Enantioselective 2-Alkylation of 3-Substituted Indoles with Dual Chiral Lewis Acid/Hydrogen-Bond-Mediated Catalyst

2016 ◽  
Vol 19 (1) ◽  
pp. 222-225 ◽  
Author(s):  
Zijun Zhou ◽  
Yanjun Li ◽  
Lei Gong ◽  
Eric Meggers
1980 ◽  
Vol 45 (2) ◽  
pp. 335-338 ◽  
Author(s):  
Adéla Kotočová ◽  
Ulrich Mayer

The solvation effect of a number of nonaqueous polar solvents was studied on the oxidation-reduction properties of the [Co(en)3]3+-[Co(en)3]2+ system. Interactions of these ions with the solvent molecules are discussed in terms of their coordination, which is accompanied by a specific interaction of the Lewis acid-base type, namely formation of a hydrogen bond between the interacting particles. This is the main controlling factor of the redox properties of the studied system.


Tetrahedron ◽  
2012 ◽  
Vol 68 (6) ◽  
pp. 1774-1781 ◽  
Author(s):  
Chigusa Seki ◽  
Masafumi Hirama ◽  
N.D.M. Romauli Hutabarat ◽  
Junko Takada ◽  
Chonticha Suttibut ◽  
...  

2004 ◽  
Vol 126 (17) ◽  
pp. 5366-5367 ◽  
Author(s):  
Mukund P. Sibi ◽  
Kennosuke Itoh ◽  
Craig P. Jasperse

ChemInform ◽  
2006 ◽  
Vol 37 (12) ◽  
Author(s):  
Shih-Yuan Liu ◽  
Ivory D. Hills ◽  
Gregory C. Fu

2016 ◽  
Vol 7 (4) ◽  
pp. 2717-2721 ◽  
Author(s):  
Jing Guo ◽  
Yangbin Liu ◽  
Xiangqiang Li ◽  
Xiaohua Liu ◽  
Lili Lin ◽  
...  

A chiral Lewis acid-promoted cyclopropanation using a phenyliodonium ylide as the carbene precursor was developed. An EPR spectroscopy study supported a stepwise biradical mechanism.


1995 ◽  
Vol 117 (3) ◽  
pp. 1165-1166 ◽  
Author(s):  
Keiji Maruoka ◽  
Susumu Saito ◽  
Hisashi Yamamoto

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