MARC Record from Library of Congress

LEADER: 02150cam a22003018i 4500
001 2015013578
003 DLC
005 20150501092227.0
008 150422s2015 nju b 001 0 eng c
010 $a 2015013578
020 $a9781118347966 (cloth)
040 $aWaSeSS/DLC$beng$cWaSeSS$erda
042 $apcc
050 00 $aQD281.R35$bM65 2015
082 00 $a547/.2$223
245 00 $aMolecular rearrangements in organic synthesis /$cEdited by Christian M. Rojas.
263 $a1510
264 1 $aHoboken, New Jersey :$bJohn Wiley & Sons, Inc.,$c2015.
300 $apages cm
336 $atext$2rdacontent
337 $aunmediated$2rdamedia
338 $avolume$2rdacarrier
504 $aIncludes bibliographical references and index.
505 0 $a1,2-migrations. Pinacol and semi-pinacol rearrangements in total synthesis -- Baeyer-Villiger (BV) oxidation/rearrangement in organic synthesis -- The Wolff rearrangement : tactics, strategies and recent applications in organic synthesis -- Alkyl and acyl azide rearrangements -- Beckmann rearrangements and fragmentations in organic synthesis -- Brook rearrangement. 1,2-migrations via three-membered rings. The quasi-favorskii rearrangement -- The Ramberg-Backlund reaction -- Applications of di-pi-methane and related rearrangement reactions in chemical synthesis. 1,3-transpositions. Payne rearrangement -- Vinylcyclopropane-cyclopentene rearrangement -- Ferrier carbocyclization reaction. [3,3]- and [2,3]-sigmatropic rearrangements. The Claisen rearrangement -- [3,3]-sigmatropic rearrangements with heteroatom-heteroatom bonds -- [2,3]-rearrangements of ammonium zwitterions -- Oxonium ylide rearrangements in synthesis -- The [2,3]-Wittig rearrangement -- The Mislow-Evans rearrangement. Ipso rearrangements. Smiles rearrangements -- Pummerer-type reactions as powerful tools in organic synthesis.
650 0 $aRearrangements (Chemistry)
650 0 $aOrganic compounds$xSynthesis.
700 1 $aRojas, Christian Miguel,$eeditor.
776 08 $iOnline version:$tMolecular rearrangements in organic synthesis$dHoboken, New Jersey : John Wiley & Sons, Inc., 2015$z9781118939888$w(DLC) 2015017259