Tài liệu tham khảo |
Loại |
Chi tiết |
[1] R. J. Pounder, M. J. Stanford, P. Brooks, S. P. Richards, and A. P. Dove, "Metal free thiol-maleimide 'Click' reaction as a mild functionalisation strategy for degradable polymers," Chemical Communications, pp. 5158-5160, 2008 |
Sách, tạp chí |
Tiêu đề: |
Metal free thiol-maleimide 'Click' reaction as a mild functionalisation strategy for degradable polymers |
|
[2] L. Billiet, O. Gok, A. P. Dove, A. Sanyal, L.-T. T. Nguyen, and F. E. Du Prez, "Metal-Free Functionalization of Linear Polyurethanes by Thiol-Maleimide Coupling Reactions," Macromolecules, vol. 44, pp. 7874-7878, 2011/10/25 2011 |
Sách, tạp chí |
Tiêu đề: |
Metal-Free Functionalization of Linear Polyurethanes by Thiol-Maleimide Coupling Reactions |
|
[3] C. M. Nimmo and M. S. Shoichet, "Regenerative Biomaterials that “Click”: Simple, Aqueous-Based Protocols for Hydrogel Synthesis, Surface Immobilization, and 3D Patterning," Bioconjugate Chemistry, vol. 22, pp. 2199- 2209, 2011/11/16 2011 |
Sách, tạp chí |
Tiêu đề: |
Regenerative Biomaterials that “Click”: Simple, Aqueous-Based Protocols for Hydrogel Synthesis, Surface Immobilization, and 3D Patterning |
|
[4] W. Xi, C. Wang, C. J. Kloxin, and C. N. Bowman, "Nitrogen-Centered Nucleophile Catalyzed Thiol-Vinylsulfone Addition, Another Thiol-ene “Click”Reaction," ACS Macro Letters, vol. 1, pp. 811-814, 2012/07/17 2012 |
Sách, tạp chí |
Tiêu đề: |
Nitrogen-Centered Nucleophile Catalyzed Thiol-Vinylsulfone Addition, Another Thiol-ene “Click” Reaction |
|
[5] B. H. Northrop, S. H. Frayne, and U. Choudhary, "Thiol-maleimide "click" chemistry: evaluating the influence of solvent, initiator, and thiol on the reaction mechanism, kinetics, and selectivity," Polymer Chemistry, vol. 6, pp. 3415-3430, 2015 |
Sách, tạp chí |
Tiêu đề: |
Thiol-maleimide "click" chemistry: evaluating the influence of solvent, initiator, and thiol on the reaction mechanism, kinetics, and selectivity |
|
[6] L.-T. T. Nguyen, M. T. Gokmen, and F. E. Du Prez, "Kinetic comparison of 13 homogeneous thiol-X reactions," Polymer Chemistry, vol. 4, pp. 5527-5536, 2013 |
Sách, tạp chí |
Tiêu đề: |
Kinetic comparison of 13 homogeneous thiol-X reactions |
|
[7] C. E. Hoyle, A. B. Lowe, and C. N. Bowman, "Thiol-click chemistry: a multifaceted toolbox for small molecule and polymer synthesis," Chemical Society Reviews, vol. 39, pp. 1355-1387, 2010 |
Sách, tạp chí |
Tiêu đề: |
Thiol-click chemistry: a multifaceted toolbox for small molecule and polymer synthesis |
|
[8] A. B. Lowe and M. A. Harvison, "Thiol-Based ‘Click’ Chemistries in Polymer Synthesis and Modification," Australian Journal of Chemistry, vol. 63, pp. 1251- 1266, 2010 |
Sách, tạp chí |
Tiêu đề: |
Thiol-Based ‘Click’ Chemistries in Polymer Synthesis and Modification |
|
[9] H. C. Kolb, M. G. Finn, and K. B. Sharpless, "Click Chemistry: Diverse Chemical Function from a Few Good Reactions," Angewandte Chemie International Edition, vol. 40, pp. 2004-2021, 2001 |
Sách, tạp chí |
Tiêu đề: |
Click Chemistry: Diverse Chemical Function from a Few Good Reactions |
|
[10] B. D. Mather, K. Viswanathan, K. M. Miller, and T. E. Long, "Michael addition reactions in macromolecular design for emerging technologies," Progress in Polymer Science, vol. 31, pp. 487-531, 2006 |
Sách, tạp chí |
Tiêu đề: |
Michael addition reactions in macromolecular design for emerging technologies |
|
[12] C. F. Nising and S. Brase, "The oxa-Michael reaction: from recent developments to applications in natural product synthesis," Chemical Society Reviews, vol. 37, pp. 1218-1228, 2008 |
Sách, tạp chí |
Tiêu đề: |
The oxa-Michael reaction: from recent developments to applications in natural product synthesis |
|
[13] A. B. Lowe, "Thiol-ene "click" reactions and recent applications in polymer and materials synthesis," Polymer Chemistry, vol. 1, pp. 17-36, 2010 |
Sách, tạp chí |
Tiêu đề: |
Thiol-ene "click" reactions and recent applications in polymer and materials synthesis |
|
[14] C. Walling and W. Helmreich, "Reactivity and Reversibility in the Reaction of Thiyl Radicals with Olefins1," Journal of the American Chemical Society, vol |
Sách, tạp chí |
Tiêu đề: |
Reactivity and Reversibility in the Reaction of Thiyl Radicals with Olefins1 |
|
[15] D. P. Nair, M. Podgórski, S. Chatani, T. Gong, W. Xi, C. R. Fenoli, et al., "The Thiol-Michael Addition Click Reaction: A Powerful and Widely Used Tool in Materials Chemistry," Chemistry of Materials, vol. 26, pp. 724-744, 2014/01/14 2014 |
Sách, tạp chí |
Tiêu đề: |
The Thiol-Michael Addition Click Reaction: A Powerful and Widely Used Tool in Materials Chemistry |
|
[16] J. E. Moses and A. D. Moorhouse, "The growing applications of click chemistry," Chemical Society Reviews, vol. 36, pp. 1249-1262, 2007 |
Sách, tạp chí |
Tiêu đề: |
The growing applications of click chemistry |
|
[17] A. B. Lowe, "Thiol-ene "click" reactions and recent applications in polymer and materials synthesis: a first update," Polymer Chemistry, vol. 5, pp. 4820-4870, 2014 |
Sách, tạp chí |
Tiêu đề: |
Thiol-ene "click" reactions and recent applications in polymer and materials synthesis: a first update |
|
[18] C. E. Hoyle, T. Y. Lee, and T. Roper, "Thiol–enes: Chemistry of the past with promise for the future," Journal of Polymer Science Part A: Polymer Chemistry, vol. 42, pp. 5301-5338, 2004 |
Sách, tạp chí |
Tiêu đề: |
Thiol–enes: Chemistry of the past with promise for the future |
|
[19] C. E. Hoyle and C. N. Bowman, "Thiol–Ene Click Chemistry," Angewandte Chemie International Edition, vol. 49, pp. 1540-1573, 2010 |
Sách, tạp chí |
Tiêu đề: |
Thiol–Ene Click Chemistry |
|
[20] M. J. Kade, D. J. Burke, and C. J. Hawker, "The power of thiol-ene chemistry," Journal of Polymer Science Part A: Polymer Chemistry, vol. 48, pp. 743-750, 2010 |
Sách, tạp chí |
Tiêu đề: |
The power of thiol-ene chemistry |
|
[21] J. W. Chan, C. E. Hoyle, A. B. Lowe, and M. Bowman, "Nucleophile-Initiated Thiol-Michael Reactions: Effect of Organocatalyst, Thiol, and Ene,"Macromolecules, vol. 43, pp. 6381-6388, 2010/08/10 2010 |
Sách, tạp chí |
Tiêu đề: |
Nucleophile-Initiated Thiol-Michael Reactions: Effect of Organocatalyst, Thiol, and Ene |
|