Organocatalyzed Asymmetric α-Oxidation, α-Aminoxylation and α-Amination of Carbonyl Compounds 英文参考文献.docVIP
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Organocatalyzed Asymmetric α-Oxidation, α-Aminoxylation and α-Amination of Carbonyl Compounds 英文参考文献
Molecules 2010, 15, 917-958; doi:10.3390/moleculeOPEN ACCESS
molecules
ISSN 1420-3049
/journal/molecules
Review
Organocatalyzed Asymmetric ?-Oxidation, ?-Aminoxylation
and ?-Amination of Carbonyl Compounds
Tirayut Vilaivan * and Worawan Bhanthumnavin
Organic Synthesis Research Unit, Department of Chemistry, Faculty of Science, Chulalongkorn
University, Phayathai Road, Patumwan, Bangkok 10330, Thailand;
E-Mail: worawan.b@chula.ac.th (W.B.)
* Author to whom correspondence should be addressed; E-Mail: vtirayut@chula.ac.th.
Received: 25 December 2009; in revised form: 27 January 2010 / Accepted: 5 February 2010 /
Published: 11 Februray 2010
Abstract: Organocatalytic asymmetric ?-oxidation and amination reactions of carbonyl
compounds are highly useful synthetic methodologies, especially in generating chiral
building blocks that previously have not been easily accessible by traditional methods. The
concept is relatively new and therefore the list of new catalysts, oxidizing and aminating
reagents, as well as new substrates, are expanding at an amazing rate. The scope of this
review includes new reactions and catalysts, mechanistic aspects and synthetic applications
of ?-oxidation, hydroxylation, aminoxylation, amination, hydrazination, hydroxyamination
and related ?-heteroatom functionalization of aldehydes, ketones and related active
methylene compounds published during 2005–2009.
Keywords: organocatalyst; chiral catalyst; ?-oxidation; ?-amination; ?-aminoxylation;
nitrosoaldol reaction; aldehyde; ketone; active methylene compound
Outline
1. Introduction
2. ?-Amination reactions
2.1. ?-Amination with azodicarboxylate esters
2.1.1 Simple aldehydes and ketones
2.1.2 Other carbonyl substrates
Molecules 2010, 15
918
2.1.3. Applications
2.2. ?-Sulfamidation
2.3. ?-Hydroxyamination
3. ?-Aminoxylation reactions
3.1. ?-Aminoxylation with nitrosobenzene
3.1.1. Substrates
3.1.2. Catalysts
3.1.3. Applications
3.1.4. Am
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