Diastereoselective intramolecular hydride transfer triggered by electrophilic halogenation of aryl alkenes
Diastereoselective hydride transfer could be triggered by electrophilic halogenation (bromination or fluorination) of homoallylic alcohol O-Bn ethers. The resulting diastereomerically enriched haloalkyl alcohols underwent subsequent intramolecular nucleophilic substitution to afford the correspondin...
Saved in:
Main Authors: | Wang, Bin, Gandamana, Dhika Aditya, León Rayo, David Fabian, Gagosz, Fabien, Chiba, Shunsuke |
---|---|
Other Authors: | School of Physical and Mathematical Sciences |
Format: | Article |
Language: | English |
Published: |
2022
|
Subjects: | |
Online Access: | https://hdl.handle.net/10356/154839 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Institution: | Nanyang Technological University |
Language: | English |
Similar Items
-
Diastereoselective hydroalkylation of aryl alkenes enabled by remote hydride transfer
by: Gandamana, Dhika Aditya, et al.
Published: (2021) -
Diastereoselective intramolecular hydride transfer under brønsted acid catalysis
by: Wang, Bin, et al.
Published: (2020) -
Diastereoselective intramolecular hydride transfer
by: Gandamana, Dhika Aditya
Published: (2021) -
Photoinduced cross-coupling of aryl Iodides with alkenes
by: Liu, Yuliang, et al.
Published: (2022) -
Alkyl ethers as traceless hydride donors in brønsted acid catalyzed intramolecular hydrogen atom transfer
by: Gandamana, Dhika Aditya, et al.
Published: (2019)