How an early or late transition state impacts the stereoselectivity of tetrahydropyran formation by intramolecular oxa-Michael addition
The intramolecular oxa-Michael addition giving tetrahydropyrans has been examined experimentally using both acidic and basic catalysis. With acidic catalysis, the diequatorial product is exclusively obtained in a kinetically controlled reaction in all cases. Under basic conditions at low temperature...
Saved in:
Main Authors: | Csókás, Dániel, Ho, Annabel Xuan Ying, Ramabhadran, Raghunath O., Bates, Roderick Wayland |
---|---|
Other Authors: | School of Physical and Mathematical Sciences |
Format: | Article |
Language: | English |
Published: |
2020
|
Subjects: | |
Online Access: | https://hdl.handle.net/10356/141244 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Institution: | Nanyang Technological University |
Language: | English |
Similar Items
-
A synthesis of cyanolide A by intramolecular oxa-Michael addition
by: Bates, Roderick Wayland, et al.
Published: (2014) -
The intramolecular oxa-Michael reaction for tetrahydropyran formation : mechanism and synthesis
by: Csokas, Daniel
Published: (2019) -
The endo-aza-Michael addition in the synthesis of piperidines and pyrrolidines
by: Bates, Roderick Wayland, et al.
Published: (2020) -
Triple Michael addition reaction
by: Chatchai Thanupran
Published: (2023) -
Studies on the synthesis of tetrahydropyrans via oxa-Michael addition leading towards the total synthesis of Montanacin D
by: Ho, Annabel Xuan Ying
Published: (2021)