Results 151 to 160 of about 25,864 (264)
Isotelluroureas allow for the use of alkynoates for asymmetric (4+2)‐heterocycloadditions with different Michael acceptors. Alk‐2‐ynoates are readily available starting materials which, in principle, can be utilized for cycloadditions in analogy to structurally similar allenoates.
Anna Scheucher, Mario Waser
wiley +1 more source
A Free N-Heterocyclic Carbene and Its Metal Complex. [PDF]
Das A +9 more
europepmc +1 more source
Masked Silylenes: Controlled Generation and Reactivity Under Thermal and Equilibrium Conditions
This Review provides an overview of masked silylenes as bench‐stable precursors that release silylenes (R2Si:) under thermal activation or reversible equilibria. Precursor preparation, generation pathways, and characteristic reactivity are summarized, including trapping chemistry, reversible interconversions, insertion‐type processes, and small ...
Kei Ota, Kanata Miyahara, Norio Nakata
wiley +1 more source
1,1‐and 1,2‐Diborylalkenes: Preparation and Synthetic Applications
In this review, we highlight recent advances in the synthesis and reactivity of 1,1‐diborylalkenes and 1,2‐diborylalkenes, along with various transformations leading to C‐C, C‐heteroatom, and multicomponent products. By providing a comprehensive and practical resource, this review aims to assist researchers in exploring the synthetic utility of 1,1 and
Jayaram Vankudoth +2 more
wiley +1 more source
Advances in Catalysis Using N-Heterocyclic Carbene Platinum Complexes. [PDF]
Smoczyńska A +2 more
europepmc +1 more source
Visible light activates β‐aryl α,β‐unsaturated acylsilanes to form indenols without catalysts or metals. A stepwise photochemical cascade reorganizes simple precursors through isomerization, rearrangement, and ring formation. The process highlights sustainable reaction design while showcasing the synthetic power of acylsilane photochemistry and the ...
Adrián Álvarez +4 more
wiley +1 more source
Iodine‐Mediated Electrochemical Diastereoselective Synthesis of Enaminones
This work describes an efficient electrochemical (EC) method for transforming thioamides into enaminones via reaction with organic diazo compounds. The electrochemical approach is cost‐effective, mild, and proceeds through the in situ electrochemical generation of a copper complex.
Ijaz Khan +2 more
wiley +1 more source
N‑Heterocyclic Carbene Stabilized Aluminum Alkyls and Their Reactivity toward NHC-Alanes. [PDF]
Burnett S, Kennedy AR, Weetman CE.
europepmc +1 more source
Redox‐active guanidines, comprising guanidino‐functionalized aromatics (GFAs) and redox‐active urea azines (RAAs), are electron donors and strong Lewis and Brønsted bases that are used in several applications. They act as redox‐active ligands in bistable coordination compounds and as reagents in dehydrogenative coupling reactions and proton‐coupled ...
Hans‐Jörg Himmel
wiley +1 more source
N-Heterocyclic Carbene Stabilized Bisacylgermylenes. [PDF]
Paris M +3 more
europepmc +1 more source

