Cu-catalyzed asymmetric addition of sp2-hybridized zirconium nucleophiles to racemic allyl bromides
Alkenylzirconium nucleophiles made in situ by the hydrozirconation of terminal alkynes undergo dynamic kinetic asymmetric allylic alkenylation with racemic allyl bromides to give enantioenriched products.
Main Authors: | Sidera, M, Fletcher, S |
---|---|
格式: | Journal article |
語言: | English |
出版: |
Royal Society of Chemistry
2015
|
相似書籍
-
Cu-catalyzed asymmetric addition of sp²-hybridized zirconium nucleophiles to racemic allyl bromides.
由: Sidera, M, et al.
出版: (2015) -
Asymmetric cross-coupling of alkyl, alkenyl and (hetero)aryl nucleophiles with racemic allyl halides
由: Schafer, P, et al.
出版: (2017) -
Mechanistic studies on a Cu-catalyzed asymmetric allylic al-kylation with cyclic racemic starting materials
由: Rideau, E, et al.
出版: (2017) -
Non-stabilized nucleophiles in Cu-catalysed dynamic kinetic asymmetric allylic alkylation
由: You, H, et al.
出版: (2015) -
Rhodium-catalysed asymmetric allylic arylation of racemic halides with arylboronic acids
由: Sidera, M, et al.
出版: (2015)