• 综述 •
冯云超, 左淼, 曾宪海*, 孙勇, 唐兴, 林鹿*. 葡萄糖制备5-羟甲基糠醛[J]. 化学进展, 2018, 30(2/3): 314-324.
Yunchao Feng, Miao Zuo, Xianhai Zeng*, Yong Sun, Xing Tang, Lu Lin*. Preparation of 5-Hydroxymethylfurfural from Glucose[J]. Progress in Chemistry, 2018, 30(2/3): 314-324.
中图分类号:
分享此文:
[1] Corma A, Iborra S, Velty A. Chem. Rev., 2007, 107(6):2411. [2] Huber G W, Iborra S, Corma A. Chem. Rev., 2006, 106(9):4044. [3] Li C Z, Zhao X C, Wang A Q, Huber G W, Zhang T. Chem. Rev., 2015, 115(21):11559. [4] Alonso D M, Bond J Q, Dumesic J A. Green Chem., 2010, 12(9):1493. [5] Wang J J, Xi J X, Wang Y Q. Green Chem., 2015, 17(2):737. [6] Kiermayer J. Chem. Ztg, 1895, 19:1003. [7] Düll G. Chem. Ztg, 1895, 19:216. [8] Van Enenstein W, Blanksma J. Chem. Weeklad, 1909, 6:717. [9] Mascal M, Nikitin E B. Angew. Chem. Int. Ed., 2008, 47(41):7924. [10] De S, Dutta S, Saha B. ChemSusChem, 2012, 5(9):1826. [11] Roman-Leshkov Y, Barrett C J, Liu Z Y, Dumesic J A. Nature, 2007, 447(7147):982. [12] Rosatella A A, Simeonov S P, Frade R F, Afonso C A. Green Chem., 2011, 13(4):754. [13] Ståhlberg T, Fu W J, Woodley J M, Riisager A. ChemSusChem, 2011, 4(4):451. [14] Wang H L, Kong Q Q, Wang Y X, Deng T S, Chen C M, Hou X L, Zhu Y L. ChemCatChem, 2014, 6(3):728. [15] Hu Z, Liu B, Zhang Z H, Chen L Q. Ind. Crops Prod., 2013, 50:264. [16] Yang Y, Hu C W, Abu-Omar M M. Green Chem., 2012, 14(2):509. [17] Choudhary V, Mushrif S H, Ho C, Anderko A, Nikolakis V, Marinkovic N S, Frenkel A I, Sandler S I, Vlachos D G. J. Am. Chem. Soc., 2013, 135(10):3997. [18] Loerbroks C, van Rijn J, Ruby M P, Tong Q, Schüth F, Thiel W. Chem. -Eur. J., 2014, 20(38):12298. [19] Bhaumik P, Dhepe P L. Catal. Rev., 2016, 58(1):36. [20] Yang Y, Hu C W, Abu-Omar M M. J. Mol. Catal. A:Chem., 2013, 376:98. [21] Sarwono A, Man Z, Muhammad N, Khan A S, Hamzah W S W, Rahim A H A, Ullah Z, Wilfred C D. Ultrason. Sonochem., 2017, 37:310. [22] Aida T M, Sato Y, Watanabe M, Tajima K, Nonaka T, Hattori H, Arai K. J. Supercrit. Fluids, 2007, 40(3):381. [23] Qi X H, Watanabe M, Aida T M, Smith R L. Catal. Commun., 2008, 9(13):2244. [24] Qi J, Lv X Y. Chin. J. Chem. Eng., 2008, 16(6):890. [25] Cole-Hamilton D J. Science, 2003, 299(5613):1702. [26] Li M H, Li W Z, Lu Y J, Jameel H, Chang H M, Ma L L. RSC Adv., 2017, 7(24):14330. [27] Pagan-Torres Y J, Wang T F, Gallo J M R, Shanks B H, Dumesic J A. ACS Catal., 2012, 2(6):930. [28] Eminov S, Brandt A, Wilton-Ely J D, Hallett J P. PLoS One, 2016, 11(10):e0163835. [29] Teng J J, Ma H, Wang F R, Wang L F, Li X H. Bioresources, 2016, 11(1):2152. [30] Xu Z L, Wang X Y, Shen M Y, Du C H. Chem. Pap., 2016, 70(12):1649. [31] Zhou J X, Xia Z, Huang T Y, Yan P F, Xu W J, Xu Z W, Wang J J, Zhang Z C. Green Chem., 2015, 17(8):4206. [32] Li J J, Ma Y B, Wang L, Song Z, Li H P, Wang T F, Li H Y, Eli W. Catalysts, 2015, 6(1):1. [33] Di Serio M, Tesser R, Lu P M, Santacesaria E. Energy Fuels, 2007, 22(1):207. [34] Nasirudeen M B, Hailes H C, Evans J R G. Curr. Org. Synth., 2017, 14(4):596. [35] Yan H P, Yang Y, Tong D M, Xiang X, Hu C W. Catal. Commun., 2009, 10(11):1558. [36] 于世涛(Yu S T), 刘福胜(Liu F S). 固体酸与精细化工(Solid Acid and Fine Chemical Industry), 北京:化学工业出版社(Beijing:Chemical Industry Press), 2006. 23. [37] Wang Y P, Liu Y H, Yang L, Ruan R, Wen P W, Wan Y Q. Synth. React. Inorg. Met.-Org. Chem., 2016, 46(2):177. [38] García-Sancho C, Fúnez-Núñez I, Moreno-Tost R, Santamaría-González J, Pérez-Inestrosa E, Fierro J L G, Maireles-Torres P. Appl. Catal. B-Environ., 2017, 206:617. [39] Jiao H F, Zhao X L, Lv C X, Wang Y J, Yang D J, Li Z H, Yao X D. Sci. Rep., 2016, 6. [40] Martínez J J, Silva D F, Aguilera E X, Rojas H A, Brijaldo M H, Passos F B, Romanelli G P. Catal. Lett., 2017, 147(7):1765. [41] Guo J, Zhu S H, Cen Y L, Qin Z F, Wang J G, Fan W B. Appl. Catal. B-Environ., 2017, 200:611. [42] Yue C C, Li G N, Pidko E A, Wiesfeld J J, Rigutto M, Hensen E J. ChemSusChem, 2016, 9(17):2421. [43] Su Y, Chang G G, Zhang Z G, Xing H B, Su B G, Yang Q W, Ren Q L, Yang Y W, Bao Z B. AIChE J., 2016, 62(12):4403. [44] Yabushita M, Li P, Islamoglu T, Kobayashi H, Fukuoka A, Farha O K, Katz A. Ind. Eng. Chem. Res., 2017, 56(25):7141. [45] Chen D W, Liang F B, Feng D X, Xian M, Zhang H B, Liu H Z, Du F L. Chem. Eng. J., 2016, 300:177. [46] Li W Z, Zhang T W, Xin H S, Su M X, Ma L L, Jameel H, Chang H M, Pei G. RSC Adv., 2017, 7(44):27682. [47] Thombal R S, Jadhav V H. Appl. Catal., A, 2015, 499:213. [48] Jiménez-Morales I, Santamaría-González J, Jiménez-López A, Maireles-Torres P. Fuel, 2014, 118:265. [49] Jiménez-Morales I, Moreno-Recio M, Santamaría-González J, Maireles-Torres P, Jimenez-Lopez A. Appl. Catal. B-Environ., 2015, 164:70. [50] Xu Q, Zhu Z, Tian Y K, Deng J, Shi J, Fu Y. Bioresources, 2013, 9(1):303. [51] Moreno-Recio M, Santamaría-González J, Maireles-Torres P. Chem. Eng. J., 2016, 303:22. [52] Wang P, Ren L H, Lu Q Y, Huang Y B. Chem. Eng. Commun., 2016, 203(11):1507. [53] Liu H, Wang H W, Li Y, Yang W, Song C H, Li H M, Zhu W S, Jiang W. RSC Adv., 2015, 5(12):9290. [54] Ravasco J M J M, Coelho J A S, Simeonov S P, Afonso C A M. RSC Adv., 2017, 7(13):7555. [55] Lu Y M, Li H, He J, Liu Y X, Wu Z B, Hu D Y, Yang S. RSC Adv., 2016, 6(16):12782. [56] Liu B, Ba C, Jin M M, Zhang Z H. Ind. Crops Prod., 2015, 76:781. [57] Wang J J, Ren J W, Liu X H, Xi J X, Xia Q N, Zu Y H, Lu G Z, Wang Y Q. Green Chem., 2012, 14(9):2506. [58] Guo X Q, Zhu C H, Guo F. Bioresources, 2016, 11(1):2457. [59] Gascon J, Corma A, Kapteijn F, Llabrés i Xamena F X. ACS Catal., 2013, 4(2):361. [60] Lee J, Farha O K, Roberts J, Scheidt K A, Nguyen S T, Hupp J T. Chem. Soc. Rev., 2009, 38(5):1450. [61] Valvekens P, Vermoortele F, De Vos D. Catal. Sci. Technol., 2013, 3(6):1435. [62] Herbst A, Janiak C. New J. Chem., 2016, 40(9):7958. [63] Mondloch J E, Bury W, Fairen-Jimenez D, Kwon S, DeMarco E J, Weston M H, Sarjeant A A, Nguyen S T, Stair P C, Snurr R Q, Farha O K, Hupp J T. J. Am. Chem. Soc., 2013, 135(28):10294. [64] Kruse A, Dinjus E. J. Supercrit. Fluids, 2007, 39(3):362. [65] Shuai L, Luterbacher J. ChemSusChem, 2016, 9(2):133. [66] Kimura H, Nakahara M, Matubayasi N. J. Phys. Chem. A, 2011, 115(48):14013. [67] Vasudevan V, Mushrif S H. RSC Adv., 2015, 5(27):20756. [68] Sun J K, Yuan X D, Shen Y, Yi Y X, Wang B, Xu F, Sun R C. Ind. Crops Prod., 2015, 70:266. [69] Girisuta B, Janssen L P B M, Heeres H J. Chem. Eng. Res. Des., 2006, 84(5):339. [70] Gürbüz E I, Wettstein D S G, Dumesic P J A. ChemSusChem, 2012, 5(2):383. [71] Román-Leshkov Y, Dumesic J A. Top. Catal., 2009, 52(3):297. [72] Binder J B, Raines R T. J. Am. Chem. Soc., 2009, 131(5):1979. [73] Wasserscheid P, Keim W. Angew. Chem. Int. Ed., 2000, 39(21):3772. [74] Rogers R D, Seddon K R. Science, 2003, 302(5646):792. [75] 胡磊(Hu L), 孙勇(Sun Y), 林鹿(Lin L). 化学进展(Progress in Chemistry), 2012, 24(4):483. [76] Zhao H B, Holladay J E, Brown H, Zhang Z C. Science, 2007, 316(5831):1597. [77] Li C Z, Zhang Z H, Zhao Z B K. Tetrahedron Lett., 2009, 50(38):5403. [78] D'Anna F, Marullo S, Vitale P, Rizzo C, Meo P L, Noto R. Appl. Catal. A, 2014, 482(28):287. [79] Tang X, Zuo M, Li Z, Liu H, Xiong C X, Zeng X H, Sun Y, Hu L, Liu S J, Lei T Z, Lin L. ChemSusChem, 2017, 10(13):2696. [80] Paiva A, Craveiro R, Aroso I, Martins M, Reis R L, Duarte A R C. ACS Sustain Chem. Eng., 2014, 2(5):1063. [81] Matsumiya H, Hara T. Biomass Bioenerg., 2015, 72:227. [82] Zuo M, Le K, Li Z, Jiang Y T, Zeng X H, Tang X, Sun Y, Lin L. Ind. Crops Prod., 2017, 99:1. [83] Liu F, Audemar M, Vigier K D O, Cartigny D, Clacens J M, Gomes M F C, Pádua A A, De Campo F, Jérôme F. Green Chem., 2013, 15(11):3205. [84] Ilgen F, Ott D, Kralisch D, Reil C, Palmberger A, König B. Green Chem., 2009, 11(12):1948. [85] Yang J, De Oliveira Vigier K, Gu Y L, Jerome F. ChemSusChem, 2015, 8(2):269. |
[1] | 夏博文, 朱斌, 刘静, 谌春林, 张建. 电催化氧化制备2,5-呋喃二甲酸[J]. 化学进展, 2022, 34(8): 1661-1677. |
[2] | 程丽丽, 章赟, 朱烨坤, 吴瑛. 选择性氧化HMF[J]. 化学进展, 2021, 33(2): 318-330. |
[3] | 刘毅强, 裘依梅, 唐兴, 孙勇, 曾宪海, 林鹿. 化学催化葡萄糖异构化果糖[J]. 化学进展, 2021, 33(11): 2128-2137. |
[4] | 尹钰, 马春慧, 李伟, 刘守新. 葡萄糖制备5-羟甲基糠醛的溶剂体系及转化机理[J]. 化学进展, 2021, 33(10): 1856-1873. |
[5] | 刘雪晨, 邢娟娟, 王海鹏, 周沅逸, 张玲, 王文中. HMF催化合成生物基聚酯单体FDCA[J]. 化学进展, 2020, 32(9): 1294-1306. |
[6] | 孙子茹, 刘胜男, 高清志. 靶向葡萄糖转运蛋白(GLUTs)抗癌药物的开发[J]. 化学进展, 2020, 32(12): 1869-1878. |
[7] | 方莉, 贺进禄. 无酶葡萄糖传感器[J]. 化学进展, 2015, 27(5): 585-593. |
[8] | 张宇琪, 俞计成, 沈群东, 顾臻. 随葡萄糖响应的合成类闭路胰岛素递释系统[J]. 化学进展, 2015, 27(1): 11-26. |
[9] | 李京, 谢小丽, 王佳佳, 王晓敏, 李静, 王鹏. 戈谢病的药物分子伴侣[J]. 化学进展, 2014, 26(05): 889-897. |
[10] | 周理龙, 吴廷华*, 吴瑛*. 纤维素在离子液体中的降解转化[J]. 化学进展, 2012, 24(08): 1533-1543. |
[11] | 胡磊, 孙勇, 林鹿. 离子液体介导制备5-羟甲基糠醛[J]. 化学进展, 2012, 24(04): 483-491. |
[12] | 石文韬, 邸静, 马占芳. 电化学葡萄糖传感器[J]. 化学进展, 2012, 24(04): 568-576. |
[13] | 胡磊, 孙勇, 林鹿. 生物质转化为液体燃料2,5-二甲基呋喃 的途径与机理[J]. 化学进展, 2011, 23(10): 2079-2084. |
[14] | 李艳 魏作君 陈传杰 刘迎新. 碳水化合物降解为5-羟甲基糠醛的研究*[J]. 化学进展, 2010, 22(08): 1603-1609. |
[15] | 黄世勇,王富丽,潘丽霞. 果糖脱水制备5-羟甲基糠醛*[J]. 化学进展, 2009, 21(0708): 1442-1449. |
阅读次数 | ||||||
全文 |
|
|||||
摘要 |
|
|||||