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Australian Journal of Chemistry Australian Journal of Chemistry Society
An international journal for chemical science
RESEARCH ARTICLE

The Discovery of Catalytic Enantioselective Polyvalent Iodine Mediated Reactions

Marsewi Ngatimin A and David W. Lupton A B
+ Author Affiliations
- Author Affiliations

A School of Chemistry, Monash University, Clayton Campus, Vic. 3800, Australia.

B Corresponding author. Email: david.lupton@sci.monash.edu.au

Australian Journal of Chemistry 63(4) 653-658 https://doi.org/10.1071/CH09625
Submitted: 3 December 2009  Accepted: 3 February 2010   Published: 8 April 2010

Abstract

The use of polyvalent iodine mediated reactions for the synthesis of enantiopure materials has developed into an active field of research. Recently, new chiral aryl iodides, and conditions for their substoichiometric use, have allowed catalytic variants to be achieved. This highlight draws attention to recent discoveries in this emerging field.


Acknowledgement

We acknowledge financial support of the ARC (DP0881137) and Roche (Palo Alto) through donation of equipment and Monash University through an ECR program. We also wish to acknowledge valuable contributions made by the referees regarding an earlier version of this manuscript.


References


[1]   D. W. C. MacMillan, Nature 2008, 455,  304.
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        | Crossref |  GoogleScholarGoogle Scholar | CAS |  
        | Crossref |  GoogleScholarGoogle Scholar | CAS |  
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        | Crossref |  GoogleScholarGoogle Scholar | CAS |  
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        | Crossref |  GoogleScholarGoogle Scholar | CAS |  
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        | Crossref |  GoogleScholarGoogle Scholar | CAS |  
        | Crossref |  GoogleScholarGoogle Scholar | CAS |  
        | Crossref |  GoogleScholarGoogle Scholar | CAS |  
        | Crossref |  GoogleScholarGoogle Scholar | CAS |  
        | Crossref |  GoogleScholarGoogle Scholar | CAS |  
         
        | Crossref |  GoogleScholarGoogle Scholar | CAS |  
         
        |  CAS |  
        | Crossref |  GoogleScholarGoogle Scholar | CAS |  
        | Crossref |  GoogleScholarGoogle Scholar | CAS |  
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