C. , AcOEt 75:25 to yield the corresponding ?,?-diene monomer

, Bis-Allyl-O-Dihydroferuloyl, vol.1, p.4

, UV: ? max (EtOH): 211, 230, 281 nm. FTIR (neat): ? max, p.1510

(. C=c-ar, (2H, m, H 8 ), 6.69 (4H, m, H, vol.3

, CDCl, vol.3, issue.1

, Bis-Hexene-O-Dihydroferuloyl, vol.1, p.4

, UV: ? max (EtOH): 235, 281 nm. FTIR (neat): ? max : 1729 (C=O), p.1512

H. Nmr, (2H, m, H 8 ), 6.69 (4H, m, H, vol.3, pp.172-181

, 68.8 (C 13 ), vol.138, p.17

, Bis-Decene-O-Dihydroferuloyl, vol.1, p.4

, Colorless oil (82%). UV: ? max (EtOH): 228, 281 nm. FTIR (neat): ? max : 1732 (C=O), 1512 (C=C Ar). 1 H NMR (300 MHz, vol.3, p.33

. Bis-allyl-o-dihydroferuloyl-isosorbide,

, White powder (60%) UV: ? max (EtOH): 205, 228, 281 nm. FTIR (neat): ? max : 1719 (C=O), 1513 (C=C Ar) cm-1. 1 H NMR (300 MHz, vol.3, p.9

-. Bis-hexene and . Isosorbide,

, Viscous oil (78%) UV: ? max (EtOH): 202, 205, 228, 281 nm. FTIR (neat): ? max : 1736 (C=O), 1511 (C=C Ar) cm-1. 1 H NMR (300 MHz, vol.3, pp.5-77

C. Okkerse, H. Van-bekkum, and ;. D. Klass, 19' ), 113.1 (C 8,8' ), 112.1 (C 5,5' ), Green Chemistry-Frontiers in Benign Chemical Synthesis and Processes, vol.18, pp.495-542, 1998.

L. Mialon, A. G. Pemba, S. A. Miller, and G. Chem, , vol.12, p.1704, 2010.

J. Palacios and C. Perez, New Polym. Mat, vol.2, p.167, 1990.

H. G. Elias and J. A. Palacios, Makromol. Chem, vol.5, p.1027, 1985.

T. Kaneko, M. Matsuaki, T. T. Hang, M. Akashi-;-b, ). Y. Tanaka et al., 13, 235; c) B. Sapich and J. Stumpe, Macromolecules 1998, 31, 1016; d), J. Polym. Sci. B Polym. Lett. Ed, vol.25, pp.673-677, 1975.

D. Wang, K. Kaneko, X. Kan, T. Jin, and . Kaneko, Pure Appl. Chem, vol.12, 2012.

H. Hatanaka, . Okawa, ;. Q. Patent, W. Zhao, and . Wu, Polymer, vol.4, p.998, 2009.

). J. Du, Y. Fang, Y. ;. Ouimet, J. Griffin, A. L. Carbone-howell et al., Zheng Polymer, Biomacromolecules, vol.19, issue.3, p.854, 2007.

M. Quentin, V. Allasia, A. Pegard, F. Allais, P. Ducrot et al., PLoS Pathog, vol.5, issue.1, 2009.

F. Allais, M. Aouhansou, A. Majira, and P. Ducrot, , 2010.

. Ducrot, Synthesis, vol.16, 1649.

M. Mouterde, A. L. Flourat, M. M. Cannet, P. Ducrot, F. Allais et al., 17, 7282; f), Eur. J. Org. Chem, vol.1, p.14780, 2011.

F. Pion, A. F. Reano, P. Ducrot, F. Allais, and . Adv, , vol.3, p.8988, 2013.

F. Pion, P. Ducrot, and F. Allais, Macromol. Chem. Phys, vol.215, p.431, 2014.

M. Z. Oulame, F. Pion, P. Ducrot, and F. , Allais Eur. Polym. J, 2014.

H. Mutlu, L. M. De-espinosa, and M. A. Meier, Chem. Soc. Rev, vol.40, p.1404, 2011.

O. Kreye, T. Tóth, M. A. Meier, ;. Mutlu, M. A. Meier-;-l et al., 47, 1804; b), J. Polym. Sci. Part A: Polym. Chem, vol.210, 2009.

K. B. Wagener-;-e, ). O. Türünç, L. M. De-espinosa, M. A. Meier, ;. S. Günther et al., Macromol. Rapid. Commun, vol.176, issue.1, p.15, 1357.

M. Firdaus and M. A. Meier, Eur. Polym. J, vol.49, p.156, 2013.

T. Carde and D. /. , GO-102001-1461; New Continuous Isosorbide Production From Sorbitol: Office of Industrial Technologies (OIT) Agriculture Project Fact Sheet, 2012.

J. Adelman, L. F. Charbonneau, S. Ung-;-b, ). H. Yim, R. Haselbeck et al., US Patent 6, USA 15. a) S. Kobayashi, Macromol. Rapid. Commun, vol.656, 2003.

S. Schauhoff and W. Schmidt, Chem. Fibers Int, vol.46, 1996.

M. D. Watson and K. B. Wagener, Macromolecules, vol.33, p.8963, 2000.

M. D. Schulz, K. B. Wagener, . Acs-macro, and . Lett, , vol.1, p.449, 2012.

S. H. Hong, D. P. Sanders, C. W. Lee, and R. H. Grubb, J. Am. Chem. Soc, vol.31, p.368, 2005.

M. Abbas and C. Slugovc, Tetrahedron Lett, vol.52, p.2560, 2011.

U. Gaur and B. Wunderlich, Macromolecules, vol.13, p.445, 1980.