Synthesis and application to asymmetric allylic amination of substituted monodonor diazaphospholidine ligands
β Scribed by Christopher W Edwards; Mark R Shipton; Nathaniel W Alcock; Howard Clase; Martin Wills
- Book ID
- 104205632
- Publisher
- Elsevier Science
- Year
- 2003
- Tongue
- French
- Weight
- 214 KB
- Volume
- 59
- Category
- Article
- ISSN
- 0040-4020
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β¦ Synopsis
The synthesis of a series of substituted monodonor diazaphospholidine ligands is described. A regioselective lithiation process is a key step in one of these syntheses. The compounds are designed to be incorporated into soluble polymer and other solid phase supports. Enantiomeric excesses of up to 88% were observed when these compounds were employed in palladium-catalysed asymmetric amination reactions.
π SIMILAR VOLUMES
An efficient and flexible asymmetric synthesis of planar chiral ferrocenyl ligands bearing a stereogenic centre at the Ξ²-position to the metallocene backbone is described. A variety of donor groups can be independently introduced as electrophiles, thus allowing electronic and steric fine-tuning of t