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Synthesis 2014; 46(10): 1311-1320
DOI: 10.1055/s-0033-1338602
DOI: 10.1055/s-0033-1338602
special topic
Tandem Regioselective Rhodium-Catalyzed Hydroformylation–Enantioselective Aminocatalytic anti-Mannich Reaction
Further Information
Publication History
Received: 13 January 2014
Accepted: 08 February 2014
Publication Date:
26 March 2014 (online)

Abstract
The first tandem regioselective hydroformylation and enantioselective organocatalytic anti-Mannich reaction is reported. Starting from α-olefins, valuable functionalized amino acid derivatives were obtained in excellent yields and with high levels of diastereo- and enantioselectivities. The products represent valuable building blocks for biologically and pharmaceutically interesting targets.
Key words
tandem reactions - asymmetric synthesis - homogeneous catalysis - organocatalysis - hydroformylationSupporting Information
- for this article is available online at http://www.thieme-connect.com/ejournals/toc/synthesis. Included are further experimental descriptions, determination of enantiomeric excess, and spectroscopic and analytical data.
- Supporting Information
-
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For recent examples, see:
For reviews on organocatalysis of the Mannich reaction, see:
For other tandem reactions applying hydroformylation as the initial step, see: