Results 31 to 40 of about 27,991 (255)

Synthesis of 3-Substituted Pyrrolidines via Palladium-Catalysed Hydroarylation [PDF]

open access: yes, 2018
Metal-catalysed reactions have revolutionised synthetic chemistry, allowing access to unprecedented molecular architectures with powerful properties and activities. Nonetheless, some transformations remain sparse in number, or out of reach, even with the
Joe, Sweeney   +2 more
core   +2 more sources

1,3-Dipolar Cycloadditions of N-Benzyl Furfuryl Nitrones with Electron-rich Alkenes

open access: yesMolecules, 2000
The 1,3-dipolar cycloaddition reaction of N-benzyl-C-(2-furyl)nitrones with electron-rich alkenes gives preferentially trans-substituted 3,5-disubstituted isoxazolidines (endo approach).
Tomas Tejero   +3 more
doaj   +1 more source

Synthesis of 1-phenyl-3-pyrroline in water

open access: yesOrbital: The Electronic Journal of Chemistry, 2012
Pyrrolines are bioactive compounds and can be used as starting materials or as intermediates in the synthesis of natural products [1,2]. N-phenyl-pyrrolines have been prepared by reaction of N-propargylanilines catalyzed by Cu(I) [3] or the ring-closing ...
Thiago Muniz de Souza   +2 more
doaj   +1 more source

Pyrrolidine-2,5-dione [PDF]

open access: yesActa Crystallographica Section E Structure Reports Online, 2012
In the title compound, C(4)H(5)NO(2), the non-H atoms are nearly coplanar, with a maximum deviation of 0.030 (1) Å. In the crystal, pairs of mol-ecules are linked by N-H⋯O hydrogen bonds into inversion dimers.
Min Yu, Xing Huang, Feng Gao
openaire   +3 more sources

Copper(I)-catalyzed asymmetric 1,3-dipolar cycloaddition of 1,3-enynes and azomethine ylides

open access: yesNature Communications, 2023
Herein, we report a copper(I)-catalyzed asymmetric 1,3-dipolar cycloaddition of azomethine ylides and 1,3-enynes, which provides a series of chiral poly-substituted pyrrolidines in high regio-, diastereo-, and enantioselectivities. Both 4-aryl-1,3-enynes
Bo-Ran Wang   +6 more
doaj   +1 more source

Ring Expansion of Vinylaziridines through the Strain-Release Pericyclic Reaction: Recent Developments and Applications

open access: yesMolecules, 2013
Recent syntheses of azetidines, pyrrolidines, piperidines and azepines through cycloaddition or sigmatropic rearrangements of vinylaziridines are described. Applications to natural product synthesis and mechanistic investigations are also summarized.
Yu Mi Heo, Seung-Mann Paek
doaj   +1 more source

Bis(oxotremorine) fumarate bis(fumaric acid)

open access: yesIUCrData, 2022
The title compound, bis(oxotremorine) fumarate bis(fumaric acid) {systematic name: 1-[4-(2-oxopyrrolidin-1-yl)but-2-ynyl]pyrrolidinium (2E)-but-2-enedioate bis[(2E)-but-2-enedioic acid]}, 2C12H19N2O+·C4H2O42−·2C4H4O4, has a single oxotremorine monocation
Marilyn Naeem   +3 more
doaj   +1 more source

Selective Electrochemical Oxidation of Functionalized Pyrrolidines

open access: yes, 2021
A method for the selective electrochemical aminoxyl-mediated Shono-type oxidation of pyrrolidines to pyrrolidinones is described. These transformations show the high selectivity and functional group compatibility. This chemistry also demonstrates the use
Shaoguang Zhang (1652278)   +13 more
core   +1 more source

Reactions affording novel pyrrolidines catalysed by palladium [PDF]

open access: yes
Pyrrolidines are privileged motifs in drug discovery, ranked among the top five most common non-aromatic N-heterocycles and featured in 37 FDA-approved drugs.
Robinson, Joshua, Doulcet, Julien
core   +3 more sources

Construction of N-Aryl-Substituted Pyrrolidines by Successive Reductive Amination of Diketones via Transfer Hydrogenation

open access: yesMolecules
N-aryl-substituted pyrrolidines are important moieties widely found in bioactive substances and drugs. Herein, we present a practical reductive amination of diketones with anilines for the synthesis of N-aryl-substituted pyrrolidines in good to excellent
Jianhua Liao   +4 more
doaj   +1 more source

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