scholarly journals Asymmetric Reduction of Chiral Acetophenone Oxime Ethers to Optically Active Primary Amines

1986 ◽  
Vol 15 (7) ◽  
pp. 1133-1136 ◽  
Author(s):  
Shinichi Itsuno ◽  
Kazuo Tanaka ◽  
Koichi Ito
Keyword(s):  
Asymmetric Reduction ◽  
Optically Active ◽  
Primary Amines ◽  
Acetophenone Oxime

scholarly journals Enantioselective Transfer Aminoallylation: Synthesis of Optically Active Homoallylic Primary Amines.

ChemInform ◽  
2007 ◽  
Vol 38 (1) ◽  
Author(s):  
Masaharu Sugiura ◽  
Chieko Mori ◽  
Shu Kobayashi
Keyword(s):  
Optically Active ◽  
Primary Amines

scholarly journals Direct asymmetric reduction of levulinic acid to gamma-valerolactone: synthesis of a chiral platform molecule

2015 ◽  
Vol 17 (12) ◽  
pp. 5189-5195 ◽  
Author(s):  
József M. Tukacs ◽  
Bálint Fridrich ◽  
Gábor Dibó ◽  
Edit Székely ◽  
László T. Mika
Keyword(s):  
Levulinic Acid ◽  
Asymmetric Reduction ◽  
Optically Active

Biomass-originated levulinic acid was directly converted to optically active (S)-gamma-valerolactone, a proposed biomass-based chiral platform molecule.

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