| Record ID | ia:carbonrichcompou0000unse |
| Source | Internet Archive |
| Download MARC XML | https://archive.org/download/carbonrichcompou0000unse/carbonrichcompou0000unse_marc.xml |
| Download MARC binary | https://www.archive.org/download/carbonrichcompou0000unse/carbonrichcompou0000unse_meta.mrc |
LEADER: 03994cam 2200781Ma 4500
001 ocn213934309
003 OCoLC
005 20220809130837.0
008 980922s1998 gw a ob 001 0 eng d
006 m o d
007 cr un|---|||||
040 $aCUT$beng$epn$cCUT$dAZN$dYNG$dOHI$dCSU$dOCLCQ$dOCLCE$dOCLCO$dOCLCQ$dOCLCA$dUV0$dOCLCO$dGW5XE$dOCLCF$dOCLCQ$dGZM$dUAB$dOCLCQ$dAU@$dOCLCQ$dCANPU$dTKN$dLEAUB$dOCLCO
019 $a47994116$a644324369$a809467297$a1058108159$a1078839276$a1125719422
020 $a9783540696919$q(electronic bk.)
020 $a3540696911$q(electronic bk.)
020 $z3540641106
020 $z9783540641100
020 $z3540653015
020 $z9783540653011
020 $z3642083811
020 $z9783642083815
024 7 $a10.1007/3-540-69691-1$2doi
035 $a(OCoLC)213934309$z(OCoLC)47994116$z(OCoLC)644324369$z(OCoLC)809467297$z(OCoLC)1058108159$z(OCoLC)1078839276$z(OCoLC)1125719422
050 4 $aQD1$b.F58 vol. 196eb
072 7 $aQD$2lcco
072 7 $aPNN$2bicssc
072 7 $aSCI013040$2bisacsh
082 04 $a547$223
245 00 $aCarbon Rich compounds /$cvolume editor, A. de Meijere ; with contributions by A. de Meijere [and others].
264 1 $aBerlin ;$aNew York :$bSpringer,$c[1998]
264 4 $c©1998
300 $a1 online resource (231 pages) :$billustrations
336 $atext$btxt$2rdacontent
337 $acomputer$bc$2rdamedia
338 $aonline resource$bcr$2rdacarrier
347 $atext file$bPDF$2rda
490 1 $aTopics in current chemistry,$x0340-1022 ;$v196
504 $aIncludes bibliographical references and index.
505 0 $av. 1. Carbon-rich compounds -- v. 2. Macrocyclic oligoacetylenes and other linearly conjugated systems.
520 $aCarbon Rich Compounds are defined here as carbon skeletons with a carbon to hydrogen ratio of 1:(=<1) which includes all-carbon compounds (i.e. carbon allotropes). The current volume covers modern methods for the preparation and transformation of polycyclic aromatic compounds including substructures of C60-fullerene and novel highly complex cyclophanes. A graph theoretical treatment presents a substitution rule, allowing the description of already existing structures and also the definition of new challenging synthetic targets. In the second part of this volume, the synthesis and unique chemistry of oligocyclic compounds consisting of five- and six-membered rings, so-called centro-polyhydrindanes as well as oligoquinanes, in particular highly unsaturated ones, are discussed.
588 0 $aPrint version record.
546 $aEnglish.
650 0 $aCarbon compounds.
650 0 $aAromatic compounds.
650 6 $aCarbone$xComposés.
650 6 $aComposés aromatiques.
650 7 $aAromatic compounds.$2fast$0(OCoLC)fst00815019
650 7 $aCarbon compounds.$2fast$0(OCoLC)fst00846803
650 7 $aCarbone$xComposés organiques.$2ram
650 7 $aCarbone$xComposés.$2ram
655 4 $aOnline resources.
655 4 $aElectronic books.
700 1 $aMeijere, A. de.
710 2 $aLINK (Online service)
776 08 $iPrint version:$tCarbon Rich compounds I.$dBerlin ; New York : Springer, ©1998$z3540641106$w(OCoLC)39907465
830 0 $aTopics in current chemistry ;$v196.$x0340-1022
856 40 $3Google$uhttp://books.google.com/books?id=8HgvAQAAIAAJ
856 40 $3OhioLINK$uhttp://rave.ohiolink.edu/ebooks/ebc/3540696911
856 40 $3OhioLINK$uhttp://rave.ohiolink.edu/ebooks/ebc/3540494510
856 40 $3SpringerLink$uhttps://doi.org/10.1007/3-540-69691-1
856 40 $uhttp://uclibs.org/PID/5926
856 40 $uhttp://books.eclibrary.ca/isbn/9783540696919$zAccess restricted to Harris Learning Library use, and to students, faculty, and staff of Nipissing University.
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029 1 $aNZ1$b14997341
029 1 $aNZ1$b15297389
029 1 $aAU@$b000065097802
994 $aZ0$bIME
948 $hNO HOLDINGS IN IME - 126 OTHER HOLDINGS