By Alan R. Katritzky
Chapters of this quantity take care of heavily similar tricyclic heteromatic platforms. The final accomplished overview of the dibenzofurans seemed in 1951; the topic is now up-to-date via Sargent and Stransky. Carbazoles have additionally no longer been comprehensively reviewed lately; this has been performed during this quantity by means of Joule.The chemistry of 4-membered earrings containing one sulfur atom — the thietanes and their derivatives — is roofed via Ried and Heinz, who replace prior surveys that seemed approximately two decades ago.The bipyridines, of substantial commercial and theoretical curiosity, are comprehensively reviewed for the 1st time via Summers.Two chapters, facing 2H- and 4H- imidazoles through Sammes and the sequence editor, proceed and finish the sequence on nonaromatic azoles, which incorporated 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 conceal the literature up via 1982.
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Extra info for Advances in Heterocyclic Chemistry, Vol. 35
Zahorsky, D. Maassen. and 1. Seeger, Chem. Ber. 96. 1579 (1963). 7 4 N. E. Stjernstrom, Ark. Kemi 21, 57 (1963). " S. Shibata, Acta Phytochim. 14, 9 (1944) [CA 45, 7100 (195l)l. 7 6 H. Musso, Chem. Ber. 91, 349 (1958). 7 7 C. A. Wachtrneister, Acta Chem. Srand. 12, 147 (1958). 78 D. 0. Chester and J. A. Elix, Aust. J. Chem. 34, 1501 (1981). ''C. A. Wachtmeister, Acta Chem. Scand. 8, 1433 (1954). B. Akermark, H. Erdtman, and C. A. Wachtrneister, Acta Chem. Scand. 13, 1853 (1959). C. J. R. Adderley and F.
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. By Ullmann-Type Synthesis Baker and co-workers" observed during the synthesis of the biphenyl 74 (Scheme 19) from the iodo compound 73 by the Ullmann reaction at 230°C with copper bronze in nitrobenzeiie that the dibenzofuran 75 (1%) M e o Me0 ~ ~ Br rM e 0 m Br M- -O e + Me Me0 Me0 OMe (73) (74) c1 \ / \ ,/ OMe (75) CI (78) C1 (79) SCHEME 19 Puskas, E.
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). '* H. Erdtman, F. Haglid, and N. E. Stjernstrom, Acta Chetn. Scand. 15, 1761 (1961). 7 3 H. Musso, U. 1. Zahorsky, D. Maassen. and 1. Seeger, Chem. Ber. 96. 1579 (1963). 7 4 N. E. Stjernstrom, Ark. Kemi 21, 57 (1963).
Advances in Heterocyclic Chemistry, Vol. 35 by Alan R. Katritzky