ChemInform Abstract: Diastereoselective Synthesis of Substituted Tetrahydroquinoline-4-carboxylic Esters by a Tandem Reduction-Reductive Amination Reaction.

ChemInform ◽  
2010 ◽  
Vol 32 (36) ◽  
pp. no-no
Author(s):  
Richard A. Bunce ◽  
Derrick M. Herron ◽  
Lara B. Johnson ◽  
Sharadsrikar V. Kotturi
Keyword(s):  
Reductive Amination ◽  
Diastereoselective Synthesis ◽  
Amination Reaction ◽  
Carboxylic Esters

Diastereoselective synthesis of linear-fused tricyclic nitrogen heterocycles by a tandem reduction-reductive amination reaction

2003 ◽  
Vol 40 (1) ◽  
pp. 101-106 ◽  
Author(s):  
Richard A. Bunce ◽  
Derrick M. Herron ◽  
Jason R. Lewis ◽  
Sharadsrikar V. Kotturi ◽  
Elizabeth M. Holt
Keyword(s):  
Reductive Amination ◽  
Nitrogen Heterocycles ◽  
Diastereoselective Synthesis ◽  
Amination Reaction

Diastereoselective Synthesis of Linear-Fused Tricyclic Nitrogen Heterocycles by a Tandem Reduction-Reductive Amination Reaction.

ChemInform ◽  
2003 ◽  
Vol 34 (26) ◽  
Author(s):  
Richard A. Bunce ◽  
Derrick M. Herron ◽  
Jason R. Lewis ◽  
Sharadsrikar V. Kotturi ◽  
Elizabeth M. Holt
Keyword(s):  
Reductive Amination ◽  
Nitrogen Heterocycles ◽  
Diastereoselective Synthesis ◽  
Amination Reaction

(±)-2,3-dialkyl-1,2,3,4-tetrahydroquinoline-3-carboxylic esters by a tandem reduction-reductive amination reaction

2007 ◽  
Vol 44 (5) ◽  
pp. 1051-1057 ◽  
Author(s):  
Richard A. Bunce ◽  
James E. Schammerhorn ◽  
LeGrande M. Slaughter
Keyword(s):  
Reductive Amination ◽  
Amination Reaction ◽  
Carboxylic Esters

scholarly journals Computational investigation of the control of the thermodynamics and microkinetics of the reductive amination reaction by solvent coordination and a co-catalyst

RSC Advances ◽  
2018 ◽  
Vol 8 (64) ◽  
pp. 36662-36674 ◽  
Author(s):  
Esra Boz ◽  
Nurcan Ş. Tüzün ◽  
Matthias Stein
Keyword(s):  
Tertiary Amine ◽  
Reductive Amination ◽  
Computational Investigation ◽  
Reaction Parameters ◽  
Co Catalyst ◽  
Amination Reaction ◽  
Green Production

Green production of tertiary amine from sustainable sources can be controlled by appropriate choice of reaction parameters identified by computational means.

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