نتایج جستجو برای: bf3 detector

تعداد نتایج: 59041  

2015
Davide Bello David O'Hagan

A new method for the preparation of α-fluorovinyl thioethers is reported which involves the hydrofluorination of alkynyl sulfides with 3HF·Et3N, a process that requires Lewis acid activation using BF3·Et2O and TiF4. The method gives access to a range of α-fluorovinyl thioethers, some in high stereoselectivity with the Z-isomer predominating over the E-isomer. The α-fluorovinyl thioether motif h...

2010
SMITA SHARMA M. C. SHARMA Smita Sharma M. C. Sharma

Synthesis of Some Benzimidazole derivatives 4'-(5, 6-substitued-2-trifluoromethylbenzoimidazol-1-ylmethyl)-biphenyl-2-carboxylic acid were synthesized by condensation of various steps with different o-Phenylenediamine was condensed with in propylene glycol was added trifluoroacetic acid in the presence of BF3•OEt2 as catalysis. Elemental analysis, IR, 1HNMR and mass spectral data confirmed the ...

Journal: :The Journal of the Society of Chemical Industry, Japan 1968

2014
Kate D. Otley Jonathan A. Ellman

We report here a new, atom economical annulation to 2,1-benzisoxazole scaffolds via the BF3·Et2O-catalyzed reaction of glyoxylate esters and nitrosoarenes. The developed method represents a convergent route to this compound class from previously unexplored inputs and provides a range of 2,1-benzisoxazoles in moderate to high yields under convenient conditions. Along with exploration of substrat...

Journal: :Organic letters 2014
Zhengxu S Han Yibo Xu Daniel R Fandrick Sonia Rodriguez Zhibin Li Bo Qu Nina C Gonnella Sanjit Sanyal Jonathan T Reeves Shengli Ma Nelu Grinberg Nizar Haddad Dhileep Krishnamurthy Jinhua J Song Nathan K Yee Waldemar Pfrengle Markus Ostermeier Jürgen Schnaubelt Zeno Leuter Sonja Steigmiller Jürgen Däubler Emanuel Stehle Lukas Neumann Thomas Trieselmann Patrick Tielmann Annette Buba Rainer Hamm Gunter Koch Svenja Renner Juan R Dehli Florian Schmelcher Christian Stange Jürgen Mack Rainer Soyka Chris H Senanayake

An efficient enantioselective synthesis of the chiral polycyclic cholesteryl ester transfer protein (CETP) inhibitor 1 has been developed. The synthesis was rendered practical for large scale via the development of a modified Hantzsch-type reaction to prepare the sterically hindered pyridine ring, enantioselective hydrogenation of hindered ketone 6 utilizing novel BIBOP-amino-pyridine derived R...

Journal: :Yakugaku zasshi : Journal of the Pharmaceutical Society of Japan 2003
Hideto Miyabe

This review summarizes the new carbon-carbon bond construction methods based on the radical reaction of imine derivatives. The intermolecular carbon radical addition to oxime ethers proceeded smoothly in the presence of BF3.OEt2. A high degree of stereocontrol in the reaction of oxime ethers was achieved to give amino acid derivatives with excellent diastereoselectivities. The radical reaction ...

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