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·1296·                            精细化工   FINE CHEMICALS                                 第 38 卷

                 Synthesis and pyrolysis of 2-L-aspartic  acid-2-deoxy-D-glucose[J].   acrylamide  and furan concentrations, antioxidant activities, and
                 Food Science (食品科学), 2018, 39(5): 99-105.         volatile profiles in  cold or  hot  brew coffees[J]. Food  Science and
            [10]  ZHANG G H (张改红), BAI B (白冰), XU G G (徐改改),  et al.   Biotechnology, 2020, 29(1): 141-148.
                 Synthesis and pyrolysis of 5-methyl furfuryl alcohol-β-D-   [19]  YIN C M, FAN X Z, FAN Z, et al. Comparison of non-volatile and
                 glucopyranoside[J]. Fine Chemicals ( 精 细化工 ), 2019, 36(2):   volatile flavor compounds in six Pleurotus mushrooms[J]. Journal of
                 271-276.                                          the Science of Food and Agriculture, 2019, 99(4): 1691-1699.
            [11]  ZENG S T, SUN  S H, LIU S,  et al. Synthesis  of  α-ionyl-β-D-   [20]  KABRO A, ESCUDERO-ADAN E C, GRUSHIN V V,  et al.
                 glucoside and its property of flavor release[J]. Journal of Thermal   Biomass conversion to high value chemicals: From furfural to chiral
                 Analysis and Calorimetry, 2014, 115(2): 1049-1056.   hydrofuroins in two steps[J]. Organic Letters, 2012, 14(15): 4014-4017.
            [12]  HEHRE E J, BREWER C F, UCHIYAMA T,  et al. Scope and   [21]  HAN G Q, LIU X W,  SUN Y  J. Photocatalytic  pinacol  C—C
                 mechanism of carbohydrase action. Stereospecific hydration of   coupling and jet fuel precursor production on ZnIn 2S 4 nanosheets[J].
                 2,6-anhydro-l-deoxy-D-gluco-hept-l-enitol catalyzed by  α- and   ACS Catalysis, 2020, 10(16): 9346-9355.
                 β-glucosidases and an inverting exo-α-glucanase[J]. Biochemistry,   [22]  SHANG X, YANG  Y, SUN Y J. Electrohydrodimerization  of
                 1980, 19(15): 3557-3564.                          biomass-derived furfural generates a  jet fuel precursor[J].  Green
            [13]  KLEIN H W, IM M J, PALM D. Mechanism of the phosphorylase   Chemistry, 2020, 22(16): 5395-5401.
                 reaction[J]. European Journal of Biochemistry, 1986, 157(1):   [23]  CHADDERDON X H, CHADDERDON D J, MATTHIESEN J E, et
                 107-114.                                          al. Mechanisms  of furfural reduction on metal electrodes:
            [14]  ZHU J S, STIERS K M, WINTER S M,  et al. Synthesis,   Distinguishing pathways for selective hydrogenation of bioderived
                 derivatization, and structural analysis of phosphorylated mono-, di-,   oxygenates[J]. Journal of the American Chemical Society, 2017,
                 and trifluorinated D-gluco-heptuloses by glucokinase:  Tunable   139(40): 14120-14128.
                 phosphoglucomutase inhibition[J].  ACS  Omega, 2019, 4(4):   [24]  MAYES H B, NOLTE M W, BECHHAM G T, et al. The alpha-bet(a)
                 7029-7037.                                        of salty glucose pyrolysis: Computational investigations reveal
            [15]  ZHANG W J (张文娟), HUANG R B (黄瑞彬), XU X J (徐秀娟), et   carbohydrate pyrolysis catalytic action by sodium ions[J]. ACS
                 al. Analysis of the differences of volatile components in Xinjiang   Catalysis, 2015, 5(1): 192-202.
                 raisins[J]. Food Research  and Development (食品研究与开发),   [25]  WANG M, LIU C, XU X X, et al. Theoretical investigation on the
                 2016, 37(3): 4-9.                                 carbon sources and orientations of the aldehyde group of furfural in
            [16]  MONDELLO  L,  COSTA R, TRANCHIDA P Q,  et al. Reliable   the pyrolysis of glucose[J]. Journal of Analytical and Applied
                 characterization of coffee bean aroma profiles  by automated   Pyrolysis, 2016, 120: 464-473.
                 headspace solid phase  microextraction-gas chromatography-mass   [26]  HU B, LU Q, JIANG X Y, et al. Pyrolysis mechanism of glucose and
                 spectrometry with the support of a dual-filter mass spectra library[J].   mannose: The formation of 5-hydroxymethyl furfural and furfural[J].
                 Journal of Separation Science, 2005, 28(9/10): 1101-1109.   Journal of Energy Chemistry, 2018, 27(2): 486-501.
            [17]  WANG X J, GUO M Y, SONG H L, et al. Characterization of key   [27]  ARARA J S, ANSARI K B, CHEW J W,  et al. Unravelling  the
                 aroma compounds in traditional Chinese soy sauce through the   catalytic influence of naturally occurring salts on biomass pyrolysis
                 molecular sensory science technique[J]. LWT-Food Science and   chemistry using glucose as a  model compound: A  combined
                 Technology, 2020, 128: 109413.                    experimental and DFT study[J]. Catalysis Science & Technology,
            [18]  KANG D E, LEE H U, DAVAATSEREN M, et al. Comparison of   2019, 9(13): 3504-3524.


            (上接第 1290 页)                                       [6]   XIA R, SUN  L P, QU G  R. The synthesis of  nebularine and its
                                                                   analogs  via  oxidative desulfuration in aqueous nitric acid[J].

            参考文献:                                                  Phosphorus Sulfur and Silicon and the Related Elements, 2017,
                                                                   192(1): 88-91.
                                                               [7]   XIA R, XIE M S, NIU H Y, et al. Efficient synthesis of nebularine
            [1]   IWAMURA H, HASHIZUME T. Synthesis in nucleoside antibiotics.   and vidarabine via dehydrazination of (hetero)aromatics catalyzed by
                 Ⅱ. Facile synthesis of nebularine and its analogs by a  modified   CuSO 4 in water[J]. Green Chemistry, 2014, 16(3): 1077-1081.
                 fusion procedure[J]. Journal of Organic Chemistry, 1968, 33(5):   [8]   XIA R (夏然), SUN L P (孙莉萍), QU G R (渠桂荣). Efficient
                 1796-1799.                                        synthesis of 2,6-dichloropurine riboside from cheap inosine[J]. Fine
            [2]   SWAYZE E E, DRACH J C,  WOTRING  L  L,  et al.  Synthesis,   Chemicals (精细化工), 2016, 33(3): 339-345.
                 antiproliferative and antiviral activity  of imida-zo[4,5-d]isothiazole   [9]   JI Y F (冀亚飞), XU X (许煦). Simple synthesis of adenosine from
                 nucleosides as 5∶5 fused analogs of nebularine and 6-methylpurine   inosine[J]. Chinese Journal of Applied Chemistry (应用化学), 2007,
                 ribonucleoside[J]. Journal of Medicinal Chemistry, 1997, 40(5):   24(8): 971-973.
                 771-784.                                      [10]  WEINRICH  T, JAUMANN E A, SCHEFFER  U  M,  et al.
            [3]   XIA R, XIE M S, NIU H Y, et al. Radical route for the alkylation of   Phosphoramidite building blocks with protected nitroxides for the
                 purine nucleosides  at C6  via  Minisci reaction[J]. Organic Letters,   synthesis of spin-labeled DNA and RNA[J]. Beilstein  Journal  of
                 2014, 16(2): 444-447.                             Organic Chemistry, 2018, 14: 1563-1569.
            [4]   BUFFEL D K, MCGUIGAN C, ROBINS M J. Nucleic acid related   [11]  KONIARCZYK J  L, HESK D,  OVERGARD A,  et al. A  general
                 compounds. 48. Photoaddition of methanol to 9-(.beta.-D-   strategy for site-selective incorporation of deuterium and tritium into
                 ribofuranosyl) purine (nebularine) to  give inhibitors of  adenosine   pyridines, diazines and pharmaceuticals[J]. Journal of the American
                 deaminase[J]. Journal of Organic Chemistry, 1985, 50  (15): 2664-   Chemical Society, 2018, 140(6): 1990-1993.
                 2667.                                         [12]  HILTON M C,  DOLEWSKI  R  D, MCNALLY A. Selective
            [5]   FRANCOM P, JANEBA Z, SHIBUYA S, et al. Nucleic acid related   functionalization of pyridines via heterocyclic phosphonium salts[J].
                 compounds. 116. Nonaqueous diazotization of aminopurine   Journal  of  the  American Chemical Society, 2016, 138(42):
                 nucleosides. Mechanistic considerations and efficient procedures   13806-13809.
                 with  tert-butyl nitrite or sodium nitrite[J]. Journal of Organic   [13]  MULLARD A. Deuterated drugs draw heavier backing[J]. Nature
                 Chemistry, 2012, 67(19): 6788-6796.               Reviews Drug Discovery, 2016, 15: 219-221.
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