Synthesis of diacyl disulfides using a polymer supported reagent

Synthetic Communications

Volumn 28, Issue 7, 1998, Pages 1275-1280

  Tamami, B ^a   Kiasat, A R ^a  

^a SHIRAZ UNIVERSITY   (Iran)

Author keywords

[No Author keywords available]

Indexed keywords

DISULFIDE; POLYMER;

INFRARED SPECTROMETRY; PROTON NUCLEAR MAGNETIC RESONANCE; REACTION ANALYSIS; REVIEW; SYNTHESIS;

EID: 0031920879     PISSN: 00397911     EISSN: None     Source Type: Journal    
DOI: 10.1080/00397919808005969     Document Type: Review

References (13)

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3. a) Gladysz, J.A., Vistor K. Wang and Bryan S. Jick, J. Chem. Soc., Chem. Commun., 1978, (19), 838.
4. b) Gladysz, J.A., Vistor K. Wang and Bryan S. Jick, Tetrahedron, 1979, 35, 2329.
5. Chokravarit, G.C. J. Indian Chem. Soc., 1928, 5, 405.
6. Kodomari, M., Fukuda, M. and Yoshitomi, S., Synthesis, 1981, 8, 637.
7. Wang, J.X. Cui, W. Hu, Y. and K., Zhao, Synth. Commun. 1995, 25(6), 889.
8. a) Sherrington, D.C. and Hodge, P. "Synthesis and Separation Using Functional Polymers" Wley, Chichester 1988.
9. b) Takamuto, K., Inaki, Y. and Ottennbrite, R.M. "Functional Monomers and polymers, Procedures, Synthesis and Applications" Marcel Dekker, Inc., New York 1987.
10. c) Akelah, A. and Sherrington, D.C. Polymer 24, 1369, 1983.
11. d) Mckillop, A. and Yound, D.W. Synthesis, 401, 1979.
12. Deng T. and Chen. J.Y., Chem. Abstract, 108: 227489 P.
13. Polymer supported reagent has to be used in the wet form. It will slowly lose its activity if dried.