2-oxindole has been researched along with 4-butyrolactone in 7 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 0 (0.00) | 29.6817 |
2010's | 7 (100.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Jia, X; Li, C; Li, J; Liu, Y | 1 |
Bergonzini, G; Melchiorre, P | 1 |
Chen, YC; Dong, L; Huang, X; Peng, J | 1 |
Dong, WP; Shi, XM; Wang, L; Wang, R; Zhu, LP | 1 |
Murata, Y; Sakamoto, M; Sengoku, T; Takahashi, M; Yagishita, F; Yoda, H | 2 |
Li, T; Tu, S; Xie, Y; Yao, C; Yu, C | 1 |
7 other study(ies) available for 2-oxindole and 4-butyrolactone
Article | Year |
---|---|
Syntheses of spirocyclic oxindole-butenolides by using three-component cycloadditions of isocyanides, allenoates, and isatins.
Topics: 4-Butyrolactone; Cyanides; Cyclization; Indoles; Isatin; Molecular Structure; Naphthalenes; Oxindoles; Spiro Compounds; Stereoisomerism | 2011 |
Dioxindole in asymmetric catalytic synthesis: routes to enantioenriched 3-substituted 3-hydroxyoxindoles and the preparation of maremycin A.
Topics: 4-Butyrolactone; Aldehydes; Catalysis; Indoles; Oxindoles; Spiro Compounds; Stereoisomerism | 2012 |
Asymmetric assembly of 2-oxindole and α-angelica lactone units to construct vicinal quaternary chiral centers.
Topics: 4-Butyrolactone; Amines; Catalysis; Indoles; Lewis Bases; Oxindoles; Stereoisomerism | 2012 |
Efficient construction of highly functionalized spiro[γ-butyrolactone-pyrrolidin-3,3'-oxindole] tricyclic skeletons via an organocatalytic 1,3-dipolar cycloaddition.
Topics: 4-Butyrolactone; Catalysis; Cycloaddition Reaction; Esters; Indoles; Oxindoles; Pyrrolidines; Spiro Compounds | 2013 |
Construction of spiro-fused 2-oxindole/α-methylene- γ-butyrolactone systems with extremely high enantioselectivity via indium-catalyzed amide allylation of N-methyl isatin.
Topics: 4-Butyrolactone; Amides; Catalysis; Indium; Indoles; Isatin; Molecular Structure; Organometallic Compounds; Oxindoles; Spiro Compounds; Stereoisomerism | 2013 |
Catalytic enantioselective amide allylation of isatins and its application in the synthesis of 2-oxindole derivatives spiro-fused to the α-methylene-γ-butyrolactone functionality.
Topics: 4-Butyrolactone; Amides; Catalysis; Indoles; Isatin; Models, Molecular; Molecular Structure; Oxindoles; Spiro Compounds; Stereoisomerism | 2014 |
An NHC-catalyzed in situ activation strategy to β-functionalize saturated carboxylic acid: an enantioselective formal [3+2] annulation for spirocyclic oxindolo-γ-butyrolactones.
Topics: 4-Butyrolactone; Carbolines; Carboxylic Acids; Catalysis; Indoles; Oxindoles; Spiro Compounds; Stereoisomerism | 2015 |