Enantioselective conjugate addition with chiral amidocuprates
โ Scribed by Bryant E. Rossiter; Masakatsu Eguchi
- Book ID
- 104226506
- Publisher
- Elsevier Science
- Year
- 1990
- Tongue
- French
- Weight
- 269 KB
- Volume
- 31
- Category
- Article
- ISSN
- 0040-4039
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โฆ Synopsis
A series of chii secondary amines have been screened as non-tmnsfearable cuprate ligands for the promotion of enantiosekctivity in conjugate addition to 2cyclohexenone.
A mechanism is presented to rationalize the enantioselectivity obsaved.
Conjugate addition to enones using organocuprate reagents1 is a useful organic reaction whose utility would be extended if it were rendered enantioselective. A number of chiral organocuprates have been developed to do such, some with considerable success. 2-5 Little is known, however, about the relationship in these reactions
๐ SIMILAR VOLUMES
The review covers the efforts made over the last decade towards designing efficient copper-catalysed systems for the asymmetric conjugate addition reaction.