Results 31 to 40 of about 36,836 (288)

Synthesis of Chromen[4,3-b]pyrrolidines by Intramolecular 1,3-Dipolar Cycloadditions of Azomethine Ylides: An Experimental and Computational Assessment of the Origin of Stereocontrol [PDF]

open access: yes, 2015
Azomethine ylides, generated from imine-derived O-cinnamyl or O-crotonyl salicylaldeyde and α-amino acids, undergo intramolecular 1,3-dipolar cycloaddition, leading to chromene[4,3-b]pyrrolidines.
Arrieta, Ana   +8 more
core   +2 more sources

Tetraethyl(pyrrolidine-2,2-diyl)bisphosphonate [PDF]

open access: yesMolecules, 2001
The synthesis of the title compound is already described [1, 2] and we report here the fully optimized procedure.[...]
Olive, Gilles, Jacques, Alain
openaire   +3 more sources

Synthesis of 3-Substituted Pyrrolidines via Palladium-Catalyzed Hydroarylation

open access: yesiScience, 2018
Summary: Metal-catalyzed reactions have revolutionized 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
Joseph B. Sweeney   +2 more
doaj   +1 more source

Regio- and Stereoselective Aminopentadienylation of Carbonyl Compounds [PDF]

open access: yes, 2014
A simple and robust protocol is detailed for the preparation of enantioenriched α-substituted (1,4-pentadien-3-yl)amine derivatives. The methodology involves the addition of an in situ formed pentadienyl indium reagent to chiral tert-butylsulfinimines ...
Bagdatli, Emine   +3 more
core   +2 more sources

6b-Hydroxy-17-methyl-15-(3-nitrophenyl)-6b,7,16,17-tetrahydro-7,14a-methanonaphtho[1′,8′:1,2,3]pyrrolo[3′,2′:8,8a]azuleno[5,6-b]quinolin-14(15H)-one dichloromethane hemisolvate

open access: yesIUCrData, 2016
In the title compound, C34H25N3O4·0.5CH2Cl2, which crystallized as a dichloromethane hemisolvate, the central 1-methylpyrrolidine ring adopts an envelope conformation with the N atom as the flap.
J. M. Joseph   +2 more
doaj   +1 more source

Site-Selective Modification of a Porpholactone—Selective Synthesis of 12,13- and 17,18-Dihydroporpholactones

open access: yesMolecules, 2020
The reaction of meso-tetrakis(pentafluorophenyl)porpholactone with azomethine ylides and nitrones affords pyrrolidine-fused and isoxazolidine-fused dihydroporpholactones that display, respectively, isobacteriochlorin- and chlorin-type UV–Vis spectra ...
Ana F. R. Cerqueira   +5 more
doaj   +1 more source

Buflomedil for intermittent claudication [PDF]

open access: yes, 2013
Background : Intermittent claudication (IC) is pain caused by chronic occlusive arterial disease, that develops in a limb during exercise and is relieved with rest. Buflomedil is a vasoactive agent used to treat peripheral vascular disease.
De Backer, Tine, Vander Stichele, Robert
core   +2 more sources

Synthesis of dienes from pyrrolidines using skeletal modification

open access: yesNature Communications, 2023
Saturated N-heterocyclic pyrrolidines are common in natural products, medicinal compounds and agrochemicals. However, reconstruction of their skeletal structures creating new chemical space is a challenging task, and limited methods exist for this ...
Haitao Qin   +4 more
doaj   +1 more source

Effect of Some Synthesized Pyrrolidines in Growth of L. infantum Promastigotes

open access: yesTikrit Journal of Pure Science, 2023
In this research, three pyrrolidine compounds (P1-P3) were synthesized and then tested for efficacy against L. infantum promastigotes in vitro. The study included preparation of some chalcones and schiff bases then the condensation of both to get the
Haitham L. Al-Hayali   +2 more
doaj   +1 more source

A New Class of Substrates for Nucleophilic 5-endo-trig Cyclization, 2-Trifluoromethyl-1-alkenes: Synthesis of Five-Membered Hetero- and Carbocycles That Bear Fluorinated One-Carbon Units [PDF]

open access: yes, 2008
Disfavored 5-endo-trig cyclizations were achieved in 2-trifluoromethyl-1-alkenes with a nucleophilic nitrogen, oxygen, sulfur, or carbon atom through 1) intramolecular SN2 reaction with loss of a fluoride ion or 2) intramolecular nucleophilic addition to
Ichikawa Junji   +5 more
core   +1 more source

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