scholarly journals Biaryl synthesis with control of axial chirality

2006 ◽  
Vol 4 (17) ◽  
pp. 3197 ◽  
Author(s):  
Timothy W. Wallace
ChemInform ◽  
2007 ◽  
Vol 38 (1) ◽  
Author(s):  
Timothy W. Wallace

1996 ◽  
Vol 61 (7) ◽  
pp. 1018-1026 ◽  
Author(s):  
Richard Kubík ◽  
Stanislav Böhm ◽  
Josef Kuthan

Borohydride reduction of titled ketones 1a-1g gave diastereoisomeric mixtures of (Z)-1,3-diphenyl-3-(2-phenylimidazo[1,2-a]pyridin-3-yl)prop-2-en-1-ols 2a-2g and 3a-3g in which the former ones prevailed. Only individual racemic products were obtained after borohydride reduction of (E)-1,3-diphenyl-3-(2-phenylimidazo[1,2-a]pyridin-3-yl)-prop-2-en-1-one 4 to corresponding 1-hydroxy derivative 5 and by conversion of (Z)-1-oxo derivative 1a to 1,3-diphenyl-3-(2-phenylimidazo[1,2-a]pyridin-3-yl)propan-1-one (6) with sodium hydrogenselenide. Diastereoselectivity of the borohydride reduction is discussed using the PM3 calculations of the molecules 1a, 2a, 2b, 3a, 3b, 4, 5, and 6.


2021 ◽  
Vol 60 (17) ◽  
pp. 9362-9367
Author(s):  
Tingting Li ◽  
Chengli Mou ◽  
Puying Qi ◽  
Xiaolin Peng ◽  
Shichun Jiang ◽  
...  
Keyword(s):  

2021 ◽  
Author(s):  
Qianghui Zhou ◽  
Chenggui Wu ◽  
Yong Shang ◽  
Chang Liu ◽  
Ze-Shui Liu ◽  
...  
Keyword(s):  

ChemInform ◽  
2007 ◽  
Vol 38 (16) ◽  
Author(s):  
Hidenori Mizuno ◽  
Hidehiro Sakurai ◽  
Toru Amaya ◽  
Toshikazu Hirao
Keyword(s):  

2018 ◽  
Vol 130 (24) ◽  
pp. 7254-7257 ◽  
Author(s):  
Achim Link ◽  
Christof Sparr
Keyword(s):  

1998 ◽  
Vol 39 (19) ◽  
pp. 2945-2946 ◽  
Author(s):  
Marko M Schmitt ◽  
Ellen Schüler ◽  
Myriam Braun ◽  
Dietmar Häring ◽  
Peter Schreier

Synthesis ◽  
2021 ◽  
Author(s):  
Jonas Felix Goebel ◽  
Zhongyi Zeng ◽  
Lukas Goossen

The use of electricity as an inexpensive and waste-free oxidant opens up new opportunities for the development of sustainable C–H functionalization reactions. Herein we summarize recent advances in the synthesis of biaryls through electrooxidative processes involving transition metal catalyzed ortho-directed C−H activation. A particular focus is set on electrooxidative C−H/C−M couplings and dehydrogenative couplings.


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