H. Sauge, J. P. Lacroze, J. L. Poëssel, T. Pascal, and J. Kervella, Induced resistance by Myzus persicae in the peach cultivar 'Rubira', Entomologia Experimentalis et Applicata, vol.102, issue.1, pp.29-37, 2002.
DOI : 10.1046/j.1570-7458.2002.00922.x

C. Sinisi, N. Forzato, L. Cefarin, F. Navarini, and . Berti, Interaction of chlorogenic acids and quinides from coffee with human serum albumin, Food Chemistry, vol.168, p.332, 2015.
DOI : 10.1016/j.foodchem.2014.07.080

. Hz, 76 (s, 1H, OH 1 ), 3.74 (s H 4a ); 13 C NMR (CDCl 3 , 298K, 125 MHz) ? (ppm) = 175, 12H, OCOCH 3 ), 2.32 (m, 1H, H 4 ), 2.23-2.18 (m, 2H, H 2 and H 6 ), 2.08-2.00 (m, 2H, H 2 and H 6 ), 1.87 (ddd, 1H 165.8 and 165.5 (2xCOO), 143.59 and 143.57 (C q ), 143.3 and 143.2 (CH=CHCO) , 142.5 and 142 122.9 and 122.8 (C 2' ), 119.4 and 119.2 (CH=CHCO) HRMS-ESI m/z [M+Na] + calcd for C 34 H 34 NaO 15 705, pp.39-46, 1790.

4. Arm, 2. , and C. Ar, 1067 cm -1 ; 1 H NMR (CDCl 3, 298K, 300MHz) ? (ppm) = 7.63 and 7.58 (2d, 2H, 3 J 15.9 Hz, CH=CHCO) 2H, H 3 and H 5 ), 5.42-5.39 (m, 2H, CH 2 anti=CHCH 2 O), 5.30 (m, 4H, CH 2 syn =CHCH 2 O), 4.64 (m, 8H, CH 2 =CHCH 2 O), 2.32 (m, 1H, H 2 or H 4 or H 6 ) MHz) ? (ppm) =, pp.89-91, 1090.

H. Hz, 2. Meta-oacdd, and 3. , 1 Hz, H orthoOAc), 6.46 and 6, pp.5-537513

. Hz, H-4); 13 C NMR (CDCl 3 , 295K, 100 MHz) ? (ppm) = 175.0 (COOMe), 169.45 and 169, 165.8 and 165.6 (COO), pp.138-56

C. Hz, 42 (m, 2H, H 3 and H 5 ), p.46

. Hz, ), 9 Hz, H 2 or H 6 ) C NMR (CD 3 OD, 298K, 125 MHz) ? (ppm) =, p.97

K. P. Narender, G. Reddy, and . Madhur, NaOAc-Mediated Selective Deprotection of Aromatic Acetates and Its Application in the Synthesis of Natural Products, Synthetic Communications, vol.39, issue.11, pp.1949-1956, 2009.
DOI : 10.1021/ja00440a055

H. Hz, -170.0 (C 0.93, CH 3 OH) IR(ATR) 3516, The general procedure E for the deprotection of aromatic acetates was performed with 9c (65 mg DMF (0.45 mL) and hydrazine acetate (43 mg, 0.47 mmol) providing after purification 10c as a colorless oil H NMR (CD 3 OD, 400 MHz) : ? ppm = 7.63 and 7.57 (d, 2H, 3 J 15.9 Hz, CH=CHCO), 7.12 (bs, 2H, Ar-H), 7.07 (dd, 2H, J ortho 8,2 Hz, J meta 2,7 Hz, Ar-H), 6.81 (dd, 2H, J ortho 8 Hz, H 2 or H 6 ), 2.38 (dd, 1H, 2 J 13.6 Hz, 3 J 7.2 Hz, H 2 or H 6 ), 2.14-1.97 MHz) ? (ppm) = 175.7 ((COOMe), 168.4 and 168.0 (OCO) 147.1 and 147.0 (CH=CHCO), 127.7 and 127.5 (C q Ar ), 124.2 and 124.1 (CH Ar 39.8 and 39.2 (C 2 or C 6 ) HRMS-ESI m/z [M+Na] + calcd for C 28 H 30 NaO 11 65, pp.1009-1010, 1032.
URL : https://hal.archives-ouvertes.fr/hal-00069306

2. Hz and 4. Ch=chcod, 81 (dd, 4H, J ortho 8.6 Hz, J meta 1, 6.34 and 6.26 (d, 2H, 3 J 15.9 Hz, CH=CHCO), 5.43 (m, 2H, H 3 and H 5 ), 3.69 (s, 3H, OMe), 2.46 (dd, 1H 13 C NMR (CD 3 OD, 100 MHz) ? (ppm) = 175.7 (COOMe), pp.4740-146

H. Nmr, CD 3 OD, 298K, 400 MHz) : ? ppm = 7

C. Nmr, 100 MHz, 297K) ? (ppm) = 177, 168.5 and 168.3 (2xOCO), 161.12 and 161.07 (2xCq), 146.7 and 146, p.131

. Hz, 00 (m, 4H, H 2 , H 4 or H 6 ); 13 C NMR (CD 3 OD, 75 MHz, 297K) ? (ppm) = 177, 168.5 and 168 146.9 and 146.8 (2xCH=CHCO), 127.74 and 127 111.7 and 111.6 (2x CH=CHCO), pp.150-4438

C. Hz, 52 (dd, 4H, J ortho 8,6 Hz, J ortho 6.8 Hz

. Hz, H 6 and 2xOCOCH 3 ); 13 C NMR (CDCl 3 , 100 MHz) ? (ppm) = 177.0 (COOH), 169.41 and 169, pp.6-41

. Hz, 12H, 3xCH 3 ); 13 C NMR (100 MHz, CDCl 3 ) ? (ppm) = 168.15 and 168 C q Ar ), 133.1 and 133, COO), 144.03 and 143.98 (2 CH=CH), 143.82 and 143.77 (2 C q Ar ) 118.5 and 118 CH=CH), pp.81-82

C. Hz, 05 (dd, 2H, J 6.1 Hz, J 2.0 Hz, ArH), p.9477