Palladium/N-heterocyclic carbene catalysed regio and diastereoselective reaction of ketones with allyl reagents via inner-sphere mechanism
Palladium catalyzed allylic substitution reactions typically proceed via an outer sphere mechanism, yielding predominately linear products. Here, the authors report an inner sphere process for the allylic substitution of ketone enolates, giving branched products with up to three contiguous stereocen...
Saved in:
Main Authors: | Da-Chang Bai, Fei-Le Yu, Wan-Ying Wang, Di Chen, Hao Li, Qing-Rong Liu, Chang-Hua Ding, Bo Chen, Xue-Long Hou |
---|---|
Format: | article |
Language: | EN |
Published: |
Nature Portfolio
2016
|
Subjects: | |
Online Access: | https://doaj.org/article/a2190ea2df8449c6b683e64e74797d1d |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Regio- and enantioselective umpolung gem-difluoroallylation of hydrazones via palladium catalysis enabled by N-heterocyclic carbene ligand
by: Shuai Huang, et al.
Published: (2021) -
Palladium-catalyzed regio- and enantioselective migratory allylic C(sp3)-H functionalization
by: Ye-Wei Chen, et al.
Published: (2021) -
Asymmetric Suzuki-Miyaura coupling of heterocycles via Rhodium-catalysed allylic arylation of racemates
by: Philipp Schäfer, et al.
Published: (2017) -
Chromoselective access to Z- or E- allylated amines and heterocycles by a photocatalytic allylation reaction
by: Ana María Martínez-Gualda, et al.
Published: (2019) -
Correction: Author Correction: Asymmetric Suzuki-Miyaura coupling of heterocycles via Rhodium-catalysed allylic arylation of racemates
by: Philipp Schäfer, et al.
Published: (2018)