BF₃-promoted reactions of α-amino acetals with alkynes to 2,5-disubstituted pyrroles
An efficient BF₃-promoted cyclization of α-amino acetals with alkynes for the assembly of substituted pyrroles has been developed. This cascade process uses easily accessible α-amino acetals as raw materials and can be achieved under mild conditions through a simple metal-free operation.
Saved in:
Main Authors: | Gao, Zhi-Yuan, He, Yu, Li, Lan-Yang, Tian, Jie-Sheng, Loh, Teck-Peng |
---|---|
Other Authors: | School of Physical and Mathematical Sciences |
Format: | Article |
Language: | English |
Published: |
2022
|
Subjects: | |
Online Access: | https://hdl.handle.net/10356/163494 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Institution: | Nanyang Technological University |
Language: | English |
Similar Items
-
Chemical synthesis of cyclotide from the medicinal plant clitoria ternatea
by: Wang, Yingqi
Published: (2013) -
Butelase-mediated cyclization and ligation of peptides and proteins
by: Qiu, Yibo, et al.
Published: (2016) -
Palladium-catalyzed one-pot highly regioselective 6-endo cyclization and alkylation of enynoates : synthesis of 2-alkanone pyrones
by: Tanveer Ahmad, et al.
Published: (2020) -
Desymmetrization of diolefinic diols by enantioselective amino-thiocarbamate-catalyzed bromoetherification: Synthesis of chiral spirocycles
by: Tay, D.W., et al.
Published: (2014) -
Nickel-Catalyzed Asymmetric Reductive Heck Cyclization of Aryl Halides to Afford Indolines
by: Qin, Xurong, et al.
Published: (2018)