Late transition metal-catalyzed hydroamination and hydroamidation
L Huang, M Arndt, K Gooßen, H Heydt… - Chemical …, 2015 - ACS Publications
This Review examines recent developments in late transition metal-catalyzed
hydroamination and-amidation reactions. A hydroamination is a reaction in which an N− H …
hydroamination and-amidation reactions. A hydroamination is a reaction in which an N− H …
Advances of azide-alkyne cycloaddition-click chemistry over the recent decade
During the past years, a variety of scientific and methodological developments have been
achieved, which urge chemists to increase the tools of their arsenal to improve the ease and …
achieved, which urge chemists to increase the tools of their arsenal to improve the ease and …
Aza-Michael reaction: achievements and prospects
AY Rulev - Russian Chemical Reviews, 2011 - iopscience.iop.org
Data published in the last 10 years on the use of the aza-Michael reaction in organic
synthesis are described systematically. The attention is focused on environmentally friendly …
synthesis are described systematically. The attention is focused on environmentally friendly …
Multicomponent Syntheses based upon Copper‐Catalyzed Alkyne‐Azide Cycloaddition
S Hassan, TJJ Mueller - Advanced Synthesis & Catalysis, 2015 - Wiley Online Library
The copper‐catalyzed alkyne‐azide cycloaddition (CuAAC) is a highly versatile,
regioselective synthesis of 1, 4‐disubstituted 1, 2, 3‐triazoles under mild reaction conditions …
regioselective synthesis of 1, 4‐disubstituted 1, 2, 3‐triazoles under mild reaction conditions …
Catalytic Asymmetric Synthesis of [2, 3]‐Fused Indoline Heterocycles through Inverse‐Electron‐Demand Aza‐Diels–Alder Reaction of Indoles with Azoalkenes
MC Tong, X Chen, J Li, R Huang, H Tao… - Angewandte …, 2014 - Wiley Online Library
An unprecedented catalytic asymmetric inverse‐electron‐demand aza‐Diels–Alder reaction
of indoles with in situ formed azoalkenes is reported. A diverse set of [2, 3]‐fused indoline …
of indoles with in situ formed azoalkenes is reported. A diverse set of [2, 3]‐fused indoline …
Recent advances in the chemistry of conjugated nitrosoalkenes and azoalkenes
This review aims to present the most recent contributions in the chemistry of nitrosoalkenes
and azoalkenes, highlighting the chemical behavior that makes them important and versatile …
and azoalkenes, highlighting the chemical behavior that makes them important and versatile …
I2/TBPB Mediated Oxidative Reaction of N-Tosylhydrazones with Anilines: Practical Construction of 1,4-Disubstituted 1,2,3-Triazoles under Metal-Free and Azide …
ZJ Cai, XM Lu, Y Zi, C Yang, LJ Shen, J Li… - Organic …, 2014 - ACS Publications
An efficient I2 (20 mol%)/TBPB mediated oxidative formal [4+ 1] cycloaddition of N-
tosylhydrazones with anilines via C–N/N–N bond formation and S–N cleavage has been …
tosylhydrazones with anilines via C–N/N–N bond formation and S–N cleavage has been …
Catalytic [2, 3]-sigmatropic rearrangement of sulfonium ylides derived from azoalkenes: non-carbenoid Doyle–Kirmse reaction
FY Yang, TJ Han, SK Jia, MC Wang… - Chemical …, 2023 - pubs.rsc.org
The Sc (III)-catalyzed [2, 3]-sigmatropic rearrangement of sulfonium ylides derived from
azoalkenes has been established. Owing to the absence of a carbenoid intermediate, this …
azoalkenes has been established. Owing to the absence of a carbenoid intermediate, this …
Experimental evidence for the involvement of dinuclear alkynylcopper (I) complexes in alkyne–azide chemistry
Dinuclear alkynylcopper (I) ladderane complexes are prepared by a robust and simple
protocol involving the reduction of Cu2 (OH) 3OAc or Cu (OAc) 2 by easily oxidised alcohols …
protocol involving the reduction of Cu2 (OH) 3OAc or Cu (OAc) 2 by easily oxidised alcohols …
TEMPO-mediated aza-Diels–Alder reaction: Synthesis of tetrahydropyridazines using ketohydrazones and olefins
XL Yang, XX Peng, F Chen, B Han - Organic letters, 2016 - ACS Publications
A novel, facile, and efficient method for the synthesis of tetrahydropyridazines by a one-pot
tandem reaction of easily accessible ketohydrazones and olefins in the presence of 2, 2, 6, 6 …
tandem reaction of easily accessible ketohydrazones and olefins in the presence of 2, 2, 6, 6 …