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 platforms containing a 3-membered heterocyclic ring / quantity editor, Albert Padwa -- v. 2. 4-membered heterocycles including all fused structures containing a 4-membered heterocyclic ring / quantity editor, Christian Stevens -- v. three. 5-membered earrings with one heteroatom including their benzo and different carbocyclic-fused derivatives / quantity editors, Gurnos Jones, Christopher A. Ramsden -- v. four. 5-membered earrings with heteroatoms, each one with their fused carbocyclic derivatives / quantity editor, John Joule -- v. five. 5-membered jewelry: 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 jewelry with 3 or extra heteroatoms, and their fused carbocyclic derivatives / quantity editor, Kenneth Turnbull -- v. 10. Ring structures 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 at the very least 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 jewelry and their fused derivatives / quantity editor, George R. Newkome -- v. 14. 8-membered and bigger heterocyclic earrings and their fused derivatives, different 7-membered jewelry / quantity editor, George R. Newkome -- v. 15. Cumulative topic index

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

Content material: v. 1. 3-membered heterocycles, including all fused platforms containing a 3-membered heterocyclic ring / quantity editor, Albert Padwa -- v. 2. 4-membered heterocycles including all fused structures containing a 4-membered heterocyclic ring / quantity editor, Christian Stevens -- v. three. 5-membered earrings with one heteroatom including their benzo and different carbocyclic-fused derivatives / quantity editors, Gurnos Jones, Christopher A. Ramsden -- v. four. 5-membered earrings with heteroatoms, each one with their fused carbocyclic derivatives / quantity editor, John Joule -- v. five. 5-membered jewelry: 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 jewelry with 3 or extra heteroatoms, and their fused carbocyclic derivatives / quantity editor, Kenneth Turnbull -- v. 10. Ring structures 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 at the very least 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 jewelry and their fused derivatives / quantity editor, George R. Newkome -- v. 14. 8-membered and bigger heterocyclic earrings and their fused derivatives, different 7-membered jewelry / quantity editor, George R. Newkome -- v. 15. Cumulative topic index

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Jeong, W. S. Lee, S. Goto, S. Sano, M. Shiro, and Y. Nagao, Tetrahedron, 1998, 54, 14437. 1998TL2667 A. D. Piscopio, J. F. Miller, and K. , 1998, 39, 2667. 1999H(51)141 T. Tomita, H. Ishiguro, and K. Saito, Heterocycles, 1999, 51, 141. 1999JOC1849 T. Schertz, T. D. Lash, J. C. Petryka, R. C. Reiter, and C. D. Stevenson, J. Org. , 1999, 64, 1849. 1999J(P1)1695 C. A. Tarling, A. B. Holmes, R. E. Markwell, and N. D. Pearson, J. Chem. , Perkin Trans. 1, 1999, 1695. 1999MPH370 J. Setyawan, K. Koide, T.

Abbadie, J. P. Felix, M. L. Garcia, X. Li, K. A. Lyons, E. McGowan, D. E. MacIntyre, W. J. Martin, B. T. Priest, A. Ritter, M. M. Smith, V. A. Warren, B. S. Williams, G. J. Kaczorowski, and W. H. Parsons, Bioorg. Med. Chem. , 2007, 17, 4630. V. Declerck, P. Ribiere, Y. Nedellec, H. Allouchi, J. Martinez, and F. Lamaty, Eur. J. Org. , 2007, 201. U. Wirt, D. Schepmann, and B. Wunsch, Eur. J. Org. , 2007, 462. V. Singh and S. Batra, Eur. , 2007, 2970. D. Boeglin, D. Bonnet, and M. Hibert, J. Comb.

3-Benzoxepine reacts (Scheme 3) with deuterated dimethyldioxirane at À50  C in acetone-d6 to give respective 2,3-oxide, which between 5 and 10  C undergoes rapid ring-opening rearrangement to its isomer, 1H-2-benzopyran-1-carbaldehyde. Oxepanes and Oxepines Scheme 3 By 1H NMR monitoring of the oxidation of benzene oxide–oxepine with dimethyldioxirane (DMDO), a significant by-product, oxepine 4,5-dioxide, was identified <1997CRT1314>. This fact supports the hypothesis that the route from oxepine to muconaldehyde proceeds via oxepine 2,3-oxide with a minor pathway leading to symmetrical oxepine 4,5-oxide.

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