Results 41 to 50 of about 163,500 (335)

Decarboxylative Cross-Electrophile Coupling of N-Hydroxyphthalimide Esters with Aryl Iodides

open access: yesJournal of the American Chemical Society, 2016
A new method for the decarboxylative coupling of alkyl N-hydroxyphthalimide esters (NHP esters) with aryl iodides is presented. In contrast to previous studies that form alkyl radicals from carboxylic acid derivatives, no photocatalyst, light, or ...
Kierra M. M. Huihui   +9 more
semanticscholar   +1 more source

Aromatic Iodides: Synthesis and Conversion to Heterocycles

open access: yesChemistry Proceedings, 2022
Aromatic heterocycles can be found in many molecules endowed with specific properties, in particular for applications in the fields of medicinal chemistry and materials science.
Florence Mongin   +2 more
doaj   +1 more source

Effect of 2-Substitution on the Rearrangement of 1-Cyclopropylvinyl Cations [PDF]

open access: yes, 1973
2-Substitution in 1-cyclopropylvinyl cations produces a steric effect on cation generation and solvent trapping, but an electronic charge-stabilizing effect on cyclopropyl-to-cyclobutyl ...
Bergman, Robert G., Kelsey, Donald R.
core   +1 more source

Synthesis of chiral cyclohexanes and carbasugars by 6-exo-dig radical cyclisation reactions

open access: yesBeilstein Journal of Organic Chemistry, 2008
Treatment of 5-(tert-butyldimethylsilyl)-2,3-O-isopropylidene-D-ribose with lithium acetylides gave mixtures of syn- and anti-alkynols 2a–2c which were separated following protection as methoxymethyl ethers.
Rajeev K. Shrivastava   +4 more
doaj   +1 more source

Synthesis of substituted Z-styrenes by Hiyama-type coupling of oxasilacycloalkenes: application to the synthesis of a 1-benzoxocane

open access: yesBeilstein Journal of Organic Chemistry, 2017
Several Hiyama cross-coupling reactions of oxasilacycloalkenes and aryl iodides are described that produce trisubstituted Z-styrenes in moderate to excellent yields.
James R. Vyvyan   +5 more
doaj   +1 more source

Palladium-catalyzed difluoromethylation of heteroaryl chlorides, bromides and iodides. [PDF]

open access: yes, 2017
A palladium-catalyzed difluoromethylation of a series of heteroaryl chlorides, bromides and iodides under mild conditions is described. A wide range of heteroaryl halides such as pyridyl, pyrimidyl, pyrazyl, funanyl, thienyl, pyazolyl, imidazolyl ...
Gu, Yang   +4 more
core   +1 more source

Crystal structure and Hirshfeld surface analysis of chiral catena-poly[l-histidinediium [[diiodidocuprate(I)]-μ-iodido] monohydrate]

open access: yesActa Crystallographica Section E: Crystallographic Communications
The title compound, {(C6H11N3O2)[CuI3]·H2O}n or (L-HisH2)CuI3·H2O (1), is a chiral organic–inorganic compound that crystallizes in the monoclinic P21 space group.
Valerii Y. Sirenko   +4 more
doaj   +1 more source

A Simple and Effective Protocol for One-Pot Diazotization-Iodination of Aromatic Amines by Acidic Ionic Liquid [H-NMP]HSO4 at Room Temperature [PDF]

open access: yesIranian Journal of Chemistry & Chemical Engineering, 2011
A simple and efficient one-pot method for the preparation of aromatic iodides has been developed by sequential diazotization–iodination of aromatic amines employing sodium nitrite and sodium iodide in the presence of acidic ionic liquid N-methyl-2 ...
Abdolreza Hajipour   +1 more
doaj  

Synthesis of novel room temperature chiral ionic liquids. application as reaction media for the heck arylation of aza-endocyclic acrylates. [PDF]

open access: yes, 2010
New achiral and chiral RTILs were prepared using novel and/or optimized synthetic routes. These new series of imidazolinium, imidazolium, pyridinium and nicotine-derived ionic liquids were fully characterized including differential scanning calorimetry ...
Correia, Carlos R. D.   +4 more
core   +4 more sources

Palladium(II)/Cationic 2,2’-Bipyridyl System as a Highly Efficient and Reusable Catalyst for the Mizoroki-Heck Reaction in Water

open access: yesMolecules, 2010
A water-soluble and air-stable Pd(NH3)2Cl2/cationic 2,2’-bipyridyl system was found to be a highly-efficient and reusable catalyst for the coupling of aryl iodides and alkenes in neat water using Bu3N as a base.
Fu-Yu Tsai   +2 more
doaj   +1 more source

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