Results 11 to 20 of about 754 (188)

Enantioselective Synthesis of Spiroindenes by Enol-Directed Rhodium(III)-Catalyzed C-H Functionalization and Spiroannulation. [PDF]

open access: bronzeAngew Chem Int Ed Engl, 2015
Chirale Cp‐Rhodium‐Komplexe vermitteln die enantioselektive Enol‐dirigierte C(sp2)‐H‐Funktionalisierung und oxidative Anellierung mit Alkinen unter Bildung von Spiroindenen mit quartären Kohlenstoff‐Stereozentren. Entscheidend für hohe ee‐Werte sind offenbar eine hohe Selektivität zwischen zwei dirigierenden Gruppen sowie die Kontrolle der ...
Reddy Chidipudi S   +3 more
europepmc   +7 more sources

Ruthenium‐Catalyzed Decarboxylative Rearrangement of 4‐Alkenyl‐isoxazol‐5‐ones to Pyrrole Derivatives [PDF]

open access: yesEuropean Journal of Organic Chemistry, Volume 2022, Issue 25, July 7, 2022., 2022
Easily accessible isoxazol‐5(4H)‐ones are useful precursors of different heterocycles. In this work, the ruthenium‐catalyzed transformation of 4‐alkenyl‐substituted isoxazol‐5‐ones to 1H‐pyrrole derivatives is reported. Abstract Easily accessible isoxazol‐5(4H)‐ones are useful precursors of heterocycles.
Letizia Molteni   +6 more
wiley   +3 more sources

Aniline Derivatives from Lignin under Mild Conditions Enabled by Electrochemistry [PDF]

open access: yesChemSusChem, Volume 17, Issue 3, February 8, 2024.
Electrochemical oxidation of lignin‐derived guaiacols & syringols leads to cyclohexadienone intermediates in moderate to good yields. These react with ethyl glycinate hydrochloride under mild conditions to afford lignin‐based anilines. This methodology can be incorporated to reductive catalytic fractionation processes towards selective obtention of 4 ...
Antonio A. Castillo‐Garcia   +3 more
wiley   +3 more sources

From Conventional to Sustainable Catalytic Approaches for Heterocycles Synthesis [PDF]

open access: yesChemSusChem, Volume 17, Issue 8, April 22, 2024.
Catalysed synthetic methods, such as transition metals, organocatalysts, photocatalysts, iodine‐catalysed reaction, electrochemical reactions and green innovative methods are of great interest for the sustainable synthesis of heterocyclic compounds, important building blocks for several applications.
Carla Rizzo   +4 more
wiley   +3 more sources

Diastereoselective spiroannulation of phenolic derivatives: Effect of steric hindrance on the diastereoselectivity. [PDF]

open access: gold, 2010
The objective of this study was to determine the effect, if any, that steric factors have on the oxidative spiroannulation of simple phenols bearing substituents that are increasing in size.
Lyndia M. Susag
openalex   +4 more sources

Stereoselective N ‐Heterocyclic‐Carbene‐Catalyzed Spiroannulation as an Access Towards Spirobenzofuranone‐Fused Cyclohexenones [PDF]

open access: hybridAdvanced Synthesis &Catalysis, Volume 366, Issue 24, Page 5008-5014, December 17, 2024.
Abstract In this work, we present an organocatalytic spiroannulation method that provides access to spirocyclic benzofuran‐2‐ones. The reaction proceeds via the generation of an azolium dienolate from an α‐bromo‐α,β‐unsaturated aldehyde using a chiral N‐heterocyclic carbene, followed by annulation with benzofuran‐2‐one‐derived alkenes.
Ladislav Lóška   +8 more
openalex   +2 more sources

Home - About - Disclaimer - Privacy