1,3-Dithiane polymers for the supported synthesis of ketones

Tetrahedron Letters

Volumn 39, Issue 50, 1998, Pages 9263-9266

  Bertini, Vincenzo ^a   Lucchesini, Francesco ^a   Pocci, Marco ^a   De Munno, Angela ^b  

^a UNIVERSITY OF GENOA   (Italy)

^b UNIVERSITY OF PISA   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

1,3 DITHIANE DERIVATIVE; KETONE DERIVATIVE; POLYMER; PROPANE 1,3 DITHIOL; UNCLASSIFIED DRUG;

ALKYLATION; ARTICLE; CARBON NUCLEAR MAGNETIC RESONANCE; INFRARED SPECTROSCOPY; PROTON NUCLEAR MAGNETIC RESONANCE; SOLID STATE; SYNTHESIS; TEMPERATURE;

EID: 0032506618     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(98)02081-4     Document Type: Article

References (20)

1. 1. Seebach, D., Corey, E. J. J. Org. Chem. 1975, 40, 231-237.
2. 3) ppm 168.8, 137.5, 136.5, 136.1, 129.0, 126.3, 113.5, 61.5, 53.8, 34.4, 14.0.
3. 3) ppm 139.6, 136.5, 135.6, 129.2, 126.3, 113.3, 65.3, 43.8, 34.0.
4. 3) ppm 136.8, 136,3, 136.2, 135.4, 134.0, 129.4, 129.1, 127.9, 126.5, 113.8, 68.4, 40.0, 32.9.
5. 3) ppm 195.2, 138.5, 136.5, 135.8, 129.3, 126.3, 113.4, 40.3, 38.8, 31.9, 30.6.
6. 6. Calculated from the molar ratio of the comonomers submitted to polymerization.
7. 7. a. The Aldrich Library of FT-IR Spectra, Pouchert, C. J. Ed. Aldrich Chemical Company: U.S.A., 1985, Vol. 2, 9C; b. ibid. 18C; c. ibid. 1B.
8. 7. a. The Aldrich Library of FT-IR Spectra, Pouchert, C. J. Ed. Aldrich Chemical Company: U.S.A., 1985, Vol. 2, 9C; b. ibid. 18C; c. ibid. 1B.
9. 7. a. The Aldrich Library of FT-IR Spectra, Pouchert, C. J. Ed. Aldrich Chemical Company: U.S.A., 1985, Vol. 2, 9C; b. ibid. 18C; c. ibid. 1B.
10. 8. a. The Aldrich Library of FT-NMR Spectra, Pouchert, C. J.; Behnke, J. Eds. Aldrich Chemical Company: U.S.A., 1993, Vol. 2, 803B; b. ibid. 822A; c. ibid. 789B.
11. 8. a. The Aldrich Library of FT-NMR Spectra, Pouchert, C. J.; Behnke, J. Eds. Aldrich Chemical Company: U.S.A., 1993, Vol. 2, 803B; b. ibid. 822A; c. ibid. 789B.
12. 8. a. The Aldrich Library of FT-NMR Spectra, Pouchert, C. J.; Behnke, J. Eds. Aldrich Chemical Company: U.S.A., 1993, Vol. 2, 803B; b. ibid. 822A; c. ibid. 789B.
13. 9. Kozikowski, A. P.; Ames, A. Tetrahedron 1985, 41, 4821-4834.
14. 10. Gronowitz, S.; Eriksson, B. Arkiv Kemi 1963, 31, 335-341.
15. 11. Okamoto, T.; Kakinami, T.; Nishimura, T. Bull. Chem. Soc. Jpn. 1992, 65, 1731-1733.
16. 12. Shuikin, N. I.; Ai-Hsi Yang; Erivanskaya, A. L. Izv. Akad. Nauk. SSSR, Ser. Khim. 1963, 1284-1289.
17. 3) ppm 138.5, 138.3, 129.2, 128.7, 128.6, 128.5, 127.8, 126.5, 51.4, 43.0, 37.6, 37.3.
18. 3) ppm 141.2, 138.6, 129.2, 128.6, 126.7, 126.5, 126.1, 125.6, 45.1, 42.2, 36.8, 36.7.
19. 15. Eliel, E. L.; Hutchins, R. O. J. Am. Chem. Soc. 1969, 91, 2703-2715.
20. 16. Haramoto, Y.; Kamogawa, H. Bull. Chem. Soc. Jpn. 1985, 58, 477-480.