Download Chemistry of Heterocyclic Compounds: Tellurium-Containing by Michael R. Detty PDF

By Michael R. Detty

Tellurium-Containing Heterocycles: experiences, Distinguishing positive factors, and Utility.

Tellurophenes, Dihydrotellurophenes, and Tetrahydrotellurophenes and Their Benzo and Dibenzo Analogs.

Telluranes, Tellurins, and different 6-membered earrings Containing One Tellurium Atom.

Telluropyrylium Compounds.

Tellurium-Containing Heterocycles with not less than One team Va aspect (Nitrogen, Phosphorus, or Arsenic).

Tellurium-Containing Heterocycles Composed of crew IVa (Carbon, Silicon, Germanium, and Tin) and team through parts (Tellurium, Selenium, Sulfur, and Oxygen).

Tellurium-Containing Heterocycles as Donor Molecules.

Tellurium-Containing Heterocycles with Hypervalent or Coordination Bonds to Tellurium (M. O'Regan).

Chapter I Tellurium?Containing Heterocycles: reports, Distinguishing positive aspects, and software (pages 1–30):
Chapter II Tellurophenes, Dihydrotellurophenes, and Tetrahydrotellurophenes and their Benzo and Dibenzo Analogs (pages 31–145):
Chapter III Telluranes, Tellurins, and different Six?Membered jewelry Containing one Tellurium Atom (pages 147–217):
Chapter IV Telluropyrylium Compounds (pages 219–291):
Chapter V Tellurium?Containing Heterocycles with at the least One team Va point (Nitrogen, Phosphorus, or Arsenic) (pages 293–324):
Chapter VI Tellurium?Containing Heterocycles Composed of workforce IVa (Carbon, Silicon, Germanium, and Tin) and crew through components (Tellurium, Selenium, Sulfur, and Oxygen) (pages 325–361):
Chapter VII Tellurium?Containing Heterocycles as Donor Molecules (pages 363–423):
Chapter VIII Tellurium?Containing Heterocycles with to Hypervalent or Coordination Bonds to Tellurium (pages 425–490):

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Additional resources for Chemistry of Heterocyclic Compounds: Tellurium-Containing Heterocycles, Volume 53

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24. Drago, R. S. J. Chem. Educ. 50,244. 25. Rundk, R. E. Rec. Chem. Prog. 1%2,50. 3677. 26. Sadekov, I. ; Rybalkina, L. ;Movshovich, D. Ya;Bulgarevich, S. ; Kogan, V. A. Uspekhi Khimii 1991,150, 1229. 27. ; Renson, M. Tetrahedron 1978,34,655. 28. Detty, M. ; Luss, H. R. J. Org. Chem. 48, 5149. 29. Detty, M. ; Murray, B. ; Smith, D. ; Zumbulyadis, N. J . Am. Chem. Soc. 1983,105, 875. 30. Detty, M. R. J . Org. Chem 1980,45,274. 31. Detty, M. ; McKelvey, J. ; Geer, S. M. J . Org. Chem. 1986, 51, 1692.

Thomas, H. T. Patent 4,584,258 (1986). 64. Detty, M. R; Fleming, J. C. Ado. Mat. 6,48. 65. Detty, M. ; Fleming, J. C. S. Patent 5, 300,385 (1994). 66. ; Kageyama. ;Endo. T. Jpn. Kokai Tokkyo Koho Jpn. Patent 62,257,890 [87,257,890] (1987); Chem Abstr. 1987, 107, 187518t. 67. Kellogg, R. ; Laganis, E. D. S. 549 (1991). 68. Detty, M. ; Henne, B. Heterocycles 1993, 35, 1149. 69. Burberry, M. ; Tutt, L. ; Detty, M. R. US. Patent 5, 256,620 (1992). 70. Detty, M. ; Murray, B. J. S. Patent 4,279,365 (1981).

Chem. Rudiochem. 1972, 15, 1. References 27 13. ; Aharon-Shalom, E. J. Am. Chem. Soc. 1982,104,1154. 14. ;Cowan, D. J. ,Chem. Commun. 1982,336. 15. ; Kok,. G. ;Cowan. D. J . Am. Chem. Soc. 1987,109,4115. 16. Bailey, A. B; McCullough, R. ; Mays, M. ; Cowan, D. ; Lerstrup, K. Synth. Met. 1988, 27,B425. 17. Detty, M. ; Murray, B. ; Perlstein, J. H. Tetrahedron Lett. 1983, 24, 1239. 18. Detty. M. ; Hassett. J. W; Murray, B. ; Reynolds, G. A. Tetrahedron 1985,45, 4853. 19. Detty. M. ; Murray, B. J. J .

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