Page 95 - 《精细化工》2020年第8期
P. 95

第 8 期                      张田田,等:  醇的种类对球形 γ-Al 2 O 3 多孔结构的影响                           ·1593·


                 Materials, 2004, 14(4): 309-322.              [23]  MORTERRA  C,  MAGNACCA  G,  MAESTRIT  P  P  D.  Surface
            [15]  VINOGRADOV  V  V,  VINOGRADOV  A  V,  KRAEV  A  S,  et al.   characterization of modified aluminas[J]. Journal of Catalysis, 1995,
                 Sol-gel synthesis, characterization and catalytic activity of γ-alumina   152: 384-395.
                 with  bimodal  mesopore  distribution[J].  Journal  of  Sol-Gel  Science   [24]  WANG  J,  WANG  Y  H,  WEN  J  W,  et al.  Effect  of  phosphorus
                 and Technology, 2013, 68(2): 155-161.             introduction strategy on the surface texture and structure of modified
            [16]  ARSIA A T, SERGE K. Synthesis of ordered mesoporous γ-alumina   alumina[J]. Microporous and Mesoporous Materials, 2009, 121(1/2/3):
                 effects of calcination conditions and polymeric template concentration   208-218.
                 [J]. Microporous and Mesoporous Materials, 2017, 248: 179-191.   [25]  FEDOROV  A  V,  GULYAEVA  Y  K.  Strength  statistics  for  porous
            [17]  CABRERA S, HASKOURI J E, ALAMO J, et al. Surfactant assisted   alumina [J]. Powder Technology, 2019, 343: 783-791.
                 synthesis  of  mesoporous  alumina  showing  continuously  adjustable   [26]  DILSIZ N, AKOVAH G. Study of sol-gel processing for fabrication
                 pore sizes[J]. Advanced Materials, 1999, 11(5): 379-381.   of  low  density  alumina  microspheres[J].  Materials  Science  and
            [18]  CEJKA J. Organized mesoporous alumina: Synthesis, structure and   Engineering A, 2002, 332: 91-96.
                 potential in catalysis[J]. Applied Catalysis A: General, 2003, 254(2):   [27]  MENG G Y, YU H B, SUN Y M, et al. Method for preparing spherical
                 327-338.                                          alumina: CN106745125A[P]. 2017-05-31.
            [19]  XU  B  J,  XIAO  T  C,  YAN  Z  F,  et al.  Synthesis  of  mesoporous   [28]  LYU  Z  H,  PENG  S  Z,  ZHANG  X  H,  et al.  Method  for  preparing
                 alumina  with  highly  thermal  stability  using  glucose  template  in   spherical modified alumina carrier: CN106669853A[P]. 2017-05-17.
                 aqueous  system[J].  Microporous  and  Mesoporous  Materials,  2006,   [29]  LIU  J  L,  PAN  J  C,  WANG  G  C.  Method  for  preparing  spherical
                 91(1): 293-295.                                   alumina using oil ammonia column: CN103011213A[P]. 2013-04-03.
            [20]  YIN F S (殷福珊), YAO Z X (姚振兴), ZHU X R (朱锡如). Preparation   [30]  LIU J L, PAN J C, MA A J, et al. Method for preparing spherical
                 of macroporous γ-alumina pellets[J]. Petrochemical Technology (石  alumina: CN104418371A[P]. 2015-03-18.
                 油化工), 1982, 1(11): 7-13.                      [31]  YU H B, YANG W J, MENG G Y, et al. Method for preparing large
            [21]  SHANG  L  D  (商连弟),  WANG  H  H  (王惠惠).  Production  and   pore volume spherical alumina: CN104353502A[P]. 2015-02-18.
                 modification  of  activated  alumina[J].  Inorganic  Chemicals  Industry   [32]  WANG  G  C,  PAN  J  C,  MA  A  Z.  Spherical  alumina  oil  ammonia
                 (无机盐工业), 2012, 44(1): 1-6.                        column forming method: CN1493524A[P]. 2004-05-05.
            [22]  MEKHEMER  G  A  H,  NOHMAN  A  K  H,  FOUAD  N  E,  et al.   [33]  SZETU J L, FROST R L, KLOPROGGE J T, et al. Dehydration and
                 Surface to bulk characterization of phosphate modified aluminas[J].   dehydroxylation of alumina gels prepared from tri-sec-butoxyaluminium
                 Colloids and Surfaces A: Physicochemical and Engineering Aspects,   modified  with  short  chain  aliphatic  acids[J].  Thermochimica  Acta,
                 2000, 161(3): 439-446.                            2000, 362(1/2): 37-48.


            (上接第 1532 页)                                           condensation/azide-alkyne 1,3-dipolar cycloaddition reaction in one
                                                                   pot[J]. ACS Combinatorial Science, 2014, 16: 466-477.
            [39]  XIAO T B, PENG P, ZHOU L, et al. Ag(Ⅰ)-catalyzed three-component   [46]  ENOMOTO  T,  GIRARD  A  L,  TAKEMOTO  Y,  et al.  Gold(Ⅰ)-
                 reaction  of  2-alkynylbenzaldehydes,  amines,  and  diazo  compounds   catalyzed  tandem  reactions  initiated  by  hydroamination  of  alkynyl
                 [J]. Organic Letters, 2015, 17: 4332-4335.        carbamates:  Application  to  the  synthesis  of  nitidine[J].  Journal  of
            [40]  PAL  M,  RAO  A  S,  RAO  V  M,  et al.  Ultrasound  assisted  Cu-   Organic Chemistry. 2009, 74(23): 9158-9159.
                 catalyzed  synthesis  of 1,2-disubstituted  benzimidazoles  as  potential   [47]  HSU Y C, TING C M, LIU R S, et al. Stereocontrolled synthesis of
                 antibacterial agents[J]. Mini Reviews in Medicinal Chemistry, 2018,   complicated  oxacyclic  compounds  via  platinum-catalyzed  [4+2]-
                 18(14): 1233-1239.                                cycloadditions  and  annulations  of  enynals  with  allylic  alcohols[J].
            [41]  OUYANG  H  C,  ZHONG  P,  ZHANG  X  G,  et al.  CuI/I 2-promoted   Journal of the American Chemistry Society, 2009, 131(6): 2090- 2091.
                 electrophilic  tandem  cyclization  of  2-ethynylbenzaldehydes  with   [48]  XIAO  Q,  YE  S  Q,  WU  J.  Silver(Ⅰ)-catalyzed  tandem  reaction  of
                 ortho-  benzenediamines:  Synthesis  of  iodoisoquinoline-fused   2-alkynylbenzaldoxime  with  alkylidenecyclopropane[J].  Organic
                 benzimidazoles  [J].  Journal  of  Organic  Chemistry,  2011,  76(1):   Letters, 2012, 14(13): 3430-3433.
                 223-228.                                      [49]  QIAO  J,  LIU  B,  LIAO  Z,  et al.  One-pot  to  fused  pyrazoles  by  a
            [42]  DING C F, ZHANG R P, YU H F, et al. Hybrid isoquinolines from   double cyclization of o-alkynylaldehydes with ketones and hydrazine
                 Thalictrum foetidum: A new type of aporphine inhibiting staphylococcus   under metal-free condition[J]. Tetrahedron, 2014, 70(24), 3782-3787.
                 aureus  by  combined  mechanisms[J].  Organic  Chemistry  Frontiers,   [50]  ZHOU  P,  HAO  W  J,  TU  S  J,  et al.  Cascade  bicyclizations  of
                 2019, 6(19): 3428-3434.                           o-alkynyl aldehydes with thiazolium salt: A new access toward poly-
            [43]  VERMA  A  K,  CHOUDHARY  D,  SAUNTHWAL  R  K,  et al.  On   functionalized indeno[2,1-b] pyrroles[J]. Chemical Communications,
                 water:  Silver-catalyzed  domino  approach  for  the  synthesis  of   2015, 51(65): 13012-13015.
                 benzoxazine/oxazine-fused  isoquinolines  and  naphthyridines  from   [51]  FENG B B, LIU J Q, WANG X S. Cu(OAc) 2-catalyzed aerobic oxidative
                 o-alkynyl  aldehydes[J].  Journal  of  Organic  Chemistry,  2013,  78:   dehydrogenation  coupling:  Synthesis  of  heptacyclic  quinolizino
                 6657-6669.                                        [3,4,5,6-kla]perimidines[J]. Journal of Organic Chemistry, 2017, 82:
            [44]  KRASNIQI  B,  DEHAEN  W.  Synthesis  of  1,2,3-triazolo-fused   1817-1822.
                 allocolchicine  analogs  via  intramolecular  oxidative  biaryl  coupling   [52]  MAO X F, ZHU X P, LIU P N, et al. Cu-catalyzed cascade annulation
                 [J]. Organic Letters, 2019, 21(13): 5002-5005.     of  alkynols  with  2-azidobenzaldehydes:  Access  to  6H-isochromeno
            [45]  MAURYA R A, ADIYALA P R, KAMAL A, et al. Rapid access to   [4,3-c] quinoline[J]. Journal of Organic Chemistry, 2017, 82: 7032-
                 novel  1,2,3-triazolo-heterocyclic  scaffolds  via  tandem  knoevenagel   7039.
   90   91   92   93   94   95   96   97   98   99   100