Highly Enantioselective Synthesis of 1,2-Amino Alcohol Derivatives via Proline-Catalyzed Mannich Reaction

Synlett ◽  
2003 ◽  
pp. 1903-1905 ◽  
Author(s):  
Benjamin List ◽  
Peter Pojarliev ◽  
William T. Biller ◽  
Harry J. Martin
Keyword(s):  
Mannich Reaction ◽  
Amino Alcohol ◽  
Enantioselective Synthesis

Highly Enantioselective Synthesis of 1,2-Amino Alcohol Derivatives via Proline-Catalyzed Mannich Reaction.

ChemInform ◽  
2004 ◽  
Vol 35 (6) ◽  
Author(s):  
Peter Pojarliev ◽  
William T. Biller ◽  
Harry J. Martin ◽  
Benjamin List
Keyword(s):  
Mannich Reaction ◽  
Amino Alcohol ◽  
Enantioselective Synthesis

scholarly journals Highly Enantioselective Synthesis of Fluorinated γ-Amino Alcohols Through Proline-Catalyzed Cross-Mannich Reaction.

ChemInform ◽  
2005 ◽  
Vol 36 (48) ◽  
Author(s):  
Santos Fustero ◽  
Diego Jimenez ◽  
Juan F. Sanz-Cervera ◽  
Maria Sanchez-Rosello ◽  
Elisabet Esteban ◽  
...  
Keyword(s):  
Mannich Reaction ◽  
Amino Alcohols ◽  
Enantioselective Synthesis

Enantioselective synthesis of α,α-difluoro-β-lactams using amino alcohol ligands

2014 ◽  
Vol 12 (33) ◽  
pp. 6484-6489 ◽  
Author(s):  
Atsushi Tarui ◽  
Takeshi Ikebata ◽  
Kazuyuki Sato ◽  
Masaaki Omote ◽  
Akira Ando
Keyword(s):  
Amino Alcohol ◽  
Enantioselective Synthesis ◽  
Reformatsky Reaction

A practical and highly enantioselective Reformatsky reaction of ethyl bromodifluoroacetate with imines using a cheap and commercially available amino alcohol ligand is described.

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