Results 91 to 100 of about 17,027 (206)

Regioselective Synthesis of 3-Substituted Pyrroles by Nucleophilic Addition of 3-(1-Arylsulfonylalkyl) Pyrroles Activated under Basic or Acid Conditions [PDF]

open access: yes, 2011
Sulfonyl pyrroles, obtained regioselectively from commercial N-triisopropylsilylpyrrole, undergo removal of the arylsulfonyl group under basic or acidic conditions to give vinylogous imino-like derivatives (see scheme; TIPS=triisopropylsilyl).
MARTINELLI, FABIO   +5 more
core   +1 more source

Facile Synthesis of N-Aryl Pyrroles via Cu(II)-Mediated Cross Coupling of Electron Deficient Pyrroles and Arylboronic Acids [PDF]

open access: yes, 2016
N-Arylation of electron-deficient pyrroles has been achieved by cross-coupling with arylboronic acids at room temperature in the presence of stoichiometric amounts of copper(II) acetate. The generality of this reaction has been established with variously
Jayaram K. Srirangam (2998734)   +2 more
core   +1 more source

N-Heterocyclic carbene–palladium catalysts for the direct arylation of pyrrole derivatives with aryl chlorides

open access: yesBeilstein Journal of Organic Chemistry, 2013
New Pd–NHC complexes have been synthesized and employed for palladium-catalyzed direct arylation of pyrrole derivatives by using electron-deficient aryl chlorides as coupling partners.
Ismail Özdemir   +6 more
doaj   +1 more source

Synthesis and in vitro study of redox properties of pyrrole and halogenated pyrrole derivatives [PDF]

open access: yesJournal of the Serbian Chemical Society
The redox balance plays a crucial role in maintaining biological processes under normal conditions. Antioxidants inhibit and reduce harmful oxidation processes, while pro-oxidants can act as anti-cancer agents by promoting ROS-mediated cell death.
Petković Miloš R.   +7 more
doaj   +1 more source

Application of Flow Thermolysis in Organic Synthesis: Easy Access to α,ω-Bis Thienyl- and Bis Pyrrolyl- Alkanes from Methylene Derivatives of Meldrum's Acid

open access: yesMolecules, 2000
Thermal decomposition of Meldrum's acid derivatives and rearrangement of (alkylsulfanyl) or (propargylamino)methylene ketene intermediates leads in one step to bis thienyl- or bis pyrrolyl-alkanes.
Hamid Dhimane   +2 more
doaj   +1 more source

Rhodium-Catalyzed Transannulation of 1,2,3-Triazoles to Polysubstituted Pyrroles [PDF]

open access: yes, 2016
Rhodium-catalyzed transannulation of N-sulfonyl-1,2,3-triazoles with vinyl ether has been accomplished for the synthesis of various polysubstituted pyrroles.
Pazhamalai Anbarasan (1555108)   +1 more
core   +1 more source

Synthesis of N-(o-amino aryl) pyrroles by Paal-Knorr reaction [PDF]

open access: yes, 1971
N-(o-nitro aryl)- and N-(o-acetamino aryl)-2, 5-dimethyl pyrroles are synthesized by Paal-Knorr reaction by condensing acetonyl acetone with o-nitro anilines and o-acetamino anilines respectively.
Subba Rao, N. V.   +2 more
core   +1 more source

Controlled oxidation of pyrroles: synthesis of highly functionalized γ-lactams [PDF]

open access: yes, 2013
The oxidation of pyrroles usually leads to uncontrolled polymerization and decomposition. To overcome this problem, the controlled oxidation of substituted pyrroles with Dess-Martin periodinane is reported.
Jason Smith (14749684)   +3 more
core  

Substituent effect on the electronic and optical properties of newly designed pyrrole derivatives using density functional theory

open access: yesOpen Physics
This work explores six newly designed compounds obtained by several substitutions in 2,5-di(2-thienyl) pyrrole molecule. For this series of compounds, the electronic and optical properties were investigated using density functional theory and time ...
Aljaafreh Mamduh J., Hussein Rageh. K.
doaj   +1 more source

Nouvelle synthèse de pyrroles par cycloaddition [3+2] intramoléculaire [PDF]

open access: yes, 2004
La cycloaddition dipolaire-1,3 est devenue un outil synthétique puissant permettant la synthèse d'hétérocycles azotés à cinq chaînons. Dans ce travail nous avons mis au point une nouvelle synthèse de pyrroles par cycloaddition.
BASHIARDES, Georges   +2 more
core  

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