A facile synthetic method of herbicidal 2,-dihydro-3-methylene-2-substituted - phenyl-1hisoindol-1-one derivatives

Synthetic Communications

Volumn 26, Issue 1, 1996, Pages 67-74

  Kim, Jae Nyoung ^a   Ryu, Eung K ^b  

^a Chonnam National University   (South Korea)

^b Korea Research Institute of Chemical Technology   (South Korea)

Author keywords

[No Author keywords available]

Indexed keywords

HERBICIDE; ISOINDOLE DERIVATIVE;

ARTICLE; DRUG SYNTHESIS; REACTION ANALYSIS;

EID: 0030069510     PISSN: 00397911     EISSN: None     Source Type: Journal    
DOI: 10.1080/00397919608003863     Document Type: Article

References (8)

1. Pissiotas, G., Moser, H. and Brunner, H. G., EP 420810 ; Chem. Abstr., 1991, 115, 71391g.
2. Elbe, H. L., Marhold, A., Luerssen, K., Santel, H. J., Schmidt, R. R. and Krauskopf, B., EP 403891 ; Chem. Abstr., 1991, 114, 207016c.
3. Saito, K., Hagiwara, K., Hara, T., Ishikawa, H., Inaba, H. and Sato, J., JP 63 39859 ; Chem. Abstr., 1988, 109, 37735p.
4. Pissiotas, G., Moser, H. and Brunner, H. G., EP 305333; Chem. Abstr., 1989, 111, 133984f.
5. Katritzky, A. R. and Kotali, A., Tetrahedron Lett., 1990, 31, 6781.
6. Kotali, A. and Tsoungas, P. G., Tetrahedron Lett., 1987, 28, 4321.
7. 7. 4-Chloro-2-fluoro-5-hydroxyaniline (5) was prepared from 4-fluorophenol in 5 steps in 31 % overall yield.
8. 8. For example, the reaction of 4a and 5 in acetic acid (reflux, 24 h) gave only 15% of 6a.