Page 242 - 《精细化工》2023年第4期
P. 242

g928g                             ㇫㏳ࡃጒ   FINE CHEMICALS                                 す 40 ࢤ

                 synthesis. Recent advances[J]. Tetrahedron, 2004, 60(42): 9325-9374.   bimetal system in aqueous media[J]. Chemical Reagents (ࡃ႓䄂ݯ),
            [6]   SERGIUS R. Neue syntheses zweiatomigereinba-sischersaurenaus   2011, 33(7): 597-602.
                 den ketonen[J]. Berichte Der Deutschen Chemischen Gesellschaft,   [22]  ZHANG J M, ZHANG Y M. Sm/BiCl 3 system mediated Reformatsky
                 1887, 20(1): 1210-1211.                           type reactions of Į-bromoaceto-phenone with aldehydes in THF-H 2O
            [7]   CHOPPIN S, FERREIRO M L, BARBAROTTOA M, et al. Recent   solvent[J]. Chinese Journal of Organic Chemistry, 2002, 20(1): 111-113.
                 advances in the diastereoselective  Reformatsky-type reaction[J].   [23]  SANTANIELLO E, MANZOCCHI A. Use of the Zn-Cu couple in
                 Chemical Society Reviews, 2013, 42: 937-949.      the Reformatsky reaction[J]. Synthesis, 1977, 1977(10): 698-699.
            [8]   SHEN Z L, WANG S Y, CHOK Y K, et al. Organoindium reagents:   [24]  HUI  Y, CAO C R, JIANG M,  et al. Metal-mediated Reformatsky
                 The preparation and application in organic synthesis[J]. Chemical   reaction of bromodifluoromethyl ketone and aldehyde using water as
                 Reviews, 2013, 113(1): 271-401.                   solvent[J]. Journal of Fluorine Chemistry, 2013, 156: 45-50.
            [9]   PENG Y Y, LIU P, LIU Z J,  et al. Egio-diastereoselective   [25]  KUROBOSHI M, ISHIHARA T. An efficient and general method for
                 Reformatsky reaction of chiral fluoroalkyl  Į,ȕ-unsaturated  N-tert-   the Reformatsky-type reaction of chlorodifluoromethyl ketones with
                 butanesulfinylketimines: Efficient asymmetric synthesis of  ȕ-   carbonyl compounds giving  a,a-difluoro-ß-hydroxy ketones[J].
                 fluoroalkyl  ȕ-vinyl  ȕ-amino esters[J]. Tetrahedron, 2018, 74(24):   Bulletin of the Chemical Society of Japan, 1990, 63(2): 428-437.
                                                                                             +
                 3074-3080.                                    [26]  DAS M, MANVAR A, FOX I, et al. Bu 4N -controlled addition and
            [10]  FERNANDEZ S L, FERNANDEZ S J A, MAESTRO M C, et al.   olefination with ethyl 2-(trimethylsilyl)acetate via silicon activation[J].
                 Reformatsky reaction to alkynyl N-tert-butanesulfinyl imines: Lewis   Synlett, 2017, 28(18): 2401-2406.
                 acid controlled stereodivergent synthesis of ȕ-alkynyl-ȕ-amino acids[J].   [27]  TALWAR D, WU X F, SAIDI O, et al. Versatile iridicycle catalysts
                 The Journal of Organic Chemistry, 2018, 83(20): 12903-12910.     for highly efficient and chemoselective transfer hydrogenation of
            [11]  FERNANDEZ I M A, MACIA B, MINNAARD A J, et al. Catalytic   carbonyl compounds in water[J]. Chemistry European Journal, 2014,
                 enantioselective Reformatsky reaction with aldehydes[J]. Angewandte   20(40): 12835-12842.
                 Chemie International Edition, 2008, 47(7): 1317-1319.   [28]  OUYANG L, LIAO J H, XIA Y P, et al. Access to ȕ-hydroxyl esters
            [12]  MAESTRO  A,  MARIGORTA E M, PALACIOS F,  et al.   via copper-catalyzed Reformatsky  reaction of  ketones and
                 Enantioselective aza-Reformatsky reaction with ketimines[J]. Organic   aldehydes[J]. Synlett, 2020, 31(14): 1418-1422.
                 Letters, 2019, 21(23): 9473-9477.             [29]  ZOU X L, DU G F, SUN W F, et al. N-heterocyclic carbenemediated
            [13]  CHATTOPADHYAY A, KRDUBEY A. A simple  and efficient   Reformatsky reaction of aldehydes with  Į-trimethylsilylcarbonyl
                 procedure of low valent iron or copper-mediated Reformatsky reaction   compounds[J]. Tetrahedron, 2013, 69(2): 607-612.
                 of aldehydes[J]. The Journal of Organic Chemistry, 2007, 72(24):   [30]  REDDY K R, MATELICH M C, UGARKAR B G, et al. Pradefovir:
                 9357-9359.                                        A prodrug that targets adefovir to the liver for the treatment of
            [14]  MORIWAKE T. The Reformatsky reaction.  ē  Condensation of   hepatitis B[J]. Journal of Medicinal Chemistry, 2008, 51(3): 666-676.
                 ketones and t-butyl bromoacetate by magnesium[J]. The Journal of   [31]  SAILER M, DUBICKI K, SORENSEN J. The synthesis of medium-
                 Organic Chemistry, 1966, 31(3): 983-985.          chain-length  ȕ-hydroxy esters via  the Reformatsky reaction[J].
            [15]  LIU Y (݅ຂ). Study on Reformatsky type reaction induced by   Synthesis, 2014, 47(1): 79-82.
                 magnesium in aqueous phase[D]. Tianjing: Tianjing University, 2006.   [32]  KAZUYUKI S, ATSUSHI T, TETSUYA K, et al. Rhodium-catalyzed
            [16]  XIA Y P (฼㞠㤺), OUYANG L (⁔䭠䱟), LIAO J H  (ᐃᐧࡻ),   Reformatsky-type reaction of ethyl bromodifluoroacetate[J]. Tetrahedron
                 et al. Manganese-mediated Reformatsky reaction: Highly divergent   Letters, 2004, 45(29): 5735-5737.
                 synthesis of  ȕ-hydroxyalkanoates[J]. Chinese Journal of Organic   [33]  ALCAZARl J, HOZ A, DIAZ A,  et al. Reformatsky and blaise
                 Chemistry (ᰶᱧࡃ႓), 2021, 41(1): 341-347.           reactions in flow as a tool  for drug  discovery. One pot diversity
            [17]  CHUNG W J, HIGASHIYA S, WELCH J T. The indium-mediated   oriented synthesis of valuable intermediates and heterocycles[J].
                 Reformatsky  reactions of 2,2-difluoro-2-halo-1-furan-2-ylethanones   Green Chemistry, 2017, 19: 1420-1424.
                 in aqueous media[J]. Journal of Fluorine Chemistry, 2001, 112(2): 343-347.   [34]  PIER G C. A catalytic, Me 2Zn-mediated, enantioselective Reformatsky
            [18]  SIANST M, ZUCCOLO M, WISCHNAT J,  et al. Samarium   reaction with ketones[J]. Angewandte Chemie, 2006, 118(18): 3017-
                 iodide-promoted asymmetric Reformatsky reaction of 3-(2-haloacyl)-   3020.
                 2-oxazolidinones with enals[J]. The Journal  of Organic Chemistry,   [35]  KEUKELEIRE D D, SAEYENS W. Convenient access to 4,4- disubstituted
                 2019, 84(16): 10050-10064.                        4H-chromenes  synthesis of 4-methyl-4-(4-methoxyphenyl)-  benzo-4H-
            [19]  WANG Y J, ZHU L, SHAO Z H, et al. Unmasking the ligand effect   chromene[J]. Synthetic Communications, 1996, 26(23): 4397-4402.
                 in manganese-catalyzed hydrogenation: Mechanistic insight and   [36]  AUWERS  K  V,  RISSE  E.  Über  die  bildung  von
                 catalytic application[J]. Journal of the American  Chemical Society,   hydrindonenausungesättigten ketonen[J]. Justus Liebigs Annalen Der
                 2019, 141(43): 17337-17349.                       Chemie, 1933, 502(1): 282-299.
            [20]  ANASTAS P T,  WARNER J C.  Green chemistry: Theory and   [37]  ALMOHAYWI B, YU T T, ISKANDERG, et al. Dihydropyrrolones
                 practice[M]. New York: Oxford University Press, 1998.   as bacterial quorum sensing inhibitors[J]. Bioorganic & Medicinal
            [21]  XIE B (䅏᪹), WANG Z G (⢸ᔄ݇), FENG J S (ۜᐧ⩠),  et al.   Chemistry Letters, 2019, 29(9): 1054-1059.
                 Reformatsky reaction of carbonyl compounds mediated by Zn/Fe




            喍̷ᣒす 919 䶢喎                                        [21]  YANG J Y, XU H, ZHANG L P, et al. Lasting superhydrophobicity
                                                                   and antibacterial activity of Cu nanoparticles immobilized on the
            [18]  WANG Z  X, XU Y C,  LUI Y  Y,  et al. a novel mussel-inspired   surface of dopamine modified cotton fabrics[J]. Surface & Coatings
                 strategy toward superhydrophobic surfaces for self-driven crude oil   Technology, 2017, 309: 149-154.
                 spill cleanup[J]. Journal of Materials Chemistry A, 2015, 3(23):   [22]  XUE C  H, BAI X, JIA S T,  et al. Self-healing superhydrophobic
                 12171-12178.
            [19]  WANG J T, LIU S Y. Fabrication of water-repellent double-layered   fabrics pre-pared by one-step coating of PDMS andoctadecylamine
                 polydopamine/copper films on mesh with improved abrasion and   [J]. Scientific Reports, 2016, 6:27262.
                 corrosion resistance by solution-phase reduction for oily wastewater   [23]  LI F, DU M, ZHENG Q. Dopamine/silica nanoparticle assembled,
                 treatment[J]. Separation and Purification Technology, 2020, 233: 116005.   microscale porous structure for versatile superamphiphobic  coating
            [20]  LU Y H (䌜㞠ࡻ),CHEN Y Y (䭵Ⴔᇠ), LIN H (᳄㏏), et al. Structure   [J]. ACS Nano, 2016, 10(2): 2910-2921.
                 and thermal property of tussah silk fiber modified with nano-titanium   [24]  YAN X, ZHU  X, RUAN Y, et al. Biomimetic, dopamine-modified
                 dioxide and chitosan[J]. Journal of Donghua University (Natural   superhydrophobic  cotton fabric for oil-water separation[J].  Cellulose,
                 Science) (͉ࡻ๔႓႓្:  㜗♣⻾႓❵), 2009, 35(2): 139-143, 180.   2020, 27(13): 7873-7885.
   237   238   239   240   241   242   243   244   245   246   247