Unconventional bifunctional Lewis-Brønsted acid activation mode in bicyclic guanidine-catalyzed conjugate addition reactions
10.3390/molecules200815108
Saved in:
Main Authors: | Cho, B, Wong, M.W |
---|---|
Other Authors: | DEPT OF CHEMISTRY |
Format: | Article |
Published: |
MDPI AG
2020
|
Subjects: | |
Online Access: | https://scholarbank.nus.edu.sg/handle/10635/179653 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Institution: | National University of Singapore |
Similar Items
-
N-HETEROCYCLIC CARBENE AND ISOTHIOUREA CATALYSIS: FROM ACYLATION CHEMISTRY TO HETEROCYCLE SYNTHESIS
by: ONG JUN YANG
Published: (2020) -
Chiral bicyclic guanidine as a versatile brønsted base catalyst for the enantioselective michael reactions of dithiomalonates and β-keto thioesters
by: Ye, W., et al.
Published: (2011) -
Chiral bicyclic guanidine as a versatile brønsted base catalyst for the enantioselective michael reactions of dithiomalonates and β-keto thioesters
by: Ye, W., et al.
Published: (2014) -
Chiral bicyclic guanidine as a versatile brønsted base catalyst for the enantioselective michael reactions of dithiomalonates and β-keto thioesters
by: Ye, W., et al.
Published: (2014) -
Efficient Lewis acid-assisted Brønsted acid (LBA) catalysis in the iron-catalyzed Friedel-Crafts alkylation reaction of indoles
by: Jiang, Z.-Y., et al.
Published: (2014)