Silver catalyzed multicomponent synthesis of aminoindolizines
A direct and efficient approach to 1-aminoindolizines through three component one pot reaction of heteroaryl aldehydes, second amines, and alkynes catalyzed by AgBF4 has been developed. This methodology provides rapid access to construct a diversified oriented library of indolizines.
Saved in:
Main Author: | Bai, Yaguang |
---|---|
Other Authors: | Liu Xuewei |
Format: | Final Year Project |
Language: | English |
Published: |
2010
|
Subjects: | |
Online Access: | http://hdl.handle.net/10356/20852 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Institution: | Nanyang Technological University |
Language: | English |
Similar Items
-
Mn(III)-catalyzed synthesis of pyrroles from vinyl azides and B-keto acids.
by: Ng, Eileen Pei Jian.
Published: (2010) -
Fe(III)- and Au(I)-catalyzed cyclization of arene-alkynes.
by: Gao, Zhi Ming.
Published: (2010) -
Iron-catalyzed directed C2-alkylation and alkenylation of indole with vinylarenes and alkynes
by: Yamakawa, Takeshi, et al.
Published: (2015) -
N-heterocyclic carbene-catalyzed intramolecular stetter reaction between an aldehyde and activated alkyne for easy access to chromones.
by: Wong, Qian Ling.
Published: (2010) -
Yb(OTf)3-catalyzed allenation/ cycloisomerization reaction with propargylic alcohols and amides : a facile synthetic approach to oxazole and its derivatives.
by: Teo, Wan Teng.
Published: (2010)