Enantioselective epoxidation of protected allylic and homoallylic amines via chiral cationic ion-pairing catalysis
Asymmetric epoxidation is one of the most versatile organic transformations as up to two stereogenic centre can be generated from the three member oxirane product in a single step. Although numerous reports on catalytic asymmetric epoxidation on allylic alcohols had been published in the literature...
Saved in:
Main Author: | Chin, Kek Foo |
---|---|
Other Authors: | Tan Choon Hong |
Format: | Thesis-Doctor of Philosophy |
Language: | English |
Published: |
Nanyang Technological University
2018
|
Subjects: | |
Online Access: | http://hdl.handle.net/10356/75402 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Institution: | Nanyang Technological University |
Language: | English |
Similar Items
-
Enantioselective Steglich rearrangement catalysed by chiral guanidinium ion pairs
by: Yang, Ziqi
Published: (2023) -
Enantioselective addition-alkylation reactions via bisguanidinium silicate ion pair catalysis
by: Chen, Wen Chao
Published: (2020) -
A chiral pentanidium and pyridinyl-sulphonamide ion pair as an enantioselective organocatalyst for Steglich rearrangement
by: Yang, Ziqi, et al.
Published: (2024) -
The first example of enantioselective allyl transfer from a linear homoallylic alcohol to an aldehyde
by: Loh, T.-P., et al.
Published: (2014) -
Syntheses of enantioenriched homoallylic hydroxylamines and ß-lactams using sugar template as the chiral auxiliary.
by: Wong, Shwo Mun.
Published: (2011)