Desymmetrization of dichloroazaheterocycles

Tetrahedron

Volumn 55, Issue 52, 1999, Pages 15067-15070

  Goodman, Allan J ^a   Stanforth, Stephen P ^a   Tarbit, Brian ^b  

^a NORTHUMBRIA UNIVERSITY   (United Kingdom)

^b Seal Sands Chemicals Ltd   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

HETEROCYCLIC COMPOUND; PALLADIUM;

ARTICLE; PRIORITY JOURNAL; REACTION ANALYSIS; SYNTHESIS;

LATEOLABRAX JAPONICUS;

EID: 0033601456     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4020(99)00961-8     Document Type: Article

References (11)

1. Stanforth, S. P. Tetrahedron, 1998, 54, 263 and references therein.
2. Undheim, K.; Benneche, T. Adv. Heterocycl. Chem., 1995, 62, 305.
3. Coad, P.; Coad, R. A.; Clough, S.; Hyepock, R.; Salisbury, R.; Wilkins, C. J. Org. Chem., 1963, 28, 218.
4. Heinisch, G.; Holzer, W. Can. J. Chem., 1991, 69, 972.
5. Steiner, G.; Gries, J.; Lenke, D. J. Med. Chem., 1981, 24, 59.
6. Barlin, G.; Aust. J. Chem., 1986, 39, 1803.
7. 3-Chloro-6-arylpyridazines are generally prepared from their corresponding 6-aryl-3(2H)-pyridazinones. See for example: Hallot, A.; Brodin, R.; Merlier, J.; Brochard, J.; Chambon, J. -P.; Biziere, K. J. Med. Chem., 1986, 29, 369; Srinivasan, T. N.; Rama Rao, K.; Sattur, P. B. Synth. Commun., 1986, 16, 543.
8. 3-Chloro-6-arylpyridazines are generally prepared from their corresponding 6-aryl-3(2H)-pyridazinones. Seefor example: Hallot, A.; Brodin, R.; Merlier, J.; Brochard, J.; Chambon, J. -P.; Biziere, K. J. Med. Chem., 1986, 29, 369; Srinivasan, T. N.; Rama Rao, K.; Sattur, P. B. Synth. Commun., 1986, 16, 543.
9. Ohsawa, A.; Abe, Y.; Igeta, H. Chem. Pharm. Bull., 1980, 28, 3488.
10. Plé, N.; Turck, A.; Heynderickx, A.; Quéguiner, G. J. Heterocycl. Chem., 1997, 34, 551.
11. Minato, A.; Suzuki, K.; Tamao, K.; Kumada, M. J. Chem. Soc., Chem. Commun., 1984, 511.