ChemInform Abstract: Stereoselective Synthesis of Densely Substituted Tetrahydroquinolines by a Conjugate Addition Nitro-Mannich Reaction with Carbon Nucleophiles.

ChemInform ◽  
2016 ◽  
Vol 47 (23) ◽  
Author(s):  
James C. Anderson ◽  
Christopher D. Rundell
ChemInform ◽  
2015 ◽  
Vol 46 (20) ◽  
pp. no-no
Author(s):  
James C. Anderson ◽  
Ian B. Campbell ◽  
Sebastien Campos ◽  
Jonathan Shannon ◽  
Derek A. Tocher

2015 ◽  
Vol 13 (1) ◽  
pp. 170-177 ◽  
Author(s):  
James C. Anderson ◽  
Ian B. Campbell ◽  
Sebastien Campos ◽  
Jonathan Shannon ◽  
Derek A. Tocher

The sequential use of the conjugate addition nitro-Mannich reaction, nitro reduction and then Pd-catalyzed intramolecular cyclisation allows the concise, stereodivergent synthesis of complex indolines.


2016 ◽  
Vol 14 (35) ◽  
pp. 8270-8277 ◽  
Author(s):  
James C. Anderson ◽  
Ian B. Campbell ◽  
Sebastien Campos ◽  
Iain H. Reid ◽  
Christopher D. Rundell ◽  
...  

A reductive conjugate addition nitro-Mannich reaction controls diastereoselectivity in a rapid entry to a diverse array of 1,2,3,4-tetrahydroquinoxalines in high yield.


2017 ◽  
Vol 19 (17) ◽  
pp. 4460-4463 ◽  
Author(s):  
Christian A. Malapit ◽  
Irungu K. Luvaga ◽  
Donald R. Caldwell ◽  
Nicholas K. Schipper ◽  
Amy R. Howell

2013 ◽  
Vol 15 (23) ◽  
pp. 6111-6112 ◽  
Author(s):  
Benny Meng Kiat Tong ◽  
Hui Chen ◽  
Sin Yee Chong ◽  
Yi Li Heng ◽  
Shunsuke Chiba

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