LEADER 03152nam 2200697 450 001 9910452501703321 005 20200520144314.0 010 $a0-19-935286-0 010 $a0-19-998799-8 035 $a(CKB)2550000001123573 035 $a(EBL)1480994 035 $a(OCoLC)861559203 035 $a(SSID)ssj0001001098 035 $a(PQKBManifestationID)12394591 035 $a(PQKBTitleCode)TC0001001098 035 $a(PQKBWorkID)10966332 035 $a(PQKB)11314118 035 $a(StDuBDS)EDZ0000141818 035 $a(MiAaPQ)EBC1480994 035 $a(Au-PeEL)EBL1480994 035 $a(CaPaEBR)ebr10775446 035 $a(CaONFJC)MIL525290 035 $a(EXLCZ)992550000001123573 100 $a20120918d2013 uy| 0 101 0 $aeng 135 $aur|n|---||||| 181 $ctxt 182 $cc 183 $acr 200 00$aCT imaging $epractical physics, artifacts, and pitfalls /$feditor, Alexander C. Mamourian ; contributors, Harold Litt [and three others] 210 1$aNew York :$cOxford University Press,$d2013. 215 $a1 online resource (253 p.) 300 $aDescription based upon print version of record. 311 $a0-19-978260-1 311 $a1-299-94039-0 320 $aIncludes bibliographical references and index. 327 $aHistory and physics of CT imaging / Alexander C. Mamourian -- Radiation safety and risks / Alexander C. Mamourian and Josef P. Debbins -- CT cardiac imaging / Supratik Moulik and Harold Litt -- Cardiac CT artifacts and pitfalls / Supratik Moulik and Harold Litt -- Neuro CT artifacts / Alex C. Mamourian -- Neuro CT pitfalls / Alex C. Mamourian -- Body CT artifacts / Nicholas Papanicolaou -- Body CT pitfalls / Nicholas Papanicolaou -- Test questions / Alexander C. Mamourian. 330 $aCT imaging has become a mainstay of medical imaging. After 30 years this is a mature technology but the accumulation of innovations over the past decades have given it extraordinary capabilities and new applications continue to emerge. In this book Alex Mamourian uses early CT technology to explain the fundamentals of CT imaging and then builds on that base to explain how innovations such as slip-ring and multidetector arrays allow for rapid, high resolution imaging. This book covers complex applications such as CT cardiac imaging and dual-source dual-energy CT scanning as well as the pitfalls 606 $aTomography 606 $aNervous system$xRadiography 606 $aRadiation dosimetry 606 $aRadiation$xSafety measures 606 $aWhole body imaging 606 $aHeart$xTomography 608 $aElectronic books. 615 0$aTomography. 615 0$aNervous system$xRadiography. 615 0$aRadiation dosimetry. 615 0$aRadiation$xSafety measures. 615 0$aWhole body imaging. 615 0$aHeart$xTomography. 676 $a616.07/5722 701 $aMamourian$b Alexander C$0905340 701 $aLitt$b Harold I$0905341 801 0$bMiAaPQ 801 1$bMiAaPQ 801 2$bMiAaPQ 906 $aBOOK 912 $a9910452501703321 996 $aCT imaging$92024966 997 $aUNINA LEADER 06111nam 22020053a 450 001 9910346843703321 005 20250203235429.0 010 $a9783039212040 010 $a3039212044 024 8 $a10.3390/books978-3-03921-204-0 035 $a(CKB)4920000000095203 035 $a(oapen)https://directory.doabooks.org/handle/20.500.12854/40763 035 $a(ScCtBLL)ad6a08ac-67ad-4469-b311-ec8e9468e349 035 $a(OCoLC)1126116469 035 $a(oapen)doab40763 035 $a(EXLCZ)994920000000095203 100 $a20250203i20192019 uu 101 0 $aeng 135 $aurmn|---annan 181 $ctxt$2rdacontent 182 $cc$2rdamedia 183 $acr$2rdacarrier 200 00$aAmide Bond Activation$fMichal Szostak 210 $cMDPI - Multidisciplinary Digital Publishing Institute$d2019 210 1$aBasel, Switzerland :$cMDPI,$d2019. 215 $a1 electronic resource (466 p.) 311 08$a9783039212033 311 08$a3039212036 330 $aThe amide bond represents a privileged motif in chemistry. The recent years have witnessed an explosion of interest in the development of new chemical transformations of amides. These developments cover an impressive range of catalytic N-C bond activation in electrophilic, Lewis acid, radical, and nucleophilic reaction pathways, among other transformations. Equally relevant are structural and theoretical studies that provide the basis for chemoselective manipulation of amidic resonance. This monograph on amide bonds offers a broad survey of recent advances in activation of amides and addresses various approaches in the field. 606 $aChemistry$2bicssc 610 $aN-heterocyclic carbene 610 $anon planar amide 610 $aruthenium (Ru) 610 $aphysical organic chemistry 610 $agemcitabine prodrug 610 $apyramidal amides 610 $abridged sultams 610 $acatalysis 610 $adipeptides 610 $aN-(1-naphthyl)acetamide 610 $aC-N ? bond cleavage 610 $asteric effects 610 $apeptide bond cleavage 610 $atransition-metal-free 610 $apalladium 610 $aN-heterocyclic carbenes (NHCs) 610 $aaddition reaction 610 $aC?O activation 610 $arhodium 610 $ametal complexes 610 $acarbanions 610 $athioamidation 610 $aamide bond 610 $aintramolecular catalysis 610 $aantiviral activity 610 $aadditivity principle 610 $apre-catalysts 610 $aC?N bond cleavage 610 $abridged lactams 610 $aC?H acidity 610 $aarynes 610 $atwisted amides 610 $aorganic synthesis 610 $aamination 610 $aSuzuki-Miyaura 610 $atert-butyl 610 $acyclopentadienyl complexes 610 $aC-S formation 610 $aenzymes 610 $aDFT study 610 $asulfonamide bond 610 $aN 610 $aHERON reaction 610 $aprimaquine 610 $aentropy 610 $aamide activation 610 $aamidation 610 $asynthesis 610 $aamide hydrolysis 610 $acarbonylicity 610 $aamide bond activation 610 $aamide bond resonance 610 $aaminosulfonylation 610 $amolecular dynamics 610 $amodel compound 610 $ain situ 610 $aamide 610 $ahomogeneous catalysis 610 $aheterocycles 610 $aanomeric effect 610 $amulti-component coupling reaction 610 $akinetic 610 $aexcited state 610 $aC?H bond cleavage 610 $apalladium catalysis 610 $aamides 610 $athiourea 610 $aformylation 610 $aalkynes 610 $acis/trans isomerization 610 $aamide C?N bond activation 610 $aintein 610 $aC-H functionalization 610 $asuccindiamide 610 $aamide bonds 610 $acrown ether 610 $aaminoacylation 610 $adirecting groups 610 $acytostatic activity 610 $areaction thermodynamics 610 $aacyl transfer 610 $atransition metals 610 $aN-dimethylformamide 610 $aDMAc 610 $aacylative cross-coupling 610 $aC-H/C-N activation 610 $anickel catalysis 610 $aantibacterial screening 610 $asodium 610 $aaryl thioamides 610 $aWinkler-Dunitz parameters 610 $acatalyst 610 $aN-dimethylacetamide 610 $abase-catalyed hydrolysis 610 $anitrogen heterocycles 610 $across-coupling 610 $ainsertion 610 $aamidicity 610 $anitro-aci tautomerism 610 $aactivation 610 $acarbonylation 610 $atransamidation 610 $aamine 610 $adistortion 610 $aPd-catalysis 610 $arotational barrier energy 610 $ahypersensitivity 610 $aN?C activation 610 $ametabolic stability 610 $a[2+2+2] annulation 610 $atwisted amide 610 $aprotease 610 $acyanation 610 $aamide resonance 610 $atrialkylborane 610 $acatalysts 610 $abiofilm eradication 610 $apharmacokinetics 610 $apancreatic cancer cells 610 $aDMF 610 $aaryl esters 610 $aMichael acceptor 610 $afumardiamide 610 $awater solvation 610 $aester bond activation 610 $acyclization 610 $anuclear magnetic resonance 610 $asecondary amides 610 $areaction mechanism 610 $adensity functional theory 610 $adensity-functional theory 610 $aamino acid transporters 615 7$aChemistry 700 $aSzostak$b Micha?$01781579 801 0$bScCtBLL 801 1$bScCtBLL 906 $aBOOK 912 $a9910346843703321 996 $aAmide Bond Activation$94487035 997 $aUNINA