Results 61 to 70 of about 2,363 (206)

1,3-Dipolar Cycloaddition of Azomethine Ylides to Aldehydes: Synthesis of anti α-Amino-β-Hydroxy Esters

, 2010
A 1,3-dipolar cycloaddition reaction of azomethine ylides to aldehydes is described. The azomethine ylides, generated by thermal electrocyclic ring opening of aziridines, adds to aldehydes in good yields with moderate to good selectivities to furnish ...
Lauri Toom, Danielsson, Jakob,, Peter Somfai, Somfai, Peter,, Toom, Lauri,, Jakob Danielsson   +5 more
core   +1 more source

Benzotriazolylmethylaminosilanes: Novel azomethine ylide equivalents

Tetrahedron, 1994
Abstract Benzotriazolylmethylaminosilanes, readily accessible from the reaction of benzotriazole, an aldehyde and an (aminomethyl)silane in water at 20°C, are azomethine ylide equivalents which undergo stereospecific cycloadditions with dipolarophiles to give substituted pyrrolidines or 2,5-dihydropyrroles in good yields.
Center for Heterocyclic Compounds, Department of Chemistry, University of Florida, FL 32611-7200 USA ( host institution ), R. Katritzky, Alan, Köditz, Jens, Lang, Hengyuan   +3 more
openaire   +2 more sources

Heat‐Induced Toxicants: Sensory Appeal Distracts Consumers' Attention From Potential Toxicological Risks of Thermally Processed Foods

Food Science &Nutrition, Volume 14, Issue 4, April 2026.
The central paradox of thermal processing of foods. (A) The application of heat (e.g., frying, baking, grilling) to food initiates complex chemical reactions, most notably the Maillard reaction and thermal degradation of protein, lipids, and carbohydrate. (B) These reactions create a desirable sensory experience characterized by enticing aromas, golden‐
Joachim Dotto Matondo, Abdulsudi Issa‐Zacharia   +1 more
wiley   +1 more source

Stereocontrolled 1,3-dipolar cycloadditions using Oppolzer's camphor sultam as the chiral auxiliary for carbonyl stabilized azomethine ylides

, 2001
Two complementary approaches to substituted pyrrolidines via stereocontrolled 1,3-dipolar cycloaddition reactions of chiral azomethine ylides are described.
Wiley J. Youngs, John Protasiewicz, Rebecca Zaniewski, Philip Garner, Özdemir Dogan, Vance O. Kennedy, Vance, Kennedy, Doğan, Özdemir, Garner, Philip, Protasiewicz, John, Zaniewski, Rebecca, Youngs, Wiley   +11 more
core   +1 more source

azomethine ylides

, 2008
Citation: 'azomethine ylides' in the IUPAC Compendium of Chemical Terminology, 3rd ed.; International Union of Pure and Applied Chemistry; 2006. Online version 3.0.1, 2019. 10.1351/goldbook.A00565 • License: The IUPAC Gold Book is licensed under Creative Commons Attribution-ShareAlike CC BY-SA 4.0 International for individual terms.
openaire   +1 more source

Bis‐Furans: A Sustainable Source of Diverse Molecular Architectures

European Journal of Organic Chemistry, Volume 29, Issue 10, 9 March 2026.
A concise synthetic route to diverse acyclic and heterocyclic compounds has been developed by combining hetero‐Diels–Alder reactions, DBU‐promoted ring openings, and Lewis base‐catalyzed annulations. Nitrosoalkenes reacted with furan derivatives to form 4a,7a‐dihydro‐4H‐furo[2,3‐e][1,2]oxazines, which underwent DBU‐promoted rearrangements to 6H‐1,2 ...
Ana L. Cardoso, José A. Paixão, Teresa M. V. D. Pinho e Melo   +2 more
wiley   +1 more source

Nano‐ and Micro‐Sized Solid Materials Used as Antiviral Agents

Advanced Functional Materials, Volume 36, Issue 26, 30 March 2026.
Due to the rise of viral infections in humans and possible viral outbreaks, the use of nano‐ or micro‐sized materials as antiviral agents is rapidly increasing. This review explores their antiviral properties against RNA and DNA viruses, either as a prevention or a treatment tool, by delving into their mechanisms of action and how to properly assess ...
Orfeas‐Evangelos Plastiras, Imelda Raczkiewicz, Peggy Bouquet, Jean‐Philippe Dacquin, Jeremy Dhainaut, Anne Goffard, Christophe Volkringer   +6 more
wiley   +1 more source

Intramolecular Cycloaddition Azomethine Ylides and α-(Trifluoromethyl)styrenes as Dipolarophiles

, 2019
The synthesis of polycyclic fluorinated tertiary amines has been accomplished by means of an intramolecular azomethine ylide cycloaddition with fluorinated dipolarophiles. Thus, tri- and tetracyclic fused pyrrolidines bearing a quaternary trifluoromethyl
Sánchez Merino, Anabel, Gavina, Daniel, Anabel Sánchez Merino, Daniel Gaviña, Delgado, Alejandro, Sánchez Roselló, María, Rabasa Alcañiz, Fernando, Carlos del Pozo, María Sánchez Roselló, del Pozo Losada, Carlos, Fernando Rabasa Alcañiz, Alejandro Delgado   +11 more
core   +1 more source

An effective one-pot access to polynuclear dispiroheterocyclic structures comprising pyrrolidinyloxindole and imidazothiazolotriazine moieties via a 1,3-dipolar cycloaddition strategy

Beilstein Journal of Organic Chemistry, 2016
An effective and highly regio- and diastereoselective one-pot method for the synthesis of new polynuclear dispiroheterocyclic systems with five stereogenic centers (dispiro[imidazo[4,5-e]thiazolo[3,2-b]-1,2,4-triazine-6,3′-pyrrolidine-2′,3′′-indoles ...
Alexei N. Izmest’ev, Galina A. Gazieva, Natalya V. Sigay, Sergei A. Serkov, Valentina A. Karnoukhova, Vadim V. Kachala, Alexander S. Shashkov, Igor E. Zanin, Angelina N. Kravchenko, Nina N. Makhova   +9 more
doaj   +1 more source

Synthesis of bis-spirocyclic derivatives of 3-azabicyclo[3.1.0]hexane via cyclopropene cycloadditions to the stable azomethine ylide derived from Ruhemann's purple

Beilstein Journal of Organic Chemistry, 2022
A reliable method for the synthesis of bis-spirocyclic derivatives of 3-azabicyclo[3.1.0]hexanes through the 1,3-dipolar cycloaddition (1,3-DC) reactions of cyclopropenes to the stable azomethine ylide – protonated form of Ruhemann's purple (PRP) has ...
Alexander S. Filatov, Olesya V. Khoroshilova, Anna G. Larina, Vitali M. Boitsov, Alexander V. Stepakov   +4 more
doaj   +1 more source