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A Theoretical Study on the Photochemical Isomerization of 2,6-Dimethylpyrazine

Maurizio D’Auria · Organics · 2022

DFT calculations on the photoisomerization of 2,6-dimethylpyrazine allowed us to confirm the role of benzvalene isomers in the isomerization of hexatomic heterocyclic compounds. 2,6-Dimethylpyrazine in the excited singlet states can be converted into the corresponding Dewar isome...

Open access Research Article 10.3390/org3020007

Stabilized Arylzinc Iodides in Negishi Acylative Cross-Coupling: A Modular Synthesis of Chalcones

Michele Pierigé, Anna Iuliano, Gaetano Angelici & Gianluca Casotti · Organics · 2022

Stabilized arylzinc iodides, synthesized by direct insertion of zinc into the corresponding halides, were used as nucleophiles into an acylative Negishi coupling reaction to synthesize chalcones. The reaction conditions were optimized to afford optimal results on a model reaction...

Open access Research Article 10.3390/org3020006

β-Cyclodextrin Supramolecular Recognition of bis-Cationic Dithienylethenes

Giulio Bianchini, Mattia Bazan, Fabrizio Fabris & Alessandro Scarso · Organics · 2022

The supramolecular interactions in water between β-cyclodextrin and the open and closed photochromic forms of two bis-cationic dithienylethenes, characterized by different electronic properties, were investigated aiming at underlying the key aspects of the recognition process. Th...

Open access Research Article 10.3390/org3020005

On the Mechanism of the Synthesis of Nitrofunctionalised Δ2-Pyrazolines via [3+2] Cycloaddition Reactions between α-EWG-Activated Nitroethenes and Nitrylimine TAC Systems

Agnieszka Fryźlewicz, Aleksandra Olszewska, Karolina Zawadzińska, Przemysław Woliński, Karolina Kula, Agnieszka Kącka-Zych, Agnieszka Łapczuk-Krygier & Radomir Jasiński · Organics · 2022

We investigated the reactivity of different substituted nitrylimine-type three atom components (TACs) in [3+2] cycloaddition (32CAs) reactions with electrophilically activated nitroethenes within molecular electron density theory (MEDT). In parallel research, the molecular mechan...

Open access Research Article 10.3390/org3010004

13C NMR Spectroscopic Studies of Intra- and Intermolecular Interactions of Amino Acid Derivatives and Peptide Derivatives in Solutions

Yoshikazu Hiraga, Saori Chaki, Yuri Uyama, Ryosuke Hoshide, Takumi Karaki, Daisuke Nagata, Kanji Yoshimoto & Satomi Niwayama · Organics · 2022

13C NMR spectroscopic investigations were conducted for various amino acid derivatives and peptides. It was observed that 13C NMR chemical shifts of the carbonyl carbons are correlated with the solvent polarities, but the extent depends on the structures. The size of the function...

Open access Research Article 10.3390/org3010003

Micellar Suzuki Cross-Coupling between Thiophene and Aniline in Water and under Air

Dawod Yousif, Silvia Tombolato, Elmehdi Ould Maina, Riccardo Po, Paolo Biagini, Antonio Papagni & Luca Vaghi · Organics · 2021

The Suzuki–Miyaura cross-coupling reaction plays a fundamental role in modern synthetic organic chemistry, both in academia and industry. For this reason, scientists continue to search for new, more effective, cheaper and environmentally friendly procedures. Recently, micellar sy...

Open access Research Article 10.3390/org2040025

1-(4-Nitrophenyl)-1H-1,2,3-Triazole-4-carbaldehyde: Scalable Synthesis and Its Use in the Preparation of 1-Alkyl-4-Formyl-1,2,3-triazoles

Tomas Opsomer, Kaat Valkeneers, Ana Ratković & Wim Dehaen · Organics · 2021

1,2,3-Triazole-4-carbaldehydes are useful synthetic intermediates which may play an important role in the discovery of novel applications of the 1,2,3-triazole moiety. In this work, a one-step multigram scale synthesis of 4-formyl-1-(4-nitrophenyl)-1H-1,2,3-triazole (FNPT) as a p...

Open access Research Article 10.3390/org2040024

Primary Phosphines and Phosphine Oxides with a Stereogenic Carbon Center Adjacent to the Phosphorus Atom: Synthesis and Anti-Markovnikov Radical Addition to Alkenes

Toshiaki Murai, Ryota Wada, Kouji Iwata, Yuuki Maekawa, Kazuma Kuwabara & Mao Minoura · Organics · 2021

Organophosphorus compounds with stereogenic phosphorus and carbon atoms have received increasing attention. In this regards, primary phosphines with a stereogenic carbon atom adjacent to the phosphorus atom were synthesized by the reduction in phosphonates and phosphonoselenoates...

Open access Research Article 10.3390/org2040023

Boranils: Versatile Multifunctional Organic Fluorophores for Innovative Applications

Julien Massue, Denis Jacquemin & Gilles Ulrich · Organics · 2021

Multifunctional stimuli-responsive fluorophores showing bright environment-sensitive emissions have fueled intense research due to their innovative applications in the fields of biotechnologies, optoelectronics, and materials. A strong structural diversity is observed among molec...

Open access Research Article 10.3390/org2040020

Recent Advances in the Synthesis of Piperazines: Focus on C–H Functionalization

Carolina Durand & Michal Szostak · Organics · 2021

Piperazine ranks as the third most common nitrogen heterocycle in drug discovery, and it is the key component of several blockbuster drugs, such as Imatinib (also marketed as Gleevec) or Sildenafil, sold as Viagra. Despite its wide use in medicinal chemistry, the structural diver...

Open access Research Article 10.3390/org2040018

Synthesis of 1-Trifluorometylindanes and Close Structures: A Mini Review

Olesya V. Khoroshilova & Aleksander V. Vasilyev · Organics · 2021

This review describes methods for the synthesis of 1-trifluomethylindanes and close structures, which are still quite rare and scarcely available compounds. There are two main approaches to obtain 1-CF3-indanes. The first one is the construction of an indane system from CF3 precu...

Open access Research Article 10.3390/org2040019

Electrocyclizations of Conjugated Azapolyenes Produced in Reactions of Azaheterocycles with Metal Carbenes

Nikolai V. Rostovskii, Mikhail S. Novikov & Alexander F. Khlebnikov · Organics · 2021

Conjugated azapolyenes (azabuta-1,3-dienes, aza-/diaza-/oxaza-/oxadiazahexa-1,3,5-trienes) are highly reactive in electrocyclization reactions, which makes them convenient precursors for the synthesis of a wide range of four-, five-, and six-membered nitrogen heterocycles that ar...

Open access Research Article 10.3390/org2030017

Synthesis of Illisimonin a Skeleton by Intramolecular Diels–Alder Reaction of Ortho-Benzoquinones and Biomimetic Skeletal Rearrangement of Allo-Cedranes

Takahiro Suzuki, Riko Nagahama, Muhammad Aiman Fariz, Yuki Yukutake, Kazutada Ikeuchi & Keiji Tanino · Organics · 2021

Illisimonin A is a new sesquiterpene isolated from Illicium simonsii, and it possesses a novel 5/5/5/5/5 pentacyclic skeleton. The tricyclic skeleton of illisimonin A, tricyclo[5.2.1.01,5]decane, is presumed to be biosynthesized from allo-cedranes via a skeletal rearrangement. He...

Open access Research Article 10.3390/org2030016