phosphine has been researched along with cyclopentane 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 | 5 (45.45) | 29.6817 |
2010's | 6 (54.55) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Krische, MJ; Wang, JC | 1 |
Koech, PK; Krische, MJ | 1 |
Fu, GC; Wilson, JE | 1 |
Lu, X; Lu, Z; Zhang, X; Zheng, S | 1 |
Guan, XY; Shi, M | 1 |
Barbas, CF; Candeias, NR; Tan, B | 1 |
Chen, R; Geng, Z; Hu, C; Huang, Y; Ma, J | 1 |
Carry, JC; Gicquel, M; Gomez, C; Marinetti, A; Retailleau, P; Schio, L; Voituriez, A | 1 |
Chen, XQ; Huang, YZ; Kantchev, EA; Qin, HL | 1 |
Bower, JF; Croft, RA; Shaw, MH; Whittingham, WG | 1 |
Chen, W; Gao, X; Guo, H; Li, Z; Liu, Y; Yang, W; Zhang, C; Zheng, L | 1 |
11 other study(ies) available for phosphine and cyclopentane
Article | Year |
---|---|
Intramolecular organocatalytic [3+2] dipolar cycloaddition: stereospecific cycloaddition and the total synthesis of (+/-)-hirsutene.
Topics: Catalysis; Cyclopentanes; Molecular Structure; Phosphines; Polycyclic Sesquiterpenes; Sesquiterpenes; Stereoisomerism | 2003 |
Phosphine catalyzed alpha-arylation of enones and enals using hypervalent bismuth reagents: regiospecific enolate arylation via nucleophilic catalysis.
Topics: Aldehydes; Bismuth; Catalysis; Cyclohexanones; Cyclopentanes; Indicators and Reagents; Molecular Structure; Phosphines | 2004 |
Synthesis of functionalized cyclopentenes through catalytic asymmetric [3+2] cycloadditions of allenes with enones.
Topics: Alkenes; Catalysis; Cyclization; Cyclopentanes; Ketones; Molecular Structure; Phosphines; Stereoisomerism | 2006 |
An unexpected phosphine-catalyzed [3 + 2] annulation. Synthesis of highly functionalized cyclopentenes.
Topics: Alkadienes; Catalysis; Cyclization; Cyclopentanes; Nitriles; Phosphines | 2008 |
Phosphine-mediated [3+2] cycloaddition reactions of ethyl 5,5-diarylpenta-2,3,4-trienoates with arylmethylidenemalononitriles and N-tosylimines.
Topics: Cyclization; Cyclopentanes; Imines; Molecular Structure; Nitriles; Phosphines; Pyrrolidines; Stereoisomerism; Tosyl Compounds | 2009 |
Core-structure-motivated design of a phosphine-catalyzed [3+2] cycloaddition reaction: enantioselective syntheses of spirocyclopenteneoxindoles.
Topics: Catalysis; Cyclization; Cyclopentanes; Indoles; Molecular Structure; Phosphines; Spiro Compounds; Stereoisomerism | 2011 |
Phosphine-catalyzed Rauhut-Currier domino reaction: a facile strategy for the construction of highly functionalized cyclopentene.
Topics: Carbon; Catalysis; Cycloaddition Reaction; Cyclopentanes; Phosphines | 2012 |
Phosphine-catalyzed synthesis of 3,3-spirocyclopenteneoxindoles from γ-substituted allenoates: systematic studies and targeted applications.
Topics: Alkadienes; Catalysis; Cyclization; Cyclopentanes; Indoles; Molecular Structure; Phosphines; Spiro Compounds | 2013 |
A first-principles examination of the asymmetric induction model in the binap/Rh(I)-catalysed 1,4-addition of phenylboronic acid to cyclic enones by density functional theory calculations.
Topics: Boronic Acids; Catalysis; Cyclization; Cyclohexanones; Cyclopentanes; Ketones; Models, Molecular; Phosphines; Rhodium; Stereoisomerism | 2014 |
Modular Access to Substituted Azocanes via a Rhodium-Catalyzed Cycloaddition-Fragmentation Strategy.
Topics: Alkenes; Catalysis; Cycloaddition Reaction; Cyclopentanes; Heterocyclic Compounds, 1-Ring; Phosphines; Rhodium | 2015 |
Phosphine-catalyzed [3 + 2] and [4 + 2] annulation reactions of ynones with barbiturate-derived alkenes.
Topics: Alkenes; Barbiturates; Catalysis; Cyclopentanes; Ketones; Molecular Structure; Phosphines; Spiro Compounds | 2017 |