Download PDF by Alan R. Katritzky: Advances in Heterocyclic Chemistry, Vol. 35

By Alan R. Katritzky

ISBN-10: 0120206358

ISBN-13: 9780120206353

Chapters of this quantity care for heavily similar tricyclic heteromatic platforms. The final entire assessment of the dibenzofurans seemed in 1951; the topic is now up to date by means of Sargent and Stransky. Carbazoles have additionally no longer been comprehensively reviewed lately; this has been performed during this quantity by way of Joule.The chemistry of 4-membered jewelry containing one sulfur atom — the thietanes and their derivatives — is roofed by way of Ried and Heinz, who replace past surveys that seemed approximately two decades ago.The bipyridines, of substantial commercial and theoretical curiosity, are comprehensively reviewed for the 1st time by way of Summers.Two chapters, facing 2H- and 4H- imidazoles by way of Sammes and the sequence editor, proceed and finish the sequence on nonaromatic azoles, which integrated contributions on 2H- and 3H- pyrroles (in quantity 33) and on 3Н- and 4H- pyrazoles (in quantity 34).Most of the chapters during this quantity disguise the literature up via 1982.

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Lo' lo' lo' A. J. Copson, H. Heaney, A. A. Logun, and R. P. Sharma, JCS Chem. , 315 (1972). L. Mascarelli and M. Pirona, Gazz. Chim. Itul. 68, 117 (1938). F. Ullmann and W. Denzler, Ber. Dtsch. Chem. Ges. 39,4332 (1906). D. S. Tarbell, H. R. Frank, and P. E. Fanta, J . Ant. Chrm. 68, 502 (1946). P. E. Fanta, J . Am. Chern. Soc. 70, 4602 (1948). A. N. Nesmeyanov and T. P. Tolstaya, Izu. Akud. Nauk SSSR, Otd. Khim. Nauk, 647 (1959) [ C A 53, 21796 (1959)l Sec. B] 27 DIBENZOFURANS 4. 64*'l o 5.

R. Buser, Chmosphrre 9, 351 (1980). J. W. Engelsma and E. C. Kooyman, Reel. Trau. Chim. Pays-Bus 80,526 (1961). " R. 66 61 B. G. Pring and N. E. Stjernstrorn, Acta Chem. Scand. 22, 68 I (1968). N. P. Buu-Hoi, L. Petit, and D. C. Thang, J . Org. Chem. 29, 762 (1964). 69 E. Miiller, R. Mayer, B. Narr, A. Rieker, and K. Scheffler, Justus Liebigs Ann. Chem. 645, 25 (1961). 7 0 E. Pettersson and N. E. Stjernstrom, Ark. Kemi 21, 49 (1963). 7 1 B. G. Pring and N. E. Stjernstrom, A d a Chem. Scund. 22, 538 (1968).

W. Dawkins, and J. Ward, J. Chem. , 429 ( I 954). Sec. ’ 2 3 3. ’ to dibenzofuran by lithium aluminum hydride reduction and subsequent dehydrogenation, to 1-methyldibenzofuran by Grignard reaction and dehydrogenation, and to 1-dibenzofuranol by reaction with N-bromosuccinimide and subsequent dehydrobromination with pyridine. Benzofuran-2-carbaldehydes readily undergo Wittig reactions in tetrahydrofuran at room temperature with the resonance-stabilized ylide 2-carboxy- 1-methoxycarbonylethyltriphenylphosphorane,affording high yields of (E)-4-(2-benzofuranyI)-3-methoxycarbonylbut-3-enoic acids.

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Advances in Heterocyclic Chemistry, Vol. 35 by Alan R. Katritzky


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