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MARC Record from marc_columbia

Record ID marc_columbia/Columbia-extract-20221130-031.mrc:259493168:3419
Source marc_columbia
Download Link /show-records/marc_columbia/Columbia-extract-20221130-031.mrc:259493168:3419?format=raw

LEADER: 03419cam a2200541Ma 4500
001 15133302
005 20220703234050.0
006 m o d
007 cr |n|||||||||
008 180628s2001 ne a ob 001 0 eng d
035 $a(OCoLC)on1041882947
035 $a(NNC)15133302
040 $aYDX$beng$cYDX$dOCLCQ$dYDX$dK6U$dOCLCO$dSFB$dOCLCO$dOCLCF$dOCLCO
019 $a1260361657
020 $a9781482283143$q(electronic bk.)
020 $a148228314X$q(electronic bk.)
020 $z9789056993245
020 $z9056993240
020 $a9780429153327$q(electronic bk.)
020 $a0429153325$q(electronic bk.)
035 $a(OCoLC)1041882947$z(OCoLC)1260361657
050 4 $aQP625.N88$bS55 2001
060 4 $a2003 F-925
060 4 $aQV 185$bS611n 2001
082 04 $a540
049 $aZCUA
100 1 $aSimons, Claire.
245 10 $aNucleoside mimetics :$btheir chemistry and biological properties /$cClaire Simons.
260 $aAmsterdam :$bGordon and Breach Science Publishers,$c©2001.
300 $a1 online resource.
336 $atext$btxt$2rdacontent
337 $acomputer$bc$2rdamedia
338 $aonline resource$bcr$2rdacarrier
490 1 $aAdvanced chemistry texts ;$vv. 3
504 $aIncludes bibliographical references and index.
505 00 $tStructure of Nucleosides --$tStructure of the Sugar Moiety --$tStructure of the Heterocyclic Base Moiety --$tNucleoside Conformation --$tGlycosyl Link Geometry --$tC4'-C5' Bond Geometry --$tRing Puckering --$tNomenclature --$tSpectroscopy --$tMass Spectroscopy --$tNMR Spectroscopy --$tBiological Properties --$tRNA and DNA --$tPurine and Pyrimidine Nucleotide Biosynthesis --$tMechanisms of Action of Nucleoside Mimetics --$tInhibitors Targeted at Reverse Transcriptase --$tInhibitors Targeted at DNA Viruses --$tInhibitors Targeted at Nucleotide Metabolising Enzymes --$tSynthesis of Conventional D-Nucleosides --$tFirst Syntheses of the Natural Ribonucleosides --$tStereospecificity in Nucleoside Synthesis --$tCoupling Methods --$tCoupling of Heterocyclic Salts with Halo-Sugars --$tVorbruggen Procedure --$tNucleoside Synthesis from Glycals --$tGlycosylamine Procedure --$tEnzymatic Synthesis --$tSugar Modifications --$tSugar Modifications via Anhydronucleosides --$tSugar Modifications via Epoxides --$tDeoxygenation --$tAzido and Amino Sugars --$tHalogenation --$t2'- and 3'-C-Nucleosides --$tHeterocyclic Base Modifications --$tPyrimidine Modifications --$tPurine Modifications --$tSugar Modified Nucleosides --$tIsonucleosides --$t2'-Isonucleosides --$t3'-Isonucleosides --$t4'-Substituted Nucleosides --$t4'-Thinoucleosides --$t4'-Aza-nucleosides --$tDioxo-, Oxathio- and Dithio-Nucleosides --$tOxaza-, Isoxa- and Thiaza-Nucleosides --$tRing Size --$tOxetanocin-A and Derivatives --$tPyranose Nucleosides --$tSpiro-Nucleosides --$tHeterocyclic Base Modified Nucleosides.
650 0 $aNucleosides.
650 12 $aNucleosides$xchemistry
650 22 $aNucleosides$xclassification
650 22 $aNucleosides$xpharmacology
650 2 $aNucleosides
650 6 $aNucléosides.
650 7 $aNucleosides.$2fast$0(OCoLC)fst01041098
655 0 $aElectronic books.
776 08 $cOriginal$z9789056993245$z9056993240$w(OCoLC)46831031
830 0 $aAdvanced chemistry texts ;$vv. 3.
856 40 $uhttp://www.columbia.edu/cgi-bin/cul/resolve?clio15133302$zTaylor & Francis eBooks
852 8 $blweb$hEBOOKS