Site Selective Formation of Thymine Glycol-Containing Oligodeoxynucleotides by Oxidation with Osmium Tetroxide and Bipyridine-Tethered Oligonucleotide

2000 ◽  
Vol 122 (26) ◽  
pp. 6309-6310 ◽  
Author(s):  
Kazuhiko Nakatani ◽  
Shinya Hagihara ◽  
Shinsuke Sando ◽  
Hiroshi Miyazaki ◽  
Kazuhito Tanabe ◽  
...  
Keyword(s):  
Osmium Tetroxide ◽  
Thymine Glycol ◽  
Site Selective ◽  
Selective Formation

Tetrathiafulvalene-based nanocrystals: site-selective formation, device fabrication, and electrical properties

2015 ◽  
Vol 3 (34) ◽  
pp. 8986-8991 ◽  
Author(s):  
Hiroyuki Hasegawa
Keyword(s):  
Electrical Properties ◽  
Device Fabrication ◽  
Site Selective ◽  
Selective Formation

A tetrathiafulvalene (TTF)-based nanocrystal was selectively synthesized only in the gap between two electrodes using a nanoscale electrocrystallization. A two-terminal TTF-based device and an FET could be readily obtained via an eco-friendly nanofabrication process.

Templating nanotraffic light – dynamic tricoloured blinking silver nanoclusters on a graphene oxide film

2018 ◽  
Vol 6 (17) ◽  
pp. 4641-4648 ◽  
Author(s):  
S. X. Lim ◽  
Y. Z. Lee ◽  
N. Gao ◽  
J. Lu ◽  
Q. Xu ◽  
...  
Keyword(s):  
Thin Film ◽  
Silver Nanoparticles ◽  
Graphene Oxide ◽  
Oxide Film ◽  
Silver Nanoclusters ◽  
Site Selective ◽  
Selective Formation

Laser initiated site selective formation of dynamic tri-colour blinking silver nanoparticles on a transparent, flexible GO thin film.

scholarly journals Site-selective Formation of Polymer Ultrathin Films using the Ink-jet Method onto Patterned Fluoroalkylsilane Monolayer Substrate

Hyomen Kagaku ◽  
2006 ◽  
Vol 27 (2) ◽  
pp. 108-115 ◽  
Author(s):  
Masamichi MORITA ◽  
Shigekazu YASUTAKE ◽  
Hirotaka ISHIZUKA ◽  
Jun FUKAI ◽  
Atsushi TAKAHARA
Keyword(s):  
Ultrathin Films ◽  
Ink Jet ◽  
Site Selective ◽  
Selective Formation

Building Addressable Libraries: Site-Selective Formation of anN-Acyliminium Ion Intermediate

2008 ◽  
Vol 10 (12) ◽  
pp. 2501-2504 ◽  
Author(s):  
David Kesselring ◽  
Karl Maurer ◽  
Kevin D. Moeller
Keyword(s):  
Site Selective ◽  
Selective Formation

Corrigendum to “Site-selective formation of N-arylmethylimidazoles and C-arylimines in the reaction of 4,5-diamino-2,1,3-benzothiadiazole with aromatic aldehydes”

Tetrahedron ◽  
2004 ◽  
Vol 60 (44) ◽  
pp. 10117
Author(s):  
Akihito Saitoh ◽  
Keiji Okinaka ◽  
Koichi Suzuki ◽  
Akihiro Seno ◽  
Maki Kasahara ◽  
...  
Keyword(s):  
Aromatic Aldehydes ◽  
Site Selective ◽  
Selective Formation

scholarly journals Modular synthesis of oligoacetylacetones via site-selective silylation of acetylacetone derivatives

2020 ◽  
Vol 18 (17) ◽  
pp. 3297-3302 ◽  
Author(s):  
Parantap Sarkar ◽  
Yuya Inaba ◽  
Hayato Shirakura ◽  
Tomoki Yoneda ◽  
Yasuhide Inokuma
Keyword(s):  
Solid State ◽  
X Ray ◽  
Silyl Ethers ◽  
X Ray Crystallography ◽  
Modular Synthesis ◽  
Conformational Preferences ◽  
Enol Silyl Ethers ◽  
Site Selective ◽  
Selective Formation

Aliphatic oligoketones with tailored carbonyl and substituent sequences were modularly synthesized utilizing site-selective formation of enol silyl ethers. Their unique conformational preferences in solid-state were revealed by X-ray crystallography.

Synthesis of functionalised fluorinated pyridine derivatives by site-selective Suzuki-Miyaura cross-coupling reactions of halogenated pyridines

2017 ◽  
Vol 72 (4) ◽  
pp. 263-279 ◽  
Author(s):  
Muhammad Sharif ◽  
Khurram Shoaib ◽  
Shahzad Ahmed ◽  
Sebastian Reimann ◽  
Jamshed Iqbal ◽  
...  
Keyword(s):  
Cross Coupling ◽  
Phosphine Ligands ◽  
Coupling Reactions ◽  
Pyridine Derivatives ◽  
One Pot ◽  
Arylboronic Acids ◽  
Cross Coupling Reactions ◽  
The One ◽  
Site Selective ◽  
Selective Formation

AbstractThe Suzuki-Miyaura reaction of 2,6-dichloro-3-(trifluoromethyl)pyridine with 1 equiv of arylboronic acids resulted in site-selective formation of 2-aryl-6-chloro-3-(trifluoromethyl)pyridine. Due to electronic reasons, the reaction takes place at the sterically more hindered position. The selectivity was rationalised by DFT calculations. The one-pot reaction with two different arylboronic acids afforded 2,6-diaryl-3-(trifluoromethyl)pyridine containing two different aryl substituents. The reactions proceeded smoothly in the absence of phosphine ligands. In addition, Suzuki-Miyaura reactions of 2,6-dichloro-4-(trifluoromethyl)pyridine with one or two equivalents of arylboronic acids were carried out.

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