scholarly journals Correction to “Iridium-Catalyzed Highly Efficient and Site-Selective Deoxygenation of Alcohols”

ACS Catalysis ◽  
2021 ◽  
pp. 10478-10478
Author(s):  
Shiyi Yang ◽  
Weiping Tang ◽  
Zhanhui Yang ◽  
Jiaxi Xu
Keyword(s):  
Highly Efficient ◽  
Site Selective ◽  
Selective Deoxygenation

Iridium-Catalyzed Highly Efficient and Site-Selective Deoxygenation of Alcohols

ACS Catalysis ◽  
2018 ◽  
Vol 8 (10) ◽  
pp. 9320-9326 ◽  
Author(s):  
Shiyi Yang ◽  
Weiping Tang ◽  
Zhanhui Yang ◽  
Jiaxi Xu
Keyword(s):  
Highly Efficient ◽  
Site Selective ◽  
Selective Deoxygenation

scholarly journals Combination of inverse electron-demand Diels–Alder reaction with highly efficient oxime ligation expands the toolbox of site-selective peptide conjugations

2015 ◽  
Vol 51 (55) ◽  
pp. 11130-11133 ◽  
Author(s):  
S. Hörner ◽  
C. Uth ◽  
O. Avrutina ◽  
H. Frauendorf ◽  
M. Wiessler ◽  
...  
Keyword(s):  
Alder Reaction ◽  
Diels Alder ◽  
Inverse Electron Demand ◽  
Highly Efficient ◽  
Diels Alder Reaction ◽  
Site Selective ◽  
Electron Demand

A modular bioconjugation strategy based on stepwise oxime ligation and inverse electron-demand Diels–Alder reaction.

Differential formation of nitrogen-centered radicals leading to unprecedented, regioselective bromination of N,N′-(1,2-phenylene)bisamides and 2-amidophenols

2020 ◽  
Vol 7 (9) ◽  
pp. 1095-1106
Author(s):  
Damoder Reddy Motati ◽  
Dilipkumar Uredi ◽  
Amarender Goud Burra ◽  
J. Phillip Bowen ◽  
Frank R. Fronczek ◽  
...  
Keyword(s):  
Visible Light ◽  
Highly Efficient ◽  
Site Selective

A highly efficient, site-selective, visible light-accelerated, remote C–H halogenation of unsymmetrical aromatic bisamides/amidoesters has been developed.

scholarly journals meta-Oligoazobiphenyls – synthesis via site-selective Mills reaction and photochemical properties

2012 ◽  
Vol 8 ◽  
pp. 877-883 ◽  
Author(s):  
Raphael Reuter ◽  
Hermann A Wegner
Keyword(s):  
Cross Coupling ◽  
Structural Similarity ◽  
Point Of View ◽  
Azo Compounds ◽  
Photochromic Compounds ◽  
Highly Efficient ◽  
High Structural Similarity ◽  
Photochemical Properties ◽  
Novel Strategy ◽  
Site Selective

The investigation of multi-photochromic compounds constitutes a great challenge, not only from a synthetic point of view, but also with respect to the analysis of the photochemical properties. In this context we designed a novel strategy to access meta-oligoazobiphenyls via site-selective Mills reaction and Suzuki cross-coupling in a highly efficient iterative way. Photochemical examination of the resulting monomeric and oligomeric azo compounds revealed that the overall degree of switching was independent of the connected azo-units. However, one of the azobonds in the bis-azobiphenyl is isomerized preferentially despite the high structural similarity.

Selective functionalization of benzylic C-H bonds of two different benzylic ethers by bowl-shaped N-hydroxyimide derivatives as efficient organoradical catalysts

2022 ◽  
Author(s):  
Terumasa Kato ◽  
Keiji Maruoka
Keyword(s):  
Highly Efficient ◽  
Selective Functionalization ◽  
Synthetic Utility ◽  
Benzylic Ether ◽  
Diethyl Azodicarboxylate ◽  
Site Selective

A highly efficient, site-selective benzylic C-H bond amination of two different benzylic ether substrates was described by using bowl-shaped N-hydroxyimide organoradical catalysts with diethyl azodicarboxylate. The synthetic utility of this...

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