Metal-free intramolecular amino-acyloxylation of 2-aminostyrene with carboxylic acid for the synthesis of 3-acyloxyl indolines in water

2017 ◽  
Vol 19 (9) ◽  
pp. 2076-2079 ◽  
Author(s):  
Liyan Liu ◽  
Zhiyong Wang

A metal-free amino-acyloxylation of 2-aminostyrene was developed for the synthesis of 3-acyloxyl indolines.

2021 ◽  
Author(s):  
Mu-Jia Luo ◽  
Gui-Fen Lv ◽  
Yang Li ◽  
Jin-Heng Li

Metal-free amino-assisted electrochemical intramolecular C–O or C–N couplings of amino-2-(2-aminoaryl)phenols are described.


2019 ◽  
Author(s):  
Yiru Zhang ◽  
Jianlei Shen ◽  
Rong Hu ◽  
Shi Xiujuan ◽  
Xianglong Hu ◽  
...  

In this work, we use a spontaneous and catalyst-free amino-yne click bioconjugation to generate activated ethynyl group functionalized surfaces for fast immobilizing native proteins and cells. Biomolecules, such as bovine serum albumin (BSA), human IgG and peptide of C(RGDfK), could be covalently immobilized on the surfaces in as short as 30 min. Notably, the bioactivity of the anchored biomolecules remain intact, which is verified by efficiently capturing target antibodies and cells from the bulk solutions. This strategy represents an alternative for highly efficient surface biofunctionalization.


2020 ◽  
Author(s):  
Alexandra Millimaci ◽  
Rowan Meador ◽  
Sara Dampf ◽  
John D. Chisholm

<div> <div> <div> <p>4-Acetamido-2,2,6,6-tetramethyl-1-oxopiperidinium tetrafluoroborate (Bobbitt’s salt) effectively activates electron rich alkenes and promotes the addition of anilines. This transformation provides a direct, transition metal free method for amino-oxidation of alkenes under mild conditions. The relative stereochemistry of the amino-oxidation is influenced by solvent effects, with both the syn and anti amino-oxidation products being accessible from identical starting materials. </p> </div> </div> </div>


2013 ◽  
Vol 15 (17) ◽  
pp. 4552-4555 ◽  
Author(s):  
Lovely Angel Panamparambil Antony ◽  
Tomáš Slanina ◽  
Peter Šebej ◽  
Tomáš Šolomek ◽  
Petr Klán

2006 ◽  
Vol 10 (02) ◽  
pp. 122-131 ◽  
Author(s):  
Zbynek Musil ◽  
Petr Zimcik ◽  
Miroslav Miletin ◽  
Kamil Kopecky ◽  
Marek Link ◽  
...  

New metal-free, magnesium and zinc azaphthalocyanines ( AzaPc ) were prepared from 6-(3-tert-butylsulfany1-5,6-dicyanopyrazine-2-ylamino)hexanoic acid and its butylester and N,N-diethylamide. Their singlet oxygen production was measured by a dye-sensitized photooxidation of 1,3-diphenylisobenzofuran ( DPBF ) and ΦΔ values were calculated. It was found that the presence of carboxylic acid in the structure of AzaPc decreases their singlet oxygen production. Singlet oxygen activity of the newly prepared compounds (containing mixed alkylamino and alkylsulfanyl peripheral substituents) lies between purely alkylsulfanyl and alkylamino derivatives of AzaPc . This fact further supports previously proposed structure-activity relationships, where alkylsulfanyl derivatives belong to the best singlet oxygen producers while the presence of alkylamino substituents in the structure rapidly decreases their photodynamic properties.


2016 ◽  
Vol 14 (40) ◽  
pp. 9485-9489 ◽  
Author(s):  
Navanita T. Thirumoorthi ◽  
Vikrant A. Adsool

As a part of our ongoing synthetic quest to expand the frontiers of contemporary medicinal chemistry, we now report an expedient synthesis of a potentially useful bicyclo[1.1.1]pentane building block, 3-(pyrazin-2-yl)bicyclo[1.1.1]pentane-1-carboxylic acid. This report also showcases the application of this motif as a “spacer” probe in a biological study.


2017 ◽  
Vol 359 (20) ◽  
pp. 3503-3508 ◽  
Author(s):  
Toshifumi Dohi ◽  
Daichi Koseki ◽  
Kohei Sumida ◽  
Kana Okada ◽  
Serina Mizuno ◽  
...  
Keyword(s):  

Heterocycles ◽  
2015 ◽  
Vol 91 (9) ◽  
pp. 1723 ◽  
Author(s):  
Ning Zhu ◽  
Guangyan Du ◽  
Limin Han ◽  
Hailong Hong ◽  
Quanling Suo

2020 ◽  
Vol 56 (20) ◽  
pp. 3073-3076 ◽  
Author(s):  
Francesca Franco ◽  
Sara Meninno ◽  
Maurizio Benaglia ◽  
Alessandra Lattanzi

A direct and general one-pot approach to α-trifluoromethylthiolated amides, esters and carboxylic acids has been successfully developed under mild, catalytic and metal-free conditions.


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