Cu(I)-catalyzed asymmetric diamination of conjugated dienes
- PMID: 18763785
- PMCID: PMC2659555
- DOI: 10.1021/ol801605w
Cu(I)-catalyzed asymmetric diamination of conjugated dienes
Abstract
A Cu(I)-catalyzed asymmetric diamination for a variety of conjugated dienes and a triene with encouraging ee's has been effectively achieved using (R)-DTBM-SEGPHOS as a chiral ligand and di- tert-butyldiaziridinone as the nitrogen source.
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For recent Cu(II)-mediated intramolecular diamination, see: Zabawa TP, Kasi D, Chemler SR. J. Am. Chem. Soc. 2005;127:11250. Zabawa TP, Chemler SR. Org. Lett. 2007;9:2035.
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For Rh(II)-, Fe(III)-catalyzed diamination with TsNCl2, see: Li G, Wei H-X, Kim SH, Carducci MD. Angew. Chem., Int. Ed. 2001;40:4277. Wei H-X, Kim SH, Li G. J. Org. Chem. 2002;67:4777.
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For a recent Pd(II)-catalyzed intermolecular diamination of conjugated dienes, see: Bar GLJ, Lloyd-Jones GC, Booker-Milburn KI. J. Am. Chem. Soc. 2005;127:7308.
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