Results 161 to 170 of about 7,368,504 (211)
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3D printed nanocomposites using polymer grafted graphene oxide prepared by multicomponent Passerini reaction

, 2020
The surface of commercial graphene oxide was modified with polymers using Passerini reaction, which enhances the compatibility between nanoparticles and 3D printing resin.
Guannan Wang   +5 more
semanticscholar   +1 more source

A new modification of the Passerini reaction: a one-pot synthesis of α-acyloxyamides via sequential Kornblum oxidation/Passerini reaction

Tetrahedron Letters, 2015
Abstract A novel approach for the synthesis of α-acyloxyamides is described. Benzylic substrates (halides or tosylates), under mild Kornblum conditions, are oxidized to give the corresponding aldehydes, which undergo a Passerini reaction with carboxylic acids and isocyanides to produce the corresponding α-acyloxyamides in excellent yields.
Ehsan Sheikhi, Mehdi Adib
exaly   +2 more sources

Homologation of Ugi and Passerini reactions using ynamides

Drug Discovery Today: Technologies, 2018
Being important biological and pharmacological units, β-amino amides and β-acyloxy amides have a privileged position in both academia and industry. Developing a methods to prepare them has gained attention. Ynamides, which possess dual nucleophilic and electrophilic properties, are similar to isonitriles. In this review, usage of ynamides in the single
Bo, Huang, Sunliang, Cui
openaire   +2 more sources

An intramolecular passerini reaction: Synthesis of hydrastine.

Tetrahedron Letters, 1981
Abstract An intramolecular Passerini reaction between 3,4-methylenedioxyphenethylisocyanide and opianic acid is applied in a total synthesis of hydrastine, a phthalideisoquinoline alkaloid.
J.R. Falck, Sukumar Manna
openaire   +1 more source

Cationic lipids via multi-component Passerini reaction for non-viral gene delivery

New Journal of Chemistry
Lipid Nanoparticles (LNPs) are the most advanced non-viral platform for nucleic acid delivery, holding enormous potential applications in clinical therapy.
Rong Wang   +6 more
semanticscholar   +1 more source

FormylBODIPYs: Privileged Building Blocks for Multicomponent Reactions. The Case of the Passerini Reaction.

The Journal of Organic Chemistry, 2016
Eleven formyl-containing BODIPY dyes were prepared by means of either the Liebeskind-Srogl cross-coupling reaction or the Vilsmeier reaction. These dyes were used as components in the Passerini reaction to give highly substituted BODIPY dyes. A joined spectroscopic and theoretical characterization of the synthesized compounds was conducted to unravel ...
Diana E Ramírez-Ornelas   +7 more
semanticscholar   +3 more sources

Bioinspired Synthesis of the Central Core of Halichonadin H: The Passerini Reaction in a Hypothetical Biosynthesis of Marine Natural Products

Synthesis, 2019
A pathway is proposed for the biosynthesis of the unique homodimeric terpene, halichonadin H. The proposed biosynthetic pathway involves two key Passerini reactions of eudesmane-type terpene isocyanides.
Y. Ichikawa   +5 more
semanticscholar   +1 more source

Facile Synthesis and Properties of Multifunctionalized Polyesters by Passerini Reaction as Thermosensitive, Biocompatible, and Triggerable Drug Release Carriers.

ACS Applied Bio Materials, 2019
We developed a facile synthesis for a series of multifunctionalized polyesters by Passerini three-component polymerization (Passerini-3CP) in a "one-pot" method at room temperature using serial dicarboxylic acids, dialdehyde, and tert-butyl isocyanide as
Man Zhao   +6 more
semanticscholar   +1 more source

ChemInform Abstract: Regioselective Passerini and Passerini—Knoevenagel Reactions with vic‐Diketo Amides.

ChemInform, 2014
AbstractVicinal diketo amides react with isonitriles and carboxylic acids to α‐acyloxy β‐keto carboxamides.
Jan Rossbach, Klaus Harms, Ulrich Koert
openaire   +1 more source

Regioselective Passerini and Passerini–Knoevenagel Reactions with vic‐Diketo Amides

European Journal of Organic Chemistry, 2013
AbstractThe Passerini reaction of vic‐diketo amides with a variety of isocyanides and carboxylic acids has been examined. α‐Acyloxy β‐keto carboxamides were formed regioselectively as the major products. For the Passerini reactions with electron‐withdrawing‐group‐substituted acetic acids, a one‐pot Passerini–Knoevenagel reaction was accomplished by the
Jan Roßbach, Klaus Harms, Ulrich Koert
openaire   +1 more source

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