Highly efficient assembly of 3-hydroxy oxindole scaffold via a catalytic decarboxylative [1,2]-addition strategy
10.1021/cs300628w
Saved in:
Main Authors: | Ren, Q., Huang, J., Wang, L., Li, W., Liu, H., Jiang, X., Wang, J. |
---|---|
Other Authors: | CHEMISTRY |
Format: | Article |
Published: |
2014
|
Subjects: | |
Online Access: | http://scholarbank.nus.edu.sg/handle/10635/52976 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Institution: | National University of Singapore |
Similar Items
-
Catalytic and enantioselective α-functionalization of oxindoles through oxidative reactions with naphthoquinones
by: Siau, W.-Y., et al.
Published: (2014) -
Catalytic and enantioselective α-functionalization of oxindoles through oxidative reactions with naphthoquinones
by: Siau, W.-Y., et al.
Published: (2014) -
Asymmetric organocatalytic decarboxylative Mannich reaction using β-keto acids: A new protocol for the synthesis of chiral â-amino ketones
by: Jiang, C., et al.
Published: (2014) -
Asymmetric organocatalytic decarboxylative Mannich reaction using β-keto acids: A new protocol for the synthesis of chiral â-amino ketones
by: Jiang, C., et al.
Published: (2014) -
Diastereodivergent synthesis of 3-spirocyclopropyl-2-oxindoles through direct enantioselective cyclopropanation of oxindoles
by: Dou, X., et al.
Published: (2014)