Details
Science of Synthesis: Stereoselective Synthesis Vol. 2
Stereoselective Reactions of Carbonyl and Imino Groups1. Auflage
259,99 € |
|
Verlag: | Thieme |
Format: | EPUB |
Veröffentl.: | 14.05.2014 |
ISBN/EAN: | 9783131789518 |
Sprache: | englisch |
Anzahl Seiten: | 1052 |
Dieses eBook enthält ein Wasserzeichen.
Beschreibungen
<p>Carbonyl and imino groups are two of the most integral functional groups employed in organic synthesis. Specific topics discussed: reduction, alkylation, alkenylation, and arylation of these groups, as well as asymmetric aldol, Mannich, and Morita-Bayliss-Hillman reactions.</p><p>This volume is part of a 3-volume set: <cite>Science of Synthesis <a href="http://www.thieme.com/index.php?page=shop.product_details&amp;flypage=flypage.tpl&amp;product_id=1313&amp;category_id=11&amp;keyword=3-volume+set&amp;option=com_virtuemart&amp;Itemid=53">Stereoselective Synthesis</a> Workbench Edition</cite><BR><br ><a href="http://www.thieme-chemistry.com/sss">Further information about Stereoselective Synthesis</a> (including sample pages and the table of contents)</p>
&lt;p&gt;2.1 Reduction of Carbonyl Groups: Hydrogenation&lt;br&gt;2.2 Reduction of Carbonyl Groups: Transfer Hydrogenation, Hydrosilylation, Catalytic Hydroboration, and Reduction with Borohydrides, Aluminum Hydrides, or Boranes&lt;br&gt;2.3 Enzymatic Reduction of Carbonyl Groups&lt;br&gt;2.4 Oxidative Deracemization&lt;br&gt;2.5 Stereoselective Reduction of Imino Groups&lt;br&gt;2.6 Epoxidation and Aziridination of Carbonyl Groups and Imines&lt;br&gt;2.7 Alkylation of Carbonyl and Imino Groups&lt;br&gt;2.8 Allylation of Carbonyl and Imino Groups&lt;br&gt;2.9 Arylation and Alkenylation of Carbonyl and Imino Groups&lt;br&gt;2.10.1 Enantioselective Addition of Acetylide Nucleophiles to Carbonyl Compounds&lt;br&gt;2.10.2 Enantioselective Addition of Metal Alkynylides to Imino Groups&lt;br&gt;2.11 Hydrocyanation, Cyanosilylation, and Hydrophosphonylation of Carbonyl and Imino Groups&lt;br&gt;2.12 Asymmetric Mukaiyama Aldol Reaction&lt;br&gt;2.13 Direct Aldol Reactions&lt;br&gt;2.14 Enzymatic Direct Aldol Additions&lt;br&gt;2.15 Asymmetric Morita&amp;#8211;Baylis&amp;#8211;Hillman Reaction and Its Aza Analogue&lt;br&gt;2.16 Mannich Reaction&lt;br&gt;2.17 Asymmetric Benzoin and Stetter Reactions&lt;br&gt;2.18 Asymmetric Synthesis of Spiroketals, Bisspiroketals, and Spiroaminals&lt;/p&gt;