Results 91 to 100 of about 11,995 (215)

Organocatalytic asymmetric domino Michael/O-alkylation reaction for the construction of succinimide substituted 3(2H)-furanones catalyzed by quinine

open access: yes, 2017
Asymmetric domino reaction of maleimides with γ-halogenated-β-ketoesters catalyzed by quinine is developed to give succinimide substituted 3(2H)-furanones in good enantioselectivities.
Zongjie Gan   +7 more
core   +1 more source

Time-Economical Radical Cascade Cyclization/Haloazidation of 1,6-Enynes: Construction of Highly Functional Succinimide Derivatives

open access: yes, 2020
A “time-economical” radical cascade cyclization/haloazidation of 1,6-enynes provides a direct approach to access highly functional succinimide compounds.
Liming Zhao (2329306)   +6 more
core   +1 more source

(3R,3aS,6aR)-2,5-Dimethyl-3-(5-phenyl-2-thienyl)perhydropyrrolo[3,4-d][1,2]oxazole-4,6-dione

open access: yesActa Crystallographica Section E, 2008
The crystal structure of the title compound, C17H16N2O3S, exhibits intramolecular C—H...S and intermolecular C—H...S and C—H...O hydrogen bonds, C—S...N [S...N = 3.033 (2) Å and C—S...N = 142.76 (9 ...
Mustafa Odabaşoğlu   +3 more
doaj   +1 more source

1-(Anthracen-1-yl)pyrrolidine-2,5-dione

open access: yesActa Crystallographica Section E, 2012
In the molecular structure of title compound, C18H13NO2, the succinimide ring is orientated away from the plane of the anthracene moiety by 71.94 (4)°. The crystal structure features three different types of intermolecular interactions,
Sanaz Khorasani, Manuel A. Fernandes
doaj   +1 more source

Succinimide thioether in peptid ligation - method developement and structure elucidation

open access: yes, 2018
Die regioselektive Reaktion von Maleimiden mit einem Thiol unter Ausbildung eines Succinimid Thioethers ist eine weit verbreitete Methode zur Konjugation von Biomolekülen oder zur Funktionalisierung von Oberflächen.
Lenz, Stefan
core   +1 more source

pH Dependence of Succinimide-Ester-Based Protein Cross-Linking for Structural Mass Spectrometry Applications

open access: yes, 2021
Within the research field of cross-linking mass spectrometry (XL-MS), the most commonly used cross-linking reagents are succinimide-ester-based (e.g., disuccinimidyl suberate (DSS)). These reagents primarily cross-link lysine side chains.
Esben Trabjerg (1540687)   +5 more
core   +1 more source

Dual reactivity of imidic carbonyl ylides in Rh(II)-catalyzed reactions of alpha-diazocarbonyl compounds with succinimide [PDF]

open access: yes, 2006
Stabilization of imidic carbonyl ylides derived from alpha-diazocarbonyl compounds and succinimide occurs in two different ways: ylides from diazoesters experience a [1,4]-hydrogen shift to produce the corresponding O-alkylimidates while their analogues ...
Heimgartner, Heinz   +4 more
core   +1 more source

Design of pyrrolidine-2, 5-dione Schiff’s base derivatives as GABAA inhibitors for antiepileptic activity

open access: yesMediterranean Journal of Pharmacy and Pharmaceutical Sciences
Succinimide derivatives are an essential class of compounds with diverse pharmacological applications. Different derivatives of succinimide as Schiff’s base were designed for good inhibitory activity against the human GABAA receptor.
Omran N.R. Fhaid
doaj   +1 more source

On-Demand Thio-Succinimide Hydrolysis for the Assembly of Stable Protein-Protein Conjugates. [PDF]

open access: yes
Chemical post-translational protein-protein conjugation is an important technique with growing applications in biotechnology and pharmaceutical research. Maleimides represent one of the most widely employed bioconjugation reagents.

core   +4 more sources

STUDIES IN ORGANO-ARSENIC COMPOUNDS. PART IX. SYNTHESIS OF ARSENIC ANALOGUE OF SUCCINIMIDE

open access: yes, 1938
Arsenic analogue of succinimide has been synthesised by the application of Fittig's reaction to a mixture of succinyl chloride and pheuyldichloroarsine in xylene solution. The constitution of the succinylphenylarsine has been established by its reduction
HIRENDRA NATH DAS-GUPTA
core   +1 more source

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