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Angewandte Chemie (International ed.), ISSN 1433-7851, 11/2013, Volume 52, Issue 48, pp. 12641 - 12645
The more dipoles, the merrier: An asymmetric [3+3] cycloaddition of azomethine ylides derived from imines 1 with azomethine imines 2 in the presence of a chiral ferrocenylphosphine... 
azomethine ylides | copper | asymmetric catalysis | azomethine imines | [3+3] cycloaddition | Enantiomers | Copper | Schiff bases | Cycloaddition | Dipoles | Asymmetry | Imines | Catalysts | Aldehydes
Journal Article
Chemical communications (Cambridge, England), ISSN 1364-548X, 2014, Volume 50, Issue 83, pp. 12434 - 12446
The scope of the catalytic asymmetric 1,3-dipolar cycloaddition of azomethine ylides has been greatly expanded by the incorporation of novel types of dipolarophiles and dipole precursors... 
Physical Sciences | Chemistry | Chemistry, Multidisciplinary | Science & Technology | Cycloaddition | Catalysis | Asymmetry | Catalysts
Journal Article
Chemistry : a European journal, ISSN 0947-6539, 07/2015, Volume 21, Issue 29, pp. 10457 - 10465
...‐dipolar cycloaddition of azomethine ylides to α‐phthalimidoacrylates. Reactions catalyzed by copper in combination with ligand 7‐Cl... 
density functional calculations | ligands | copper | asymmetric synthesis | cycloaddition | Ligands | Cycloaddition | Density functional calculations | Asymmetric synthesis | Copper
Journal Article
European journal of organic chemistry, ISSN 1434-193X, 07/2015, Volume 2015, Issue 21, pp. 4689 - 4698
Azomethine ylides, generated from imine‐derived O‐cinnamyl or O‐crotonyl salicylaldeyde and α... 
Transition states | Cycloaddition | Kinetics | Azomethine ylides | Reaction mechanisms | Nitrogen | Schiff bases | Analysis
Journal Article
Chemistry : a European journal, ISSN 0947-6539, 08/2016, Volume 22, Issue 33, pp. 11473 - 11473
A catalytic amount of nBuLi is enough for launching a catalytic cycle, in which a nitrone ylide reacts with an aldehyde through a two... 
azomethine ylides | density functional calculations | lithium | oxazolines | nitrones | Cycloaddition | Catalysts | Lithium | Visual stimuli | Forming | Launching | Chemical synthesis
Journal Article
Molecules (Basel, Switzerland), ISSN 1420-3049, 02/2019, Volume 24, Issue 3, p. 601
Journal Article
Pure and applied chemistry, ISSN 0033-4545, 04/2019, Volume 91, Issue 4, pp. 575 - 596
Journal Article
Angewandte Chemie (International ed.), ISSN 1433-7851, 11/2012, Volume 51, Issue 47, pp. 11819 - 11823
Put it on a ring: A rhodium(III) complex can catalyze the oxidative coupling of azomethine imines with olefins, leading to the synthesis of... 
C‐H activation | oxidative coupling | azomethines | olefination | rhodium | C-H activation | Pyridines | Joining | Synthesis | Imines | Aldehydes | Olefins
Journal Article
Synlett, ISSN 0936-5214, 05/2017, Volume 28, Issue 8, pp. 999 - 1003
...] cycloaddition of azomethine ylides with electronic-deficient alkenes with or without Et 3 N. Under optimal conditions, highly functionalized endo -4-pyrrolidines were obtained with modest to high yields (up to 99% yield... 
letter | amidophosphane | l-tert-leucine | silver(I) | azomethine ylide | [3+2] cycloaddition
Journal Article
Angewandte Chemie (International ed.), ISSN 1433-7851, 05/2016, Volume 55, Issue 21, pp. 6324 - 6328
Reported herein is an asymmetric [3+2] cycloaddition reaction of azomethine ylides with β‐trifluoromethyl β,β... 
azomethine ylides | copper | cycloaddition | heterocycles | P,O ligand | P,O ligand | Cycloaddition | Enantiomers | Copper | Functional groups | Substrates
Journal Article
Chemistry of Heterocyclic Compounds, ISSN 0009-3122, 12/2018, Volume 54, Issue 12, pp. 1084 - 1107
In this review, we consider 1,3-dipolar cycloaddition reactions between azomethine ylides and alkynes, resulting in the formation of pyrroles, as well as their hydrogenated and fused analogs... 
azomethine ylides | Chemistry | Pharmacy | alkynes | pyrroles | Organic Chemistry | fused pyrroles | 1,3-dipolar cycloaddition | Physical Sciences | Chemistry, Organic | Science & Technology | Schiff bases | Cycloaddition | Pyrroles | Alkynes
Journal Article