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2‐Nitrobenzyl Isocyanide as a Universal Convertible Isocyanide [PDF]

open access: yesAsian Journal of Organic Chemistry, 2017
Abstract2‐Nitrobenzyl isocyanide is reported as a universal convertible isocyanide with extensive applicability in both Ugi four‐component reaction (Ugi‐4CR) and Ugi‐tetrazole reaction. The cleavage of this isocyanide from 17 examples in both acidic and basic conditions is presented.
Ajay L Chandgude   +2 more
exaly   +6 more sources

Efficient Isocyanide-less Isocyanide-Based Multicomponent Reactions [PDF]

open access: yesOrganic Letters, 2015
Isocyanides are the "Jekyll and Hyde" of organic chemistry allowing for extremely interesting transformations that are not only extremely odorous but also noxious. Therefore, an isocyanide-less isocyanide-based multicomponent reaction (IMCR) has been developed, and this protocol is expected to replace many of the old procedures in the future not only ...
Neochoritis   +4 more
openaire   +5 more sources

The isocyanide SN2 reaction [PDF]

open access: yesNature Communications, 2023
Abstract The S N 2 nucleophilic substitution reaction is a vital organic transformation used for drug and natural product synthesis. Nucleophiles like cyanide, oxygen, nitrogen, sulfur, or phosphorous replace halogens or sulfonyl esters, forming new bonds.
Pravin Patil   +3 more
openaire   +5 more sources

Synthesis and structure of a tetrahedral homoleptic CuI complex with xylyl isocyanide [PDF]

open access: yesActa Crystallographica Section E: Crystallographic Communications
Treatment of the CuI precursor [Cu(NCMe)4]PF6 with excess (10 equivalents) of relatively bulky xylyl isocyanide formed a tetra(isocyanide) complex, namely, tetrakis(2,6-dimethylphenylisocyanide)copper(I) hexafluorophosphate, [Cu(C9H9N)4]PF6 or [Cu(CNXyl ...
A. M. Buddhika Chandima   +2 more
doaj   +2 more sources

Investigating the bioorthogonality of isocyanides.

open access: yesChem Commun (Camb)
Isocyanides have been explored as bioorthogonal triggers for uncaging reactions. However, our findings show they can covalently label proteins, indicating they may not be fully bioorthogonal in biological systems.
Nakao R   +7 more
europepmc   +5 more sources

Isocyanide 2.0 [PDF]

open access: yesGreen Chemistry, 2020
Isocyanides are important chemicals, with limited availability, thus reducing their general use. Our highly improved isocyanide synthesis performed on mole to μ-mole scale, individually or in a 96-well parallel fashion enables unprecedented exploration of novel chemistries.
Pravin Patil   +2 more
openaire   +4 more sources

(tert-Butyl isocyanide-κC)trichloridogallium(III)

open access: yesIUCrData, 2016
The crystal structure of (tert-butyl isocyanide-κC)trichloridogallium(III), [GaCl3(C5H9N)], features the first reported isocyanide–gallium trihalide complex. The Ga—C—N—C fragment is essentially linear.
Jeremy L. Bourque   +2 more
doaj   +2 more sources

Tris(tert-butyl isocyanide-κC)carbonylnickel(0)

open access: yesActa Crystallographica Section E, 2008
The title compound, [Ni(C5H9N)3(CO)], was prepared from Ni(CO)4 and a tenfold excess of tert-butyl isocyanide. It crystallizes with two symmetry-independent molecules per asymmetric unit.
Wolfgang Imhof   +2 more
doaj   +2 more sources

Urea Synthesis from Isocyanides and O-Benzoyl Hydroxylamines Catalyzed by a Copper Salt

open access: yesMolecules, 2022
In the presence of CuOAc, a series of unsymmetric ureas can be generated in moderate to good yields under mild reaction conditions (10 mol% of CuOAc, 2 equiv t-BuONa or PhONa, 30 °C), using aryl isocyanides and O-benzoyl hydroxylamines as the readily ...
Ning Yu   +5 more
doaj   +1 more source

Medicinal Chemistry of Isocyanides [PDF]

open access: yesChemical Reviews, 2021
In eons of evolution, isocyanides carved out a niche in the ecological systems probably thanks to their metal coordinating properties. In 1859 the first isocyanide was synthesized by humans and in 1950 the first natural isocyanide was discovered. Now, at the beginning of XXI century, hundreds of isocyanides have been isolated both in prokaryotes and ...
Alberto Massarotti   +4 more
openaire   +4 more sources

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