X=Y-ZH compounds as potential 1,3-Dipoles. Part 281,2 the iminium ion route to azomethine ylides. background and reaction of amines with bifunctional ketones.

Tetrahedron

Volumn 46, Issue 18, 1990, Pages 6433-6448

  Ardill, Harriet ^a   Dorrity, M J R ^a   Grigg, Ronald ^b   Leon Ling, Mooi Sin ^a   Malone, J F ^a   Sridharan, Visuvanathar ^b   Thianpatanagul , Sunit ^c  

^a QUEEN'S UNIVERSITY BELFAST   (United Kingdom)

^b UNIVERSITY OF LEEDS   (United Kingdom)

^c SILPAKORN UNIVERSITY   (Thailand)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 0001597029     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4020(01)96013-2     Document Type: Article

References (33)

1. Iminium ion route to azomethine yields from primary and secondary amines
2. X?Y?ZH systems as potential 1,3-dipoles. Part 3. Isoxazolidines from the 1:1 cycloaddition of oximes with dipolarophiles
3. X?Y?ZH systems as potential 1,3-dipoles. Part 11. Stereochemistry of 1,3-dipoles generated by the decarboxylative route to azomethine ylides
4. X?Y?ZH systems as potential 1,3-dipoles. Part 12. Mechanism of formation of azomethine ylides via the decarboxylative route from ?-amino acids
5. Cycloaddition reactions of oximes; powerful new carbon?carbon bond forming methodology
6. Tandem intramolecular Michael addition and 1,3-dipolar cycloaddition reactions of oximes; versatile new carbon?carbon bond forming methodology
7. A dehydrogenation route to azomethine ylides and isoindoles
8. Die Dienol-Benzol-Umlagerung von Allyldienolen: aromatische [1,2]-, [3,3]- und [3,4]-sigmatropische Umlagerungen
9. The “tert-amino effect” in heterocyclic chemistry: Synthesis of tetra- and pentacyclic compounds
10. 44. Degradation of ?-amino-acids to aldehydes and ketones by interaction with carbonyl compounds
11. X?Y?ZH systems as potential 1,3-dipoles. Part 10. The decarboxylative route to azomethine ylides. Background and relevance to pyridoxal decarboxylases
12. X=Y-ZH systems as potential 1,3-dipoles. The stereochemistry and regiochemistry of cycloaddition reactions of imines of α-amino-acid esters.
13. Aza-2-di�nes-1,3. 2. Synth�se et structure d'un ylure d'azom�thine stable
14. X?Y?ZH systems as potential 1,3-dipoles. Part 1. Background and scope
15. 691. The structure of isatin blue