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Enantioselective conjugate addition with chiral amidocuprates

โœ 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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โœฆ 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


๐Ÿ“œ SIMILAR VOLUMES


Enantioselective Conjugate Additions
โœ Mukund P. Sibi; Shankar Manyem ๐Ÿ“‚ Article ๐Ÿ“… 2000 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 586 KB
Enantioselective Copper-Catalysed Conjug
โœ Alexandre Alexakis; Cyril Benhaim ๐Ÿ“‚ Article ๐Ÿ“… 2002 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 449 KB

The review covers the efforts made over the last decade towards designing efficient copper-catalysed systems for the asymmetric conjugate addition reaction.