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 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 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 jewelry 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 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 structures 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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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.
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Extra resources for Compr. Heterocyclic Chem. III Vol. 3 Five-membered Rings with One Heteroatom
The authors hope to be excused for not covering the material in detail it deserves due to lack of room, for omitting many excellent papers and that the chapter is not free from the inevitable influence of authors’ personal visions, interests, tastes, and understanding. 1 Thermal and Photochemical Reactions The thermal reactions (unimolecular isomerization, decomposition, and annulation) of pyrrole and its benzoannulated derivatives, indole and carbazole, have been extensively studied both experimentally (by shock-wave technique over the temperature range of 1050–1800 K <1989JPC5802, 1991IJK733, 1997PCA7787, 2003MI231>, continuous-flow pyrolysis (CFP) <2000ARK576>, infrared laser powered homogeneous pyrolysis (IR LPHP) <2004NJC606>, laser-induced thermal desorption with Fourier-transform mass spectrometry <1997POL3197>, and flash vacuum pyrolysis <1997J(P1)2195, 1997J(P1)2203, 1999J(P1)2047, 2006ARK89, and references therein>) and theoretically <1998PCA10880, 1999CPL(300)321, 1999PCA3917, 1999PCA3923, 1999JMT(461)569, 2001PCA3605, 2001PCP2467, 2003PCA5427>, and also because of the important role that pyrrolic systems play as sources of precursors of the oxides of nitrogen (NOx), atmospheric pollutants, in the combustion of coals and other heavy fuels <1995MI507, 2002MI2317>.
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