Results 51 to 60 of about 1,059 (165)

Insertion of Nitriles Into a Gold(III)/Carbene Bond: A Direct and Powerful Entry to Imino‐Substituted Carbenes

open access: yesAngewandte Chemie, Volume 137, Issue 23, June 2, 2025.
Stable imino‐substituted Au(III) carbenes are easily and efficiently prepared by trapping the transient (N^C^C)Au←:CH(dmp)+ carbene with nitriles. The corresponding free species are readily generated and display dual carbene / nitrile‐ylide reactivities. The diazo decomposition, nitrile insertion, and carbene transfer can be combined in three‐component
Rui Wei   +4 more
wiley   +2 more sources

Addition and cycloaddition reactions of Phosphinyl- and Phosphonyl-2H-Azirines, Nitrosoalkenes and Azoalkenes [PDF]

open access: yes, 2012
An overview of the use of 2H-azirines, conjugated nitrosoalkenes and conjugated azoalkenes bearing phosphorus substituents in addition and cycloaddition reactions is presented, focused on strategies for the synthesis of aminophosphonate and ...
Lemos, A.
core  

1,1‐Disubstituted Vinylbromides: Versatile Building Blocks for the Synthesis of Nitrogen‐Containing Heterocycles

open access: yesEuropean Journal of Organic Chemistry, EarlyView.
1,1‐Disubstituted vinylbromides are key intermediates for constructing nitrogen‐containing heterocycles. This review provides an overview of the synthetic applications of 1,1‐disubstituted vinylbromides and summarizes recent developments in reaction methodologies, mechanistic insights, and the structural diversity of N‐heterocyclic compounds accessible
Anne Westermeyer   +6 more
wiley   +1 more source

Composite Single‐Reference and Explicitly Correlated Multireference Calculations on the Mechanism of Pyrrole Pyrolysis

open access: yesJournal of Physical Organic Chemistry, Volume 39, Issue 4, April 2026.
New calculations have been applied to the pyrolysis of pyrrole under shock‐tube conditions and to the radical‐radical reaction between allyl and •CN at low temperature and pressure, using the same mechanistic scheme for both. ABSTRACT The pyrolysis of pyrrole has previously been studied in shock‐tube experiments and in jet‐stirred reactors. The results
Barry K. Carpenter
wiley   +1 more source

Cycloaddition reactions of conjugated azoalkenes [PDF]

open access: yes, 2012
An overview of the use of 2H-azirines, conjugated nitrosoalkenes and conjugated azoalkenes bearing phosphorus substituents in addition and cycloaddition reactions is presented, focused on strategies for the synthesis of aminophosphonate and ...
Lemos, A.
core  

Diels-alder cycloaddition of 2-azadienes to methyl 2-(2,6-dichlorophenyl)-2H-azirine-3-carboxylate in the synthesis of methyl 4-oxo-1,3-diazabicyclo[4.1.0]heptane-6-carboxylates [PDF]

open access: yes, 2004
A number of fused 4-oxo-1,3-diazabicyclo[4.1.0]heptane-6-carboxylates, a new type of compound, have been obtained by Diels-Alder cycloaddition between nucleophilic 2-azadienes and an electrophilic 2H-azirine.
Alves, M. José   +2 more
core   +1 more source

Recent Contributions of Organic Synthesis to Forensic Science

open access: yesChemPlusChem, Volume 91, Issue 2, February 2026.
Forensic science is a multidisciplinary field that plays a vital role in providing scientific evidence for criminal investigations. This review highlights advances and opportunities at the interface between organic synthesis and forensic science, with applications in drug identification, forensic toxicology, and latent fingerprint detection and ...
Gustavo dos Santos Martins   +3 more
wiley   +1 more source

Diseño y evaluación de nuevos derivados de aziridinas fosforadas como agentes [PDF]

open access: yes, 2021
418 p.Esta Tesis Doctoral, tiene como objetivo principal la síntesis de nuevos derivados de aziridina fosforados y su estudio como agentes antiproliferativos.
Carramiñana Jiménez, Víctor
core   +2 more sources

Investigation on the reactivity of α-azidochalcones with carboxylic acids: Formation of α-amido-1,3-diketones and highly substituted 2-(trifluoromethyl)oxazoles

open access: yesBeilstein Journal of Organic Chemistry, 2015
The reaction of α-azidochalcones with carboxylic acids has been investigated resulting in the formation of α-amido-1,3-diketones under microwave irradiation via in situ formation of 2H-azirine intermediates.
Kandasamy Rajaguru   +4 more
doaj   +1 more source

Síntese e reactividade de 2H - Azirinas [PDF]

open access: yes, 2007
Tese de Doutoramento em Ciências (Área de Especialização em Química Orgânica)O trabalho teve como objectivo primeiro, sintetizar 2H-azirinas com o grupo sulfinilo na posição 3.
Sousa, João Henriques de
core  

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