Science of Synthesis: Stereoselective Synthesis Vol. 1 (eBook, PDF)

Stereoselective Reactions of Carbon-Carbon Double Bonds

• Format: PDF

Produktbeschreibung

C=C reactions are highly attractive as they are additions, and thus by nature highly atom-economic. Specific topics discussed: stereoselective addition of one or more carbon or heteroatom groups across a C=C bond (e.g., dihydroxylation, hydroboration, hydroamination, conjugate addition), epoxidation, aziridination, and cyclopropanation.

This volume is part of a 3-volume set: Science of Synthesis Stereoselective Synthesis Workbench Edition

Further information about Stereoselective Synthesis (including sample pages and the table of contents)

Produktdetails

• Verlag: Thieme
• Seitenzahl: 1056
• Erscheinungstermin: 14. Mai 2014
• Englisch
• ISBN-13: 9783131789211
• Artikelnr.: 40839059

Inhaltsangabe

<p>1.1 Dihydroxylation, Aminohydroxylation, Diamination, and Dibromination of Carbon&#8212;Carbon Double Bonds<br>1.2 Epoxidation of Carbon&#8212;Carbon Double Bonds<br>1.3 Epoxidation of Enones by Nucleophilic Oxidation<br>1.4 Aziridination<br>1.5 Hydrogenation of Carbon&#8212;Carbon Double Bonds<br>1.6 Hydrogenation of Arenes and Hetarenes<br>1.7 Stereoselective Hydroboration and Diboration of Carbon&#8212;Carbon Double Bonds<br>1.8 Carbometalation of Carbon&#8212;Carbon Double Bonds<br>1.9 Hydroformylation, Hydrocarbonylation, Hydrocyanation, and Hydroacylation of Carbon&#8212;Carbon Double Bonds<br>1.10 Hydrovinylation and Hydroarylation of Carbon&#8212;Carbon Double Bonds<br>1.11 Reductive Coupling and Cyclization of Carbon&#8212;Carbon Multiple Bonds<br>1.12 Conjugate Addition Reactions<br>1.13 Hydroamination, Hydrophosphination, Hydrophosphinylation, and Hydrophosphonylation of Carbon&#8212;Carbon Double Bonds<br>1.14 Cyclopropanation Reactions<br>1.15 Enantioselective and Diastereoselective Alkene Metathesis<br>1.16 Addition of Free Radicals to Carbon&#8212;Carbon Multiple Bonds<br>1.17 Asymmetric Hydrosilylation of Carbon&#8212;Carbon Double Bonds</p>