Absolute Asymmetric Synthesis of Tertiary α-Amino Acids

2012 ◽  
Vol 124 (20) ◽  
pp. 5065-5068 ◽  
Author(s):  
Thi Thoa Mai ◽  
Mathieu Branca ◽  
Didier Gori ◽  
Régis Guillot ◽  
Cyrille Kouklovsky ◽  
...  
ChemInform ◽  
2012 ◽  
Vol 43 (40) ◽  
pp. no-no
Author(s):  
Thi Thoa Mai ◽  
Mathieu Branca ◽  
Didier Gori ◽  
Regis Guillot ◽  
Cyrille Kouklovsky ◽  
...  

2012 ◽  
Vol 51 (20) ◽  
pp. 4981-4984 ◽  
Author(s):  
Thi Thoa Mai ◽  
Mathieu Branca ◽  
Didier Gori ◽  
Régis Guillot ◽  
Cyrille Kouklovsky ◽  
...  

2018 ◽  
Vol 54 (77) ◽  
pp. 10832-10834 ◽  
Author(s):  
Iaroslav Baglai ◽  
Michel Leeman ◽  
Klaus Wurst ◽  
Bernard Kaptein ◽  
Richard M. Kellogg ◽  
...  

We introduce a methodology based on a combination of the classical Strecker reaction, simple condensation and Viedma ripening, which allows absolute asymmetric synthesis of highly sterically hindered α-amino acids. As proof-of-principle, enantiomerically pure unnatural α-amino acids tert-leucine and α-(1-adamantyl)glycine have been obtained.


1997 ◽  
Vol 38 (29) ◽  
pp. 5135-5138 ◽  
Author(s):  
Yinglin Han ◽  
Subo Liao ◽  
Wei Qiu ◽  
Chaozhong Cai ◽  
Victor J. Hruby

ChemInform ◽  
2010 ◽  
Vol 24 (46) ◽  
pp. no-no
Author(s):  
U. GROTH ◽  
T. HUHN ◽  
B. PORSCH ◽  
C. SCHMECK ◽  
U. SCHOELLKOPF

ChemInform ◽  
2013 ◽  
Vol 44 (24) ◽  
pp. no-no
Author(s):  
Wahid Bux Jatoi ◽  
Agnes Desiront ◽  
Aurelie Job ◽  
Yves Troin ◽  
Jean-Louis Canet

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