A novel phosphoramidite for the site-selective introduction of functional groups into oligonucleotides via versatile tethers

1994 ◽  
Vol 35 (32) ◽  
pp. 5879-5882 ◽  
Author(s):  
Masayuki Endo ◽  
Yoshitaka Saga ◽  
Makoto Komiyama
Synthesis ◽  
2021 ◽  
Author(s):  
Buddhadeb Chattopadhyay ◽  
Mirja Md Mahamudul Hassan ◽  
Md Emdadul Hoque ◽  
Sayan Dey ◽  
Saikat Guria ◽  
...  

We report a convenient method for the highly site selective borylation of 8-arylquinoline. The reaction proceeds smoothly in presence of catalytic amount of [Ir(OMe)(cod)]2 and 2-phenylpyridine derived ligand using bis(pinacolato)diborane as the borylating agent. The reactions occur with high selectivity with many functional groups, providing a series of borylated 8-aryl quinolines with good to excellent yield and excellent selectivity. The borylated compounds formed in this method can be transformed to various important synthons using known transformations.


2020 ◽  
Vol 11 (1) ◽  
Author(s):  
Hua Tang ◽  
Yu-Biao Tian ◽  
Hongyan Cui ◽  
Ren-Zhe Li ◽  
Xia Zhang ◽  
...  

Abstract Site-selective modification of complex molecules allows for rapid accesses to their analogues and derivatives, and, therefore, offers highly valuable opportunities to probe their functions. However, to selectively manipulate one out of many repeatedly occurring functional groups within a substrate represents a grand challenge in chemistry. Yet more demanding is to develop methods in which alterations to the reaction conditions lead to switching of the specific site of reaction. We report herein the development of a Pd/Lewis acid co-catalytic system that achieves not only site-selective, but site-switchable mono-O-allylation of polyols with readily available reagents and catalysts. Through exchanging the Lewis acid additives that recognize specific hydroxyls in a polyol substrate, our system managed to install a versatile allyl group to the target in a site-switchable manner. Our design demonstrates remarkable scope, and is amenable to the direct derivatization of various complex, bioactive natural products.


2007 ◽  
Vol 46 (27) ◽  
pp. 5238-5241 ◽  
Author(s):  
Stephan Denifl ◽  
Philipp Sulzer ◽  
Dieter Huber ◽  
Fabio Zappa ◽  
Michael Probst ◽  
...  

2021 ◽  
pp. 131043
Author(s):  
Van-Thang Nguyen ◽  
Guralamatta Siddappa Ravi Kumara ◽  
Kashi Raj Bhattarai ◽  
Han–Jung Chae ◽  
Young Jun Seo

2019 ◽  
Vol 5 (1) ◽  
Author(s):  
Aung Thiha ◽  
Fatimah Ibrahim ◽  
Shalini Muniandy ◽  
Marc J. Madou

AbstractCarbon micro- and nanoelectrodes fabricated by carbon microelectromechanical systems (carbon MEMS) are increasingly used in various biosensors and supercapacitor applications. Surface modification of as-produced carbon electrodes with oxygen functional groups is sometimes necessary for biofunctionalization or to improve electrochemical properties. However, conventional surface treatment methods have a limited ability for selective targeting of parts of a surface area for surface modification without using complex photoresist masks. Here, we report microplasma direct writing as a simple, low-cost, and low-power technique for site-selective plasma patterning of carbon MEMS electrodes with oxygen functionalities. In microplasma direct writing, a high-voltage source generates a microplasma discharge between a microelectrode tip and a target surface held at atmospheric pressure. In our setup, water vapor acts as an ionic precursor for the carboxylation and hydroxylation of carbon surface atoms. Plasma direct writing increases the oxygen content of an SU-8-derived pyrolytic carbon surface from ~3 to 27% while reducing the carbon-to-oxygen ratio from 35 to 2.75. Specifically, a microplasma treatment increases the number of carbonyl, carboxylic, and hydroxyl functional groups with the largest increase observed for carboxylic functionalities. Furthermore, water microplasma direct writing improves the hydrophilicity and the electrochemical performance of carbon electrodes with a contact-angle change from ~90° to ~20°, a reduction in the anodic peak to cathodic peak separation from 0.5 V to 0.17 V, and a 5-fold increase in specific capacitance from 8.82 mF∙cm−2 to 46.64 mF∙cm−2. The plasma direct-writing technology provides an efficient and easy-to-implement method for the selective surface functionalization of carbon MEMS electrodes for electrochemical and biosensor applications.


2018 ◽  
Vol 16 (32) ◽  
pp. 5889-5898 ◽  
Author(s):  
Pinaki Bhusan De ◽  
Sonbidya Banerjee ◽  
Sourav Pradhan ◽  
Tharmalingam Punniyamurthy

Ruthenium-catalyzed site-selective C7-acyloxyation of indolines with carboxylic acids is presented that can be oxidized to indoles with diverse functional groups.


1971 ◽  
Author(s):  
Warren G. Bennis ◽  
Michael Beer ◽  
Gerald R. Pieters ◽  
Alan T. Hundert ◽  
Samuel H. Marcus ◽  
...  

2016 ◽  
Vol 19 (2) ◽  
pp. 93-100
Author(s):  
Lalita El Milla

Scaffolds is three dimensional structure that serves as a framework for bone growth. Natural materials are often used in synthesis of bone tissue engineering scaffolds with respect to compliance with the content of the human body. Among the materials used to make scafffold was hydroxyapatite, alginate and chitosan. Hydroxyapatite powder obtained by mixing phosphoric acid and calcium hydroxide, alginate powders extracted from brown algae and chitosan powder acetylated from crab. The purpose of this study was to examine the functional groups of hydroxyapatite, alginate and chitosan. The method used in this study was laboratory experimental using Fourier Transform Infrared (FTIR) spectroscopy for hydroxyapatite, alginate and chitosan powders. The results indicated the presence of functional groups PO43-, O-H and CO32- in hydroxyapatite. In alginate there were O-H, C=O, COOH and C-O-C functional groups, whereas in chitosan there were O-H, N-H, C=O, C-N, and C-O-C. It was concluded that the third material containing functional groups as found in humans that correspond to the scaffolds material in bone tissue engineering.


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