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) 41, 807 (1972) 215 G Bouillon, C Lick, and K Schank, in The Chemistry of Peroxides, S Patai, ed, Wiley, Chichester, 10, p 279 216 B Plesnicar, in Oxidation in Organic Chemistry, Part C, W S Trahanovsky, ed, Academic Press, New York, 1978, 3, p 211 217 B Plesnicar, in The Chemistry of Peroxides, S Patai, ed, Wiley, Chichester, 1983, 17, p 521 218 M Bartok and K L Lang, in The Chemistry of Heterocyclic Compounds, A Weissberger and E C Taylor, eds, Vo!' 42: Small Ring Heterocycles, Part 3, A Hassner, ed, Wiley, New York, 1985, 1, p 1 219 A S Rao, S K Paknikar, and J G Kirtane, Tetrahedron 39,2323 (1983) 220 A S Rao, in Comprehensive Organic Synthesis, B M Trost and 1 Fleming, eds, Vo!' 7: Oxidation, S V Ley, ed, Pergamon Press, Oxford, 1991, 3.

dH(t) dW (8.89) = H H = 1 (t)H(t)][ (t) f [y(t)] gT [y(t)]], dt dt where = diag{ 1 , 2 , . . . , n } is a diagonal positive de nite matrix (typically, = In or = diag{f [y(t)] yT (t)}) and f [y(t)] = [f1 (y1 ), . . . , fn (yn )]T , g(y) = [g1 (y1 ), . . . , gn (yn )]T are vectors of suitably chosen nonlinear functions. We can replace the output vector y(t) by an improved estimate y(t) to derive a learning algorithm as dH(t) = 1 (t)H(t) (t) f [y(t)] gT [y(t)] dt and dy(t) = (t)HT (t) [e(t)], dt (8.91) (8.90)

If you group all your logo layers into a Logo group in the Layers palette, you only need to click the group s eye icon to toggle the visibility of all the layers in the group.

1, p 357 221 Y Sawaki, in The Chemistry of Functional Groups, Supplement E2: The Chemistry of Hydroxyl, Ether and Peroxide Groups, S Patai, ed, Wiley, Chichester, 1993, 11, p 587 222 H Heaney, Top Curro Chem 164, 1 (1993) 223 B M Lynch and K H Pausacker, l Chem Soc 1525 (1955) 224 G Berti, Top Stereochem 7, 93 (1973) 225 D J Goldsmith, l Am Chem Soc 84, 3913 (1962) 226 T Sato and E Murayama, Bull Chem Soc lpn 47, 1207 (1974) 227 H Kwart and D M Hoffman, l Org Chem 31, 419 (1966) 228 H-J Schneider, N Becker, and K Philippi, Chem Ber 114, 1562 (1981) 229 R D Bach, C L Willis, andJ M Domaglia, in Applications ofMO Theory in Organic Chemistry, 1 G Csizmadia, ed, Elsevier, Amsterdam, 1977, p 221 230 B Plesnicar, M Tasevski, and A Azman, l Am.

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Chem Soc 100, 743 (1978) 231 M S Stytilin, Russ l Phys Chem (Eng! trans!) 51, 284 (1977) 232 R M Makitra and Ya N Pirig, Russ l Phys Chem (Eng! trans!) 52,451 (1978) 233 J Skerjanc, A Regent, and B Plesnicar, l Chem Soc, Chem Commun 1007 (1980) 234 V G Dryuk, Tetrahedron 32,2855 (1976) 235 J G Traynham, G R Franzen, G A Knesel, and D J Northington, Jr, l Org Chem 32, 3285 (1967)..

5. Add a point to the curve, as described in 4, in the lower levels, and adjust it up a bit so the image is not so dark.

Note that the selection you made on the Blue channel is active in the composite RGB view as well. After selecting the major portion of the sky and mountain, add the peek-through areas (where the lower sections of the mountains peek through the tops of the vegetation).