MARC record from Internet Archive

LEADER: 04903cam 2200769Ia 4500
001 ocn162565599
003 OCoLC
005 20200508034543.0
008 070806s1995 enka ob 001 0 eng d
006 m o d
007 cr cn|||||||||
040 $aOPELS$beng$epn$cOPELS$dOCLCG$dOPELS$dOCLCQ$dOCLCF$dOCLCO$dN$T$dYDXCP$dIDEBK$dMERUC$dOCLCQ$dDEBSZ$dD6H$dLEAUB$dOL$
019 $a212162779
020 $a9780080420806
020 $a008042080X
020 $a9780080529011
020 $a0080529011
035 $a(OCoLC)162565599$z(OCoLC)212162779
037 $a123809:119442$bElsevier Science & Technology$nhttp://www.sciencedirect.com
050 4 $aQD325$b.L39 1995eb
070 $aQD325.L39$b1995
072 0 $aX500
072 7 $aSCI$x013040$2bisacsh
082 04 $a547.7/83$222
100 1 $aLevy, D. E.$q(Daniel E.)
245 14 $aThe chemistry of C-glycosides /$cDaniel E. Levy and Cho Tang.
250 $a1st ed.
260 $aOxford, OX, U.K. ;$aTarrytown, N.Y., U.S.A. :$bPergamon,$c1995.
300 $a1 online resource (xiv, 291 pages) :$billustrations.
336 $atext$btxt$2rdacontent
337 $acomputer$bc$2rdamedia
338 $aonline resource$bcr$2rdacarrier
490 1 $aTetrahedron organic chemistry series ;$vv. 13
520 $aIn recent years <IT>C</IT>-glycoside chemistry has been one of the main topics in carbohydrate chemistry, not only because of the synthetic challenges posed, but also because <IT>C</IT>-glycosides have the potential to serve as carbohydrate analogues resistant to metabolic processes. Consequently, this class of compounds is currently receiving much interest as a potential source of therapeutic agents for clinical use. This book provides a broad coverage of the various synthetic methods available for the preparation of <IT>C</IT>-glycosides, and illustrates the interesting breadth of connections between carbohydrate chemistry and modern general synthetic organic chemistry by including topics such as transition-metal catalysis, radical chemistry, cycloaddition and rearrangement processes. In addition, in the final chapter of the book, the syntheses of C-di and trisaccharides reported through 1994 are reviewed. This well organised account of the synthetic chemistry in this field will prove to be very valuable to a wide range of researchers and advanced students, both as an introduction to the topic and for reference.
505 0 $aIntroduction. Electrophilic Substitutions. Nucleophilic Sugar Substitutions. Transition Metal Mediated <IT>C</IT>-Glycosidations. Anomeric Radicals. Rearrangements and Cycloadditions. Sugar Ring Formations. Syntheses of <IT>C</IT>-Di and Trisaccharides. Index.
504 $aIncludes bibliographical references and index.
588 0 $aPrint version record.
650 0 $aGlycosides.
650 7 $aSCIENCE$xChemistry$xOrganic.$2bisacsh
650 7 $aGlycosides.$2fast$0(OCoLC)fst00943801
650 17 $aGlycosiden.$2gtt
650 7 $aCarboidratos.$2larpcal
655 4 $aElectronic books.
655 0 $aElectronic books.
700 1 $aTang, C.$q(Cho)
776 08 $iPrint version:$aLevy, D.E. (Daniel E.).$tChemistry of C-glycosides.$b1st ed.$dOxford, OX, U.K. ; Tarrytown, N.Y., U.S.A. : Pergamon, 1995$z008042080X$z9780080420806$w(DLC) 95038444$w(OCoLC)33047059
830 0 $aTetrahedron organic chemistry series ;$vv. 13.
856 40 $3EBSCOhost$uhttp://search.ebscohost.com/login.aspx?direct=true&scope=site&db=nlebk&db=nlabk&AN=219904
856 40 $3MyiLibrary$uhttp://www.myilibrary.com?id=118638
856 40 $3ScienceDirect$uhttp://www.sciencedirect.com/science/book/9780080420806
856 41 $3Table of contents$uhttp://catdir.loc.gov/catdir/enhancements/fy0602/95038444-t.html
856 42 $3Publisher description$uhttp://catdir.loc.gov/catdir/enhancements/fy0602/95038444-d.html
856 4 $uhttp://www.sciencedirect.com/science/bookseries/14601567/13$xVerlag
856 40 $3ScienceDirect$uhttp://dproxy.library.dc-uoit.ca/login?url=https://www.sciencedirect.com/science/book/9780080420806$zeBook available for Durham College via Elsevier. Click link to access
856 40 $3ScienceDirect$uhttp://dproxy.library.dc-uoit.ca/login?url=https://www.sciencedirect.com/science/bookseries/14601567/13$zeSeries Volume available for Durham College via Elsevier. Click link to access
856 40 $3ScienceDirect$uhttps://ezproxy.aub.edu.lb/login?url=http://www.sciencedirect.com/science/book/9780080420806$zClick for electronic access to e-book.
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