Synthesis and characterization of 2,2-disubstituted thiadiazolines

Arkivoc

Volumn 2000, Issue 4 SPEC.ISS., 2000, Pages 627-640

  Martins Alho, M A ^a   Moglioni, A G ^a   Brousse, B ^a   Moltrasio, G Y ^a   D'Accorso, N B ^a  

^a UNIVERSIDAD DE BUENOS AIRES   (Argentina)

Author keywords

[No Author keywords available]

Indexed keywords

3,4 DIHYDRONAPHTHALEN 1(2H) ONE THIOSEMICARBAZONE; 3,4' DIMETHOXYBENZOPHENONE THIOCARBAMAZONE; 4 METHOXYBENZOPHENONE THIOCARBAMAZONE; 4,4' DIMETHOXYBENZOPHENONE THIOCARBAMAZONE; 5 ACETAMIDO 3 N ACETYL 2 (3',4' DIMETHOXYPHENYL) 2 PHENYL 1,3,4 THIADIAZOLINE; 5 ACETAMIDO 3 N ACETYL 2 (4' METHOXYPHENYL) 2 PHENYL 1,3,4 THIADIAZOLINE; 5 ACETAMIDO 3 N ACETYL 2,2 BIS(4' METHOXYPHENYL) 1,3,4 THIADIAZOLINE; 5 ACETAMIDO 3 N ACETYL 2,2 DIPHENYL 1,3 THIADIAZOLINE; 5 METHOXYINDAN 1 ONE THIOSEMICARBAZONE; 6 METHOXYINDAN 1 ONE THIOSEMICARBAZONE; ANTHRONE THIOSEMICARBAZONE; ANTIFUNGAL AGENT; ANTIINFECTIVE AGENT; HETEROCYCLIC COMPOUND; HYDROGEN; INDAN 1 ONE THIOSEMICARBAZONE; KETONE DERIVATIVE; SPIRO[5 ACETAMIDO 3 N ACETYL 2,1' (1',2',3',4' TETRAHYDRONAPHTHALEN)] 1,3,4 THIADIAZOLINE; SPIRO[5 ACETAMIDO 3 N ACETYL 2,1' (5' METHOXYINDAN)] 1,3,4 THIADIAZOLINE; SPIRO[5 ACETAMIDO 3 N ACETYL 2,1' (6' METHOXYINDAN)] 1,3,4 THIADIAZOLINE; SPIRO[5 ACETAMIDO 3 N ACETYL 2,1' INDANE] 1,3,4 THIADIAZOLINE; THIADIAZOLE DERIVATIVE; THIOSEMICARBAZONE DERIVATIVE; UNCLASSIFIED DRUG;

CARBON NUCLEAR MAGNETIC RESONANCE; CHEMICAL STRUCTURE; CONFERENCE PAPER; DRUG SYNTHESIS; MASS SPECTROMETRY; PROTON NUCLEAR MAGNETIC RESONANCE;

EID: 0005850113     PISSN: 14246376     EISSN: 14246376     Source Type: Journal    
DOI: None     Document Type: Conference Paper

References (16)

1. Leafe E. L., Chem. Abstr., 64, 1279b (1966): Proc. Brit. Weed Control Conf., 7th, 32 (1964).
2. Leafe E. L., Chem. Abstr., 64, 1279b (1966): Proc. Brit. Weed Control Conf., 7th, 32 (1964).
3. Bhat A. K., Bhamaria R. P., and Bellare R. A., Indian J. Chem., 5, 1279 (1967).
4. Zsolnai T., Chem. Abstr., 57, 6431 (1962): Biochem. Pharmacol., 11, 271 (1962).
5. Zsolnai T., Chem. Abstr., 57, 6431 (1962): Biochem. Pharmacol., 11, 271 (1962).
6. Thakar K. A. and Bhawal B. M., J. Indian Chem. Soc., 54, 875 (1977).
7. a) Holmberg B., Arkiv. Kemi, 7, 517 (1954).
8. b) Sandströn J., Adv. Heterocycl., 9, 165 (1968).
9. Evans D. and Taylor D. R., J. Chem. Soc. Chem. Comm., 188 (1982).
10. Martins Alho M. A. and D'Accorso N. B., J. Heterocyclic Chem., 34, 1415 (1997).
11. Andreae S., Schmitz E., and Seeboth H., Journal f. prakt. Chemie, 328, 205 (1986).
12. Somogyi L., Tetrahedron, 47, 9305 (1991).
13. Kubota S., Ueda Y., Fujikane K., Toyooka K., and Shibuya M., J. Org. Chem., 45, 1473 (1980).
14. Martins Alho M. A., Moglioni A. G., Brousse B., Moltrasio Iglesias G. Y., and D'Accorso N. B., 17th International Congress of Heterocyclic Chemistry, Vienna, Austria, August 1-6, 1999.
15. Tarbell D. S. and Price J. A., J. Org. Chem., 22, 245 (1957).
16. Dictionary of Organic Compounds on CD-ROM. Chapman&Hall. Version 6.2. September 1998.