| 181 $ctxt 182 $cc 183 $acr 200 10$aNovel synthetic chemistry of ureas and amides $edoctoral thesis accepted by the University of Bristol, UK /$fMarc Hutchby 205 $a1st ed. 2013. 210 $aHeidelberg $cSpringer$d2012, c2013 215 $a1 online resource (178 p.) 225 1 $aSpringer theses : recognizing outstanding Ph.D. research,$x2190-5053 300 $aDescription based upon print version of record. 311 $a3-642-44890-9 311 $a3-642-32050-3 320 $aIncludes bibliographical references. 327 $aTransition metal catalysis -- Palladium catalysis -- Pd(II) catalysed aminocarbonylation of alkenes -- Carbonylation of aryl ureas -- Urea Hydrolysis -- Amide hydrolysis. 330 $aIn this thesis, the author investigates the chemistry and application of molecules containing urea and amide bonds. These bonds are some of the strongest known and are fundamental to biological processes. The author describes his discovery that sterically hindered ureas undergo solvolysis at room temperature under neutral conditions. This is a remarkable finding, since ureas are inert under these conditions and a general rule of chemistry is that hindered substrates are less reactive. Remarkably, the author translates these results to the correspondingly sterically hindered amides. This thesis has resulted in a number of outstanding publications in high profile journals. The unique method for breaking urea and amide bonds developed in this study is likely to have far reaching consequences for biological protein manipulation. 410 0$aSpringer theses. 606 $aOrganic compounds$xSynthesis 606 $aChemical bonds 606 $aUrea 606 $aAmides 615 0$aOrganic compounds$xSynthesis. 615 0$aChemical bonds. 615 0$aUrea. 615 0$aAmides. 676 $a660.6 700 $aHutchby$b Marc$01059105 801 0$bMiAaPQ 801 1$bMiAaPQ 801 2$bMiAaPQ 906 $aBOOK 912 $a9910437798103321 996 $aNovel Synthetic Chemistry of Ureas and Amides$92504168 997 $aUNINA