Science of Synthesis: Stereoselective Synthesis Vol. 2

Science of Synthesis: Stereoselective Synthesis Vol. 2
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Stereoselective Reactions of Carbonyl and Imino Groups, Wissenschaftler
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Artikel-Nr:
9783131789419
Veröffentl:
2014
Seiten:
1052
Autor:
Gary A. Molander
Serie:
Science of Synthesis
eBook Typ:
PDF
eBook Format:
Reflowable
Kopierschutz:
Digital Watermark [Social-DRM]
Sprache:
Englisch
Beschreibung:

In Science of Synthesis: Stereoselective Synthesis expert authors present the best and most reliable methods currently available for the preparation of nonra-cemic compounds. These methods may be stoichiometric or catalytic, and the latter may include metal, organ ic, or enzyme catalysis. The three volumes of Stereoselective Synthesis provide ...

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.

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)

<p>2.1 Reduction of Carbonyl Groups: Hydrogenation<br>2.2 Reduction of Carbonyl Groups: Transfer Hydrogenation, Hydrosilylation, Catalytic Hydroboration, and Reduction with Borohydrides, Aluminum Hydrides, or Boranes<br>2.3 Enzymatic Reduction of Carbonyl Groups<br>2.4 Oxidative Deracemization<br>2.5 Stereoselective Reduction of Imino Groups<br>2.6 Epoxidation and Aziridination of Carbonyl Groups and Imines<br>2.7 Alkylation of Carbonyl and Imino Groups<br>2.8 Allylation of Carbonyl and Imino Groups<br>2.9 Arylation and Alkenylation of Carbonyl and Imino Groups<br>2.10.1 Enantioselective Addition of Acetylide Nucleophiles to Carbonyl Compounds<br>2.10.2 Enantioselective Addition of Metal Alkynylides to Imino Groups<br>2.11 Hydrocyanation, Cyanosilylation, and Hydrophosphonylation of Carbonyl and Imino Groups<br>2.12 Asymmetric Mukaiyama Aldol Reaction<br>2.13 Direct Aldol Reactions<br>2.14 Enzymatic Direct Aldol Additions<br>2.15 Asymmetric Morita&#8211;Baylis&#8211;Hillman Reaction and Its Aza Analogue<br>2.16 Mannich Reaction<br>2.17 Asymmetric Benzoin and Stetter Reactions<br>2.18 Asymmetric Synthesis of Spiroketals, Bisspiroketals, and Spiroaminals</p>

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