Compr. Heterocyclic Chem. III Vol.13 Seven-membered by Katritzky A.R., et al. (eds.)

By Katritzky A.R., et al. (eds.)

Content material: v. 1. 3-membered heterocycles, including all fused structures containing a 3-membered heterocyclic ring / quantity editor, Albert Padwa -- v. 2. 4-membered heterocycles including all fused platforms containing a 4-membered heterocyclic ring / quantity editor, Christian Stevens -- v. three. 5-membered jewelry with one heteroatom including their benzo and different carbocyclic-fused derivatives / quantity editors, Gurnos Jones, Christopher A. Ramsden -- v. four. 5-membered jewelry with heteroatoms, every one with their fused carbocyclic derivatives / quantity editor, John Joule -- v. five. 5-membered earrings: triazoles, oxadiazoles, thiadiazoles and their fused carbocyclic derivatives / quantity editor, Viktor V. Zhdankin -- v. 6. different 5-membered jewelry with 3 or extra heteroatoms, and their fused carbocyclic derivatives / quantity editor, Viktor V. Zhdankin -- v. 7. 6-membered earrings with one heteroatom, and their fused carbocyclic derivatives / quantity editor, David StC. Black -- v. eight. 6-membered earrings with heteroatoms, and their fused carbocyclic derivatives / quantity editor, R. Alan Aitken -- v. nine. 6-membered earrings with 3 or extra heteroatoms, and their fused carbocyclic derivatives / quantity editor, Kenneth Turnbull -- v. 10. Ring platforms with a minimum of fused heterocyclic 5- or 6-membered jewelry with out bridgehead heteroatom / quantity editor, Ray C.F. Jones -- v. eleven. Bicyclic 5-5 and 5-6 fused ring structures with no less than one bridgehead (ring junction) N / quantity editor, Janine Cossy -- v. 12. 5- and 6-membered fused platforms with bridgehead (ring junction) heteroatoms concluded: 6-6 bicyclic with one or N or different heteroatoms; polycyclic; spirocyclic / quantity editor, Keith Jones -- v. thirteen. 7-membered heterocyclic earrings and their fused derivatives / quantity editor, George R. Newkome -- v. 14. 8-membered and bigger heterocyclic jewelry and their fused derivatives, different 7-membered earrings / quantity editor, George R. Newkome -- v. 15. Cumulative topic index

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P. White, K. K. Hii, P. N. Horton, and M. B. Hursthouse, J. Org. , 2005, 70, 1545. T. Taniguchi, A. Ishita, M. Uchiyama, O. Tamura, O. Muraoka, G. Tanabe, and H. Ishibashi, J. Org. , 2005, 70, 1922. S. Madan, P. Milano, D. B. Eddings, and R. E. Gawley, J. Org. , 2005, 70, 3066. C. E. J. Cordonier, K. Satake, M. Atarashi, Y. Kawamoto, H. Okamoto, and M. Kimura, J. Org. , 2005, 70, 3425. T. Ikemoto, T. Ito, A. Nishiguchi, S. Miura, and K. Tomimatsu, Org. Process Res. , 2005, 9, 168. T. Yamanaka, M.

Taguchi, and K. Honda, Chem. , 1996, 1621. 1996CC2257 M. Grellier and M. Pfeffer, Chem. , 1996, 2257. 1996CHEC-II(9)1 D. J. Le Count; in ‘Comprehensive Heterocyclic Chemistry II’, A. R. Katritzky, C. W. Rees, and E. F. V. ; Pergamon, Oxford, 1996, vol. 9, p. 1. 1996LA887 D. Kowalski, G. Erker, and S. , 1996, 887. B-1996MI(56)1 G. R. Proctor and J. , Chichester, 1996; vol. 56, p. 1. 1996T10883 D. Hamprecht, J. Josten, and W. Steglich, Tetrahedron, 1996, 52, 10883. 1996T14801 S. Kloetgen, R. -U. Wuerthwein, Tetrahedron, 1996, 52, 14801.

Hursthouse, J. Org. , 2005, 70, 1545. T. Taniguchi, A. Ishita, M. Uchiyama, O. Tamura, O. Muraoka, G. Tanabe, and H. Ishibashi, J. Org. , 2005, 70, 1922. S. Madan, P. Milano, D. B. Eddings, and R. E. Gawley, J. Org. , 2005, 70, 3066. C. E. J. Cordonier, K. Satake, M. Atarashi, Y. Kawamoto, H. Okamoto, and M. Kimura, J. Org. , 2005, 70, 3425. T. Ikemoto, T. Ito, A. Nishiguchi, S. Miura, and K. Tomimatsu, Org. Process Res. , 2005, 9, 168. T. Yamanaka, M. Ohkubo, M. Kato, Y. Kawamura, A. Nishi, and T.

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