Synfacts 2013; 9(1): 0102
DOI: 10.1055/s-0032-1317904
Organo- and Biocatalysis
© Georg Thieme Verlag Stuttgart · New York

Thiourea-Assisted Iminium Catalysis

Contributor(s):
Benjamin List
,
Ji Hye Kim
Wang Y, Yu T.-Y, Zhang H.-B, Luo Y.-C, Xu P.-F * Lanzhou University, P. R. of China
Hydrogen-Bond-Mediated Supramolecular Iminium Ion Catalysis.

Angew. Chem. Int. Ed. 2012;
51: 12339-12342
Further Information

Publication History

Publication Date:
17 December 2012 (online)

 

Significance

A thiourea-assisted iminium catalysis has been described. It was found that simple thioureas accelerate previously established reactions of α,β-unsaturated aldehydes with MacMillan’s organocatalyst, presumably by binding to the counteranion of the iminium intermediate. The use of chiral thioureas did not have a significant effect on the enantioselectivity.


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Comment

The profound influence of anions on reactivity and selectivity in asymmetric iminium ­catalysis is well established (S. Mayer, B. List ­Angew. Chem. Int. Ed. 2006, 45, 4193). Therefore, thioureas could be expected to influence the activity and selectivity by anion binding during the catalysis (see Review below). In the current report, a mild positive influence of thioureas on reactivity is demonstrated. Development of a chiral thiourea as the only source of asymmetric information remains as the true challenge of this approach.


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Review

Z. Zhang, P. R. Schreiner Chem. Soc. Rev. 2009, 38, 1187–1198.


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