imine allylation
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Neighboring phenolic group-activated gem-difluoroallylboration of imines for the catalyst-free synthesis of gem-difluorohomoallylamines

2018 ◽  
Vol 16 (18) ◽  
pp. 3367-3371 ◽  
Author(s):  
Xing Yang ◽  
Feng Zhang ◽  
Yang Zhou ◽  
Yi-Yong Huang
Keyword(s):  
Protecting Group ◽  
Catalyst Free ◽  
Wide Range ◽  
Phenolic Group ◽  
Imine Allylation

An unprecedented imine allylation with pinacol gem-difluoroallylborates for the synthesis of a wide range of racemic gem-difluorohomoallylamine derivatives under catalyst-free conditions was enabled by a neighboring phenolic group in an N-protecting group.

Allylsilane–Vinylarene Cross-Metathesis Enables a Powerful Approach to Enantioselective Imine Allylation

2008 ◽  
Vol 120 (16) ◽  
pp. 3079-3081 ◽  
Author(s):  
John D. Huber ◽  
Nicholas R. Perl ◽  
James L. Leighton
Keyword(s):  
Cross Metathesis ◽  
Powerful Approach ◽  
Imine Allylation

Allylsilane–Vinylarene Cross-Metathesis Enables a Powerful Approach to Enantioselective Imine Allylation

2008 ◽  
Vol 47 (16) ◽  
pp. 3037-3039 ◽  
Author(s):  
John D. Huber ◽  
Nicholas R. Perl ◽  
James L. Leighton
Keyword(s):  
Cross Metathesis ◽  
Powerful Approach ◽  
Imine Allylation

scholarly journals Readily Accessible, Modular, and Tuneable BINOL 3,3′-Perfluoroalkylsulfones: Highly Efficient Catalysts for Enantioselective In-Mediated Imine Allylation.

ChemInform ◽  
2007 ◽  
Vol 38 (35) ◽  
Author(s):  
Robert Kargbo ◽  
Yoko Takahashi ◽  
Santosh Bhor ◽  
Gregory R. Cook ◽  
Guy C. Lloyd-Jones ◽  
...  
Keyword(s):  
Highly Efficient ◽  
Imine Allylation

Readily Accessible, Modular, and Tuneable BINOL 3,3‘-Perfluoroalkylsulfones:  Highly Efficient Catalysts for Enantioselective In-Mediated Imine Allylation

2007 ◽  
Vol 129 (13) ◽  
pp. 3846-3847 ◽  
Author(s):  
Robert Kargbo ◽  
Yoko Takahashi ◽  
Santosh Bhor ◽  
Gregory R. Cook ◽  
Guy C. Lloyd-Jones ◽  
...  
Keyword(s):  
Highly Efficient ◽  
Imine Allylation
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