2013
DOI: 10.1016/j.tetlet.2013.08.002
|View full text |Cite
|
Sign up to set email alerts
|

Corrigendum to “The Michael addition of 1,2-cyclohexanedione to β-nitrostyrenes (I): the synthesis of 3-aryl-5,6-dihydrobenzofuran-7(4H)-ones” [Tetrahedron Lett. 54 (2013) 3371–3373]

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1

Citation Types

0
1
0

Year Published

2015
2015
2019
2019

Publication Types

Select...
4

Relationship

0
4

Authors

Journals

citations
Cited by 4 publications
(1 citation statement)
references
References 0 publications
0
1
0
Order By: Relevance
“…Owing to the ability to take part in a wide range of organic reactions and easy accessibility through nitro‐ aldol condensation, nitroalkenes have been used to synthesize a number of heterocycles such as furan,,, imidazole, pyridine, pyrimidine, indole, imidazopyridine,,, etc . Notably, nitroalkene is bielectrophilic in nature and could serve as potential precursor to form heterocycles by reacting with binucleophiles via cascade hetero‐Michael addition reaction .…”
Section: Introductionmentioning
confidence: 99%
“…Owing to the ability to take part in a wide range of organic reactions and easy accessibility through nitro‐ aldol condensation, nitroalkenes have been used to synthesize a number of heterocycles such as furan,,, imidazole, pyridine, pyrimidine, indole, imidazopyridine,,, etc . Notably, nitroalkene is bielectrophilic in nature and could serve as potential precursor to form heterocycles by reacting with binucleophiles via cascade hetero‐Michael addition reaction .…”
Section: Introductionmentioning
confidence: 99%