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MARC Record from marc_columbia

Record ID marc_columbia/Columbia-extract-20221130-004.mrc:445926962:2950
Source marc_columbia
Download Link /show-records/marc_columbia/Columbia-extract-20221130-004.mrc:445926962:2950?format=raw

LEADER: 02950mam a2200313 a 4500
001 1848713
005 20220609010547.0
008 960827t19961996enk b 001 0 eng d
020 $a0126769451
035 $a(OCoLC)ocm35308903
035 $9ALT3318CU
035 $a(NNC)1848713
035 $a1848713
040 $aWSU$cWSU$dOrLoB-B
100 1 $aSundberg, Richard J.,$d1938-$0http://id.loc.gov/authorities/names/n83057554
245 10 $aIndoles /$cR.J. Sundberg.
260 $aLondon ;$aSan Diego :$bAcademic Press,$c[1996], ©1996.
300 $axv, 175 pages ;$c24 cm.
336 $atext$btxt$2rdacontent
337 $aunmediated$bn$2rdamedia
490 1 $aBest synthetic methods. Key systems and functional groups
504 $aIncludes bibliographical references and index.
505 00 $gCh. 1.$tIntroduction --$gCh. 2.$tCategory Ia Cyclizations --$gCh. 3.$tCategory Ib Cyclizations --$gCh. 4.$tCategory Ic Cyclizations --$gCh. 5.$tCategory Ii Cyclizations --$gCh. 6.$tCategory IIab Cyclizations --$gCh. 7.$tCategory IIac Cyclizations --$gCh. 8.$tIndoles by Annelation of Pyrroles --$gCh. 9.$tSynthetic Modification of Indoles by Substitution at Nitrogen --$gCh. 10.$tIntroduction of Substituents at C2 --$gCh. 11.$tIntroduction of Substituents at C3 --$gCh. 12.$tModification of 3-Alkyl Substituents by Nucleophilic Substitution --$gCh. 13.$tIntroduction of the Tryptamine and Tryptophan Side-Chains --$gCh. 14.$tIntroduction to Substituents on the Carbocyclic Ring --$gCh. 15.$tSelective Reduction and Oxidation Reactions --$gCh. 16.$tSynthetic Elaboration of Indole Derivatives using Cycloaddition Reactions.
520 $aIndoles continue to be of great interest to the pharmaceutical industry and at the current time several thousand specific new derivatives are reported annually. Research has been driven by the wide range of indole derivatives which occur in nature and by the biological activity of many indole derivatives, of both natural and synthetic origin.
520 8 $aThis book provides a systematic guide to the most useful and important reactions in the field for both synthesis and synthetic modification of the indole ring. While including the most recently developed and promising methods, it also updates information available on classical methods to give the reader an up-to-date and comprehensive view of the subject.
520 8 $aThe methods are illustrated by procedures drawn from the literature and by tables including examples chosen to indicate both the scope of applicability and variations in methodology. The organisation of the book is based on the retrosynthetic concept of identifying the bond(s) formed in the reaction, which in turn identifies potential starting materials.
650 0 $aIndole.$0http://id.loc.gov/authorities/subjects/sh85065725
830 0 $aBest synthetic methods.$pKey systems and functional groups.$0http://id.loc.gov/authorities/names/no96051558
852 00 $bsci$hQD401$i.I53 1996g