Skip to search formSkip to main contentSkip to account menu

Imines

Known as: Imines [Chemical/Ingredient], imine 
National Institutes of Health

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Review
2010
Review
2010
This Review deals with the asymmetric hydrogenation and asymmetric transfer hydrogenation of imines and some nitrogen‐containing… 
Highly Cited
2009
Highly Cited
2009
Two birds with one auric stone: The title system acts as a highly efficient heterogeneous catalyst for the one-pot tandem… 
Review
2009
Review
2009
Since Ellman's seminal works, over the past ten years tert-butanesulfinimines have proved to be useful chiral amino intermediates… 
Highly Cited
2008
Highly Cited
2008
The Lewis acid B(C(6)F(5))(3) has been found to be an efficient catalyst for the direct hydrogenation of imines and the reductive… 
Highly Cited
2008
Highly Cited
2008
When combined with a chiral phosphate counteranion, a chiral diamine-ligated Ir(III) catalyst displayed excellent… 
Highly Cited
2004
Highly Cited
2004
The first highly enantioselective catalytic reaction involving aromatic C-H bond activation is communicated. Enantioselective… 
Highly Cited
2002
Highly Cited
2002
Dendrimers are highly branched organic macromolecules with successive layers or ‘generations’ of branch units surrounding a… 
Highly Cited
2000
Highly Cited
2000
A broad range of benzaldimines and ketimines can be hydrosilated efficiently, employing B(C(6)F(5))(3) as a catalyst in… 
Highly Cited
1993
Highly Cited
1993
Theoretical Description of the Bonding in Ylides Introduction to Phosphonium Ylides Preparation of Phosphonium Ylides Reactions…