2021
DOI: 10.1016/j.jorganchem.2021.122073
|View full text |Cite
|
Sign up to set email alerts
|

Recyclable heterogeneous iron supported on imidazolium ionic liquid catalysed palladium and copper-free Heck reaction

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2

Citation Types

0
2
0

Year Published

2022
2022
2024
2024

Publication Types

Select...
5

Relationship

0
5

Authors

Journals

citations
Cited by 6 publications
(2 citation statements)
references
References 34 publications
0
2
0
Order By: Relevance
“…In 2021, the group led by Parasuraman developed a green, non‐toxic chloroglycine ‐ ionic liquid imidazolium supported Fe(III) complex, [Gmim]Cl−Fe(III)] for Mizoroki‐Heck coupling of olefins [68] . Among several bases screened, NEt 3 (2 mmol) proved to be efficient for the Heck reaction between aromatic halides 34 and styrene 28 under solvent free conditions at 80 °C (Scheme 40).…”
Section: Iron‐catalyzed Reactionsmentioning
confidence: 99%
See 1 more Smart Citation
“…In 2021, the group led by Parasuraman developed a green, non‐toxic chloroglycine ‐ ionic liquid imidazolium supported Fe(III) complex, [Gmim]Cl−Fe(III)] for Mizoroki‐Heck coupling of olefins [68] . Among several bases screened, NEt 3 (2 mmol) proved to be efficient for the Heck reaction between aromatic halides 34 and styrene 28 under solvent free conditions at 80 °C (Scheme 40).…”
Section: Iron‐catalyzed Reactionsmentioning
confidence: 99%
“…In 2021, the group led by Parasuraman developed a green, non-toxic chloroglycine -ionic liquid imidazolium supported Fe(III) complex, [Gmim]ClÀ Fe(III)] for Mizoroki-Heck coupling of olefins . [68] Among several bases screened, NEt 3 (2 mmol) proved to be efficient for the Heck reaction between aromatic halides 34 and styrene 28 under solvent free conditions at 80 °C (Scheme 40). Substrate scope studies indicated that functionalized aromatic halides containing both electron-donating and electron-withdrawing groups efficiently coupled with styrene to give the corresponding products 29 in 73-95 % yields with complete trans-selectivity.…”
Section: Iron-catalyzed Reactionsmentioning
confidence: 99%