Catalytic CSe Bond Formation under Very Mild Conditions for the Two-Step, One-Pot Synthesis of Aryl Selenoacetates

2012 ◽  
Vol 354 (14-15) ◽  
pp. 2653-2658 ◽  
Author(s):  
Konstantin Grenader ◽  
Björn Schüpbach ◽  
Annabell Peters ◽  
Oliver Kümmel ◽  
Oliver Halter ◽  
...  
ChemInform ◽  
2013 ◽  
Vol 44 (11) ◽  
pp. no-no
Author(s):  
Konstantin Grenader ◽  
Bjoern Schuepbach ◽  
Annabell Peters ◽  
Oliver Kuemmel ◽  
Oliver Halter ◽  
...  

2017 ◽  
Vol 28 (6) ◽  
pp. e21408 ◽  
Author(s):  
Samia Guezane-Lakoud ◽  
Martial Toffano ◽  
Louisa Aribi-Zouioueche

2007 ◽  
Vol 48 (10) ◽  
pp. 1809-1811 ◽  
Author(s):  
Christopher A. Simoneau ◽  
Alexis M. Strohl ◽  
Bruce Ganem

ChemInform ◽  
2015 ◽  
Vol 46 (13) ◽  
pp. no-no
Author(s):  
Trimurtulu Kotipalli ◽  
Donala Janreddy ◽  
Veerababurao Kavala ◽  
Chun-Wei Kuo ◽  
Ting-Shen Kuo ◽  
...  

Synthesis ◽  
2019 ◽  
Vol 51 (22) ◽  
pp. 4215-4230 ◽  
Author(s):  
Adesh Kumar Singh ◽  
Rapelly Venkatesh ◽  
Jeyakumar Kandasamy

The palladium-catalyzed one-pot synthesis of 2,3-deoxy-3-keto aryl C-glycosides is achieved from glycals and anilines in the presence of tert-butyl nitrite and aqueous HBF4 under mild conditions. This one-pot method stereospecifically provides α- and β-aryl glycosides (≥19:1 by NMR) in good yields at room temperature. The configuration at the C-3 position in the glycal determines the anomeric selectivity (i.e., α or β) of the desired products.


2020 ◽  
Vol 39 (5-6) ◽  
pp. 267-287
Author(s):  
Shuang Hao ◽  
Shuai Lin ◽  
Xin Wang ◽  
Ran An ◽  
Mengbi Guo ◽  
...  

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