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J. =d and J. , CHAr 1 -ortho or CHAr 1 -meta), 129.1 (CHAr 1 -ortho or CHAr 1 -meta), 128.0 (CHAr 1 -para), NMR (CDCl3, 100.6 MHz) ? 170CH3)3), 29.1 (C-(CH3)3), pp.55-62

J. Hzd and J. =d, 9 Hz, CHAr-meta), 63.3 (d, JC-P = 6.6 Hz, ), 55.7 (d, JC-P = 6.6 Hz cyclohexyl or CH2-6 cyclohexyl), 33.5 (CH2-2 cyclohexyl or CH2-6 cyclohexyl), pp.33-39

2. Hz, 1. Har-metam, O. , and N. , m, 2H, O-CH2-CH3 ; CH-1 cyclohexyl, pp.4-24

2. Hz and . Har-meta, 46 (s, 2H, ), 3.98 (dd, J = 5.5, 18.2 Hz, 1H, N-CH2-CO-OEt)8 Hz, 1H, CH-P), 1.80 (bs, 1H, CH-(CH3)2)), 1.34 (t, J = 7.0 Hz, 3H, P-(O-CH2-CH3)2), 1.33 (t, J = 7.0 Hz, 3H, P-(O-CH2-CH3)2), 1.29 (t, J = 7.1 Hz, 3H, CO-O-CH2-CH3), 0.91 (d, J = 6.6 Hz, 3H, CH-CH3), pp.4-17

1. Hz, m, 6H, HAr 1 -ortho,meta ; HAr 2 -meta, NMR (CDCl3, 400 MHz) ? 8.04 1H, HAr 1 -para), 6.94 (d, J = 8.3 Hz, 2H, HAr 2 -ortho), pp.45-52

N. Oet, 2. , and P. , 86 (s, 3H, O-CH3), 3, 3.28 (d, Jab = 13.1 Hz, 1H, N-CH2-Ph), 3.05 (d, Jab = 16.7 Hz 1.36 (t, J = 7.1 Hz, 3H, P-O-CH2-CH3), 1.29 (t, J = 7.1 Hz, 3H, P-O-CH2-CH3), 1.08 (t, J = 7.1 Hz, 3H, CO-O-CH2-CH3), pp.4-6