pyrroles has been researched along with folicanthine in 11 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 2 (18.18) | 29.6817 |
| 2010's | 9 (81.82) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Movassaghi, M; Schmidt, MA | 1 |
| Gao, JM; Jarussophon, S; Konishi, Y; Ma, YT; Xu, T; Zhang, JW; Zhang, XC | 1 |
| Chen, PH; Gong, LZ; Guo, C; Huang, JZ; Luo, SW; Song, J | 1 |
| Ali, S; Li, YX; Liang, YM; Wang, HX; Xia, XF | 1 |
| Kanai, M; Matsunaga, S; Mitsunuma, H; Shibasaki, M | 1 |
| Luo, L; Peng, Y; Wang, YW; Yan, CS; Zhang, JJ | 1 |
| Murata, T; Oguri, H; Oikawa, H; Wada, M | 1 |
| Bisai, A; Chaudhuri, S; Ghosh, S | 2 |
| Ding, M; Liang, K; Pan, R; Xia, C; Zhang, H | 1 |
| Babu, KN; Bisai, A; Kinthada, LK; Medisetty, SR; Parida, A | 1 |
11 other study(ies) available for pyrroles and folicanthine
| Article | Year |
|---|---|
Concise total synthesis of (-)-calycanthine, (+)-chimonanthine, and (+)-folicanthine.
Topics: Indoles; Molecular Conformation; Naphthyridines; Pyrroles; Stereoisomerism | 2007 |
Antifungal activity of alkaloids from the seeds of Chimonanthus praecox.
Topics: Antifungal Agents; Calycanthaceae; Fungi; Indoles; Microbial Sensitivity Tests; Naphthyridines; Pyrroles; Seeds | 2009 |
Core-structure-oriented asymmetric organocatalytic substitution of 3-hydroxyoxindoles: application in the enantioselective total synthesis of (+)-folicanthine.
Topics: Carbamates; Catalysis; Indoles; Oxindoles; Phosphoric Acids; Pyrroles; Stereoisomerism | 2012 |
Iodine-mediated regioselective C2-amination of indoles and a concise total synthesis of (±)-folicanthine.
Topics: Amination; Cyclization; Dimerization; Indoles; Iodine; Pyrroles; Stereoisomerism | 2012 |
Catalytic asymmetric total synthesis of chimonanthine, folicanthine, and calycanthine through double Michael reaction of bisoxindole.
Topics: Catalysis; Indoles; Naphthyridines; Pyrroles; Stereoisomerism | 2012 |
Ni-catalyzed reductive homocoupling of unactivated alkyl bromides at room temperature and its synthetic application.
Topics: Bromides; Catalysis; Dimerization; Furans; Hydrocarbons, Brominated; Indoles; Molecular Structure; Nickel; Pyrroles; Stereoisomerism; Temperature | 2013 |
Nickel-catalyzed dimerization of pyrrolidinoindoline scaffolds: systematic access to chimonanthines, folicanthines and (+)-WIN 64821.
Topics: Catalysis; Dimerization; Indoles; Molecular Structure; Nickel; Piperazines; Pyrroles; Stereoisomerism | 2014 |
Oxidative dimerization of 2-oxindoles promoted by KO(t)Bu-I₂: total synthesis of (±)-folicanthine.
Topics: Catalysis; Dimerization; Hydrocarbons, Iodinated; Indole Alkaloids; Indoles; Molecular Structure; Oxidative Coupling; Oxindoles; Pyrroles; Stereoisomerism | 2015 |
Total Synthesis of (+)-Chimonanthine, (+)-Folicanthine, and (-)-Calycanthine.
Topics: Catalysis; Indole Alkaloids; Indoles; Molecular Structure; Naphthyridines; Pyrroles; Stereoisomerism | 2015 |
Catalytic Enantioselective Decarboxylative Allylations of a Mixture of Allyl Carbonates and Allyl Esters: Total Synthesis of (-)- and (+)-Folicanthine.
Topics: Allyl Compounds; Carbonates; Catalysis; Esters; Indoles; Molecular Structure; Naphthyridines; Pyrroles; Stereoisomerism | 2015 |
FeCl
Topics: Allyl Compounds; Catalysis; Chlorides; Ferric Compounds; Indoles; Molecular Structure; Oxindoles; Pyrroles; Stereoisomerism | 2017 |