Collect. Czech. Chem. Commun.
2006, 71, 1453-1469
https://doi.org/10.1135/cccc20061453
DFT Study on 3-Substituted Tetrahydropyran-2-yl Radicals
Stanislav Kozmon and Igor Tvaroška*
Institute of Chemistry, Slovak Academy of Sciences, 845 38 Bratislava, Slovakia
References
1. Adv. Carbohydr. Chem. Biochem. 2001, 56, 65.
< J.-P.: https://doi.org/10.1016/S0065-2318(01)56003-5>
2. Angew. Chem., Int. Ed. Engl. 1989, 28, 969.
< B.: https://doi.org/10.1002/anie.198909693>
3. Top. Curr. Chem. 1997, 187, 1.
< J.-M., Gallagher T.: https://doi.org/10.1007/BFb0119252>
4. Synlett 1998, 700.
< H., He W., Waki Y., Yokoyama M.: https://doi.org/10.1055/s-1998-1753>
5. J. Am. Chem. Soc. 1988, 110, 8716.
< D., Yang D., Lim J. J., Miller R., Paguaga E.: https://doi.org/10.1021/ja00234a034>
6. Adv. Carbohydr. Chem. Biochem. 1991, 49, 37.
< L., Ferrier R. J.: https://doi.org/10.1016/S0065-2318(08)60181-X>
7. Chem. Rev. 2001, 101, 81.
< L.: https://doi.org/10.1021/cr980007n>
8. Acc. Chem. Res. 1989, 22, 152.
< T., Ghupathy M.: https://doi.org/10.1021/ar00160a006>
9. Adv. Carbohydr. Chem. Biochem. 1989, 47, 45.
< I., Bleha T.: https://doi.org/10.1016/S0065-2318(08)60412-6>
10. J. Chem. Soc., Perkin Trans. 2 1986, 1453.
< H.-G., Sustmann R., Dupuis J., Giese B.: https://doi.org/10.1039/p29860001453>
11. Chem. Ber. 1990, 123, 1155.
< H.-G., Praly J.-P., Somsák L., Sustmann R.: https://doi.org/10.1002/cber.19901230532>
12. Aust. J. Chem. 1971, 24, 2099.
< A. L. J., Tindal P. K.: https://doi.org/10.1071/CH9712099>
13. J. Chem. Soc. A 1971, 124.
< A. J., Gilbert B. C., Norman R. O. C.: https://doi.org/10.1039/j19710000124>
14. J. Chem. Soc., Perkin Trans. 2 1980, 647.
< B. C., Norman R. O. C., Williams P. S.: https://doi.org/10.1039/p29800000647>
15. Tetrahedron 1998, 54, 4623.
< A. L. J., Duggan P. J.: https://doi.org/10.1016/S0040-4020(98)00178-1>
16. Tetrahedron 1998, 54, 6919.
< A. L. J., Duggan P. J.: https://doi.org/10.1016/S0040-4020(98)00373-1>
17. J. Am. Chem. Soc. 1992, 114, 8375.
< S. D., Powers J. P., LePage T.: https://doi.org/10.1021/ja00048a005>
18. Tetrahedron 2001, 57, 477.
< A., Whitfield D., Nukada T. M.: https://doi.org/10.1016/S0040-4020(00)01019-X>
19. J. Mol. Struct. 1997, 395–396, 1.
< I., Carver J. P.: https://doi.org/10.1016/S0166-1280(96)04674-X>
20. Adv. Magn. Reson. 1977, 9, 1.
< P. D., Menger E. M.: https://doi.org/10.1016/B978-0-12-025509-2.50006-3>
21. ADF2004.01, SCM. Theoretical Chemistry, Vrije Universiteit, Amsterdam 2004; http://www.scm.com.
22. J. Theor. Chim. Acta 1998, 99, 391.
< C., Snijders J. G., te Velde G., Baerends E.: https://doi.org/10.1007/s002140050021>
23. J. Comput. Chem. 2001, 22, 931.
< G., Bickelhaupt F. M., van Gisbergen S. J. A., Fonseca Guerra C., Baerends E. J., Snijders J. G., Ziegler T.: https://doi.org/10.1002/jcc.1056>
24. Parallel Quantum Solutions. 2013 Green Acres, Suite A, Fayetteville, AR 72703, U.S.A.
25. Can. J. Phys. 1980, 58, 1200.
< S. H., Wilk L., Nusair M.: https://doi.org/10.1139/p80-159>
26. Phys. Rev. 1988, 38, 3098.
< A. D.: https://doi.org/10.1103/PhysRevA.38.3098>
27. Phys. Rev. B 1986, 33, 8822.
< J. P.: https://doi.org/10.1103/PhysRevB.33.8822>
28. J. Chem. Soc., Perkin Trans. 2 1993, 799.
< A., Schüürmann G.: https://doi.org/10.1039/p29930000799>
29. J. Phys. Chem. 1995, 99, 2224.
< A.: https://doi.org/10.1021/j100007a062>
30. J. Chem. Phys. 1996, 105, 9972.
< A., Jones V.: https://doi.org/10.1063/1.472829>
31. Jaguar 5.5, release 11. Schrödinger, Inc., Portland (OR) 2004.
32. J. Chem. Phys. 1993, 98, 5648.
< A. D.: https://doi.org/10.1063/1.464913>