By Alan R. Katritzky
The newest quantity within the Advances in Heterocyclic Chemistry sequence
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Additional resources for Advances in Heterocyclic Chemistry, Vol. 58
Amidyl radicals are generated with visible light irradiation in a controlled and efficient radical chain reaction (Scheme 30). 5913) and with H-atom donors ( Y - H) reduction of the amidyl radical occurs with formation of the indicative Y-S-2-pyridyl products. As is the case with N-chloroamides, amidyl radicals with suitable positioned alkenes generated from N-hydro- 38 JOHN L. ESKER AND MARTIN NEWCOME ISec. B H 87 SCHEME 29 xypyridine-2-thione imidate esters undergo efficient 5-exo cyclization.
48 11. Four-Membered Heterocycles. . ...... 54 s4 3 . Molecular Structure of 2-Phenylbenzotellurazole . . . . . 2. Reactions . . . . . . . . . . . . . . . . . . . . . . . . 3. Molecular Structure . . . . . . . . . . . . . . . . . . . . E. 1. . . . . . . . . . . . . . . . . . . F. 1,3-Thiatelluroles G. I ,2-Ditelluroles . 62 63 64 ............ .. A. 1-Hetera-2(3)(4)-telluracyclohexanes .
M. E. Kuehne and D. A. Horne. J . Org. Chem. 40, 1287 (1975). C. J . Michejda and D. H. Campbell, J . Am. Chem. Soc. 98,6728 (1976). C. J . Michejda and D. H. Campbell. , 577 (1977). P. Mackiewicz, R. Furstoss, B. Wagell, R. Cote. and J . Lessard. J . Org. Chem. 43, 3746 (1978). J . Lessard, R. Cote, P. Mackiewicz, R. Furstoss. and B. Wagell. J . Org. Chern. 43, 3750 (1978). C. J. Michejda. D. H. Campbell, D. H. Sieh, and S . R. Koepke, in “Organic Free Radicals” (W. A. ). Chapter 18. Am. Chem.