Diastereoselective desymmetrization of diarylphosphinous acid-borane amides under Birch reduction

2015 ◽  
Vol 13 (21) ◽  
pp. 6082-6102 ◽  
Author(s):  
Marek Stankevič
Keyword(s):  
Birch Reduction ◽  
Amido Group

Birch reduction of symmetrical diarylphosphinous acid-borane amides possessing a chiral amido group, proceeds with diastereoselectivity up to 72%.

Silyl substituted furans in the stereoselective Birch reduction

2001 ◽  
Vol 42 (34) ◽  
pp. 5841-5844 ◽  
Author(s):  
Timothy J Donohoe ◽  
Jean-Baptiste Guillermin ◽  
Andrew A Calabrese ◽  
Daryl S Walter
Keyword(s):  
Birch Reduction ◽  
Substituted Furans

Syntheses and structures of highly hindered N-functionalised alkyl and amido group 12 complexes MR2 (M=Zn, Cd, and Hg), [MRCl]2 (M=Zn and Hg)

2004 ◽  
Vol 689 (11) ◽  
pp. 1991-1999 ◽  
Author(s):  
Tania R van den Ancker ◽  
Lutz M Engelhardt ◽  
Mark J Henderson ◽  
Geraldine E Jacobsen ◽  
Colin L Raston ◽  
...  
Keyword(s):  
Amido Group ◽  
Group 12

ChemInform Abstract: A Cooperative Participation of the Amido Group in the Organocatalytic Construction of All-Carbon Quaternary Stereocenters by Michael Addition with β-Ketoamides.

ChemInform ◽  
2011 ◽  
Vol 42 (43) ◽  
pp. no-no
Author(s):  
Maria del Mar Sanchez Duque ◽  
Olivier Basle ◽  
Nicolas Isambert ◽  
Anouk Gaudel-Siri ◽  
Yves Genisson ◽  
...  
Keyword(s):  
Michael Addition ◽  
Amido Group ◽  
Quaternary Stereocenters

The origin of the Birch reduction

1975 ◽  
Vol 52 (7) ◽  
pp. 458 ◽  
Author(s):  
A. J. Birch
Keyword(s):  
Birch Reduction

Birch reduction of biphenylene. Formation of 4,5-benzobicyclo[4.2.0]octa-2,4-diene

1972 ◽  
Vol 37 (21) ◽  
pp. 3345-3346 ◽  
Author(s):  
Charles A. Matuszak ◽  
Luther. Dickson
Keyword(s):  
Birch Reduction
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