| Record ID | harvard_bibliographic_metadata/ab.bib.12.20150123.full.mrc:276694216:1453 |
| Source | harvard_bibliographic_metadata |
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LEADER: 01453cam a2200337 a 4500
001 012257162-2
005 20100430091411.0
008 090706s2009 gw a b 001 0 eng
015 $aGBA968239$2bnb
016 7 $a015305568$2Uk
020 $a9783527323807
020 $a3527323805
020 $a9783527626984
020 $a3527626980
035 0 $aocn406176490
040 $aUKM$cUKM$dBTCTA$dBWX$dOCLCQ$dOHX$dCDX
042 $aukblsr
050 4 $aQD281.A5$bC38 2009
082 04 $a547.2$222
245 00 $aCatalytic asymmetric Friedel-Crafts alkylations /$cedited by Marco Bandini and Achille Umani-Ronchi ; with a foreword by George A. Olah.
260 $aWeinheim :$bWiley-VCH,$cc2009.
300 $axvi, 301 p. :$bill. ;$c25 cm.
504 $aIncludes bibliographical references and index.
505 0 $aGeneral aspects and historical background -- Michael addition -- Addition to carbonyl compounds -- Nucleophilic allylic alkylation and hydroarylation of allenes -- Nucleophilic substitution on Csp³ carbon atoms -- Unactivated alkenes -- Catalytic asymmetric Friedel-Crafts alkylations in total synthesis -- Industrial Friedel-Crafts chemistry.
650 0 $aFriedel-Crafts reaction.
700 1 $aBandini, Marco.
700 1 $aUmani-Ronchi, Achille.
776 08 $iOnline version:$tCatalytic asymmetric Friedel-Crafts alkylations.$dWeinheim : Wiley-VCH, ©2009$w(OCoLC)625410206
988 $a20100329
049 $aHLSS
906 $0OCLC