|
|
|
|
LEADER |
04216nam a22004815i 4500 |
001 |
978-3-642-34286-8 |
003 |
DE-He213 |
005 |
20151111061303.0 |
007 |
cr nn 008mamaa |
008 |
121031s2013 gw | s |||| 0|eng d |
020 |
|
|
|a 9783642342868
|9 978-3-642-34286-8
|
024 |
7 |
|
|a 10.1007/978-3-642-34286-8
|2 doi
|
040 |
|
|
|d GrThAP
|
050 |
|
4 |
|a QD410-412.5
|
072 |
|
7 |
|a PNND
|2 bicssc
|
072 |
|
7 |
|a SCI013040
|2 bisacsh
|
082 |
0 |
4 |
|a 547.05
|2 23
|
245 |
1 |
0 |
|a Inventing Reactions
|h [electronic resource] /
|c edited by Lukas J. Gooßen.
|
264 |
|
1 |
|a Berlin, Heidelberg :
|b Springer Berlin Heidelberg :
|b Imprint: Springer,
|c 2013.
|
300 |
|
|
|a XIV, 342 p.
|b online resource.
|
336 |
|
|
|a text
|b txt
|2 rdacontent
|
337 |
|
|
|a computer
|b c
|2 rdamedia
|
338 |
|
|
|a online resource
|b cr
|2 rdacarrier
|
347 |
|
|
|a text file
|b PDF
|2 rda
|
490 |
1 |
|
|a Topics in Organometallic Chemistry,
|x 1436-6002 ;
|v 44
|
505 |
0 |
|
|a Barry Trost: Transition metal catalyzed allylic alkylation -- Jeffrey W. Bode: Reinventing Amide Bond Formation -- Naoto Chatani and Mamoru Tobisu: Catalytic Transformations Involving the Cleavage of C-OMe Bonds -- Gregory L. Beutner and Scott E. Denmark: The Interplay of Invention, Observation and Discovery in the Development of Lewis Base Activation of Lewis Acids for Catalytic Enantioselective Synthesis -- David R. Stuart and Keith Fagnou: The Discovery and Development of a Palladium(II)-Catalyzed Oxidative Cross-Coupling of Two Unactivated Arenes -- Lukas Gooßen and Käthe Gooßen: Decarboxylative Cross-Coupling Reactions -- A. Stephen K. Hashmi: Gold-Catalyzed Organic Reactions -- Ben List: Developing Catalytic Asymmetric Acetalizations -- Steven M. Bischof, Brian G. Hashiguchi, Michael M. Konnick, and Roy A. Periana: The De NovoDesign of CH Bond Hydroxylation Catalysts -- Benoit Cardinal-David, Karl A. Scheidt: Carbene Catalysis: Beyond the Benzoin and Stetter Reactions -- Kenso Soai and Tsuneomi Kawasaki: Asymmetric autocatalysis of pyrimidyl alkanol -- Douglas C. Behenna and Brian M. Stoltz: Natural Products as Inspiration for Reaction Development: Catalytic Enantioselective Decarboxylative Reactions of Prochiral Enolate Equivalents. Hisashi Yamamoto: Acid Catalysis in Organic Synthesis.
|
520 |
|
|
|a Barry Trost: Transition metal catalyzed allylic alkylation.- Jeffrey W. Bode: Reinventing Amide Bond Formation.- Naoto Chatani and Mamoru Tobisu: Catalytic Transformations Involving the Cleavage of C-OMe Bonds.- Gregory L. Beutner and Scott E. Denmark: The Interplay of Invention, Observation and Discovery in the Development of Lewis Base Activation of Lewis Acids for Catalytic Enantioselective Synthesis.- David R. Stuart and Keith Fagnou: The Discovery and Development of a Palladium(II)-Catalyzed Oxidative Cross-Coupling of Two Unactivated Arenes.- Lukas Gooßen and Käthe Gooßen: Decarboxylative Cross-Coupling Reactions.- A. Stephen K. Hashmi: Gold-Catalyzed Organic Reactions.- Ben List: Developing Catalytic Asymmetric Acetalizations.- Steven M. Bischof, Brian G. Hashiguchi, Michael M. Konnick, and Roy A. Periana: The De NovoDesign of CH Bond Hydroxylation Catalysts.- Benoit Cardinal-David, Karl A. Scheidt: Carbene Catalysis: Beyond the Benzoin and Stetter Reactions.- Kenso Soai and Tsuneomi Kawasaki: Asymmetric autocatalysis of pyrimidyl alkanol.- Douglas C. Behenna and Brian M. Stoltz: Natural Products as Inspiration for Reaction Development: Catalytic Enantioselective Decarboxylative Reactions of Prochiral Enolate Equivalents. Hisashi Yamamoto: Acid Catalysis in Organic Synthesis.
|
650 |
|
0 |
|a Chemistry.
|
650 |
|
0 |
|a Organic chemistry.
|
650 |
|
0 |
|a Organometallic chemistry.
|
650 |
|
0 |
|a Catalysis.
|
650 |
1 |
4 |
|a Chemistry.
|
650 |
2 |
4 |
|a Organometallic Chemistry.
|
650 |
2 |
4 |
|a Catalysis.
|
650 |
2 |
4 |
|a Organic Chemistry.
|
700 |
1 |
|
|a Gooßen, Lukas J.
|e editor.
|
710 |
2 |
|
|a SpringerLink (Online service)
|
773 |
0 |
|
|t Springer eBooks
|
776 |
0 |
8 |
|i Printed edition:
|z 9783642342851
|
830 |
|
0 |
|a Topics in Organometallic Chemistry,
|x 1436-6002 ;
|v 44
|
856 |
4 |
0 |
|u http://dx.doi.org/10.1007/978-3-642-34286-8
|z Full Text via HEAL-Link
|
912 |
|
|
|a ZDB-2-CMS
|
950 |
|
|
|a Chemistry and Materials Science (Springer-11644)
|