2018
DOI: 10.1039/c8ob01005f
|View full text |Cite
|
Sign up to set email alerts
|

Palladium-catalyzed selective synthesis of 3,4-dihydroquinazolines from electron-rich arylamines, electron-poor arylamines and glyoxalates

Abstract: A simple palladium-catalyzed selective synthesis of structurally diverse 3,4-dihydroquinazolines from electron-rich arylamines, electron-poor arylamines and glyoxalates has been developed under mild conditions. This reaction is carried out in a tandem manner constituted by the condensation of arylamines and glyoxalates, the selective Diels-Alder cycloaddition and oxidation processes, in which 4-nitrothiophenol was used as the key ligand.

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
5

Citation Types

0
9
0

Year Published

2018
2018
2020
2020

Publication Types

Select...
10

Relationship

6
4

Authors

Journals

citations
Cited by 47 publications
(9 citation statements)
references
References 58 publications
0
9
0
Order By: Relevance
“…As part of our ongoing research interest in the green synthesis, we have reported the eco-friendly functionalization of alkynes. In this paper, we report for the first time an economical and eco-friendly protocol for the synthesis of various Z -vinyl selenolates through natural DES (ChCl/glycolic acid) catalyzed selenocyanation of activated alkynes (Scheme c).…”
Section: Introductionmentioning
confidence: 99%
“…As part of our ongoing research interest in the green synthesis, we have reported the eco-friendly functionalization of alkynes. In this paper, we report for the first time an economical and eco-friendly protocol for the synthesis of various Z -vinyl selenolates through natural DES (ChCl/glycolic acid) catalyzed selenocyanation of activated alkynes (Scheme c).…”
Section: Introductionmentioning
confidence: 99%
“…However, to the best of our knowledge, the preparation of quinolin-2-yl substituted ureas from readily available quinoline N -oxides has never been reported. In continuation of our research program in green and sustainable chemistry, we have reported the ecofriendly preparation of N -heterocycles and their derivatives. In this paper, we report an environmentally friendly method for the clean preparation of quinolin-2-yl substituted ureas from readily available quinoline N -oxides and carbodiimides in water (Scheme d).…”
Section: Introductionmentioning
confidence: 99%
“…In continuation of our studies in sustainable chemistry, herein we report a clean and practical strategy for the preparation of a variety of Z-β-thiocyanate alkenyl esters. The ecofriendly lactic acid plays a dual function in the quantitative transformation, serving as a recyclable catalyst and reaction medium.…”
Section: Introductionmentioning
confidence: 99%