[1] Qin Y H,Guillory J K,Schoenwald R D. Formulation,in vitro dissolution,and ocular bioavailability of high- and low-melting phenylephrine oxazolidines[J]. Pharmaceutical Research,1993,10(11):1627-1631.[2] Dewani A P,Dabhade S M,Bakal R L. Development and validation of a novel RP-HPLC method for simultaneous determination of paracetamol,phenylephrine hydrochloride,caffeine,cetirizine and nimesulide in tablet formulation[J]. Arabian Journal of Chemistry,2013,4(5):501-505.[3] 王琰,陈文静,周颖,等. 纤维素衍生物手性固定相拆分肾上腺素、盐酸去氧肾上腺素[J]. 药物分析杂志,2012,32(11):1985-1990.[4] 金有豫. 药理学[M]. 第5版. 北京:人民卫生出版社,2001:39.[5] Ma J,Wu L N,Hou Z,et al. Visualizing the endocytosis of phenylephrine in living cells by quantum dot-based tracking[J]. Biomaterials,2014,35:7042-7049.[6] 于彩岩,王海,李晓光,等. 盐酸去氧肾上腺素光学异构体测定方法研究[J]. 内蒙古石油化工,2010(4):9-10.[7] Dousa M,Gibala P,Havlicek J,et al. Drug-excipient compatibility testing-Identification and characterization of degradation products of phenylephrine in several pharmaceutical formulations against the common cold[J]. Journal of Pharmaceutical and Biomedical Analysis,2011,55:949-956.[8] 倪永年,桂怿. 微分脉冲伏安法测定药物中盐酸去氧肾上腺素的含量[J]. 南昌大学学报,2009,33(1):35-37.[9] Legerlotz H. Monohydric amino alcohols and their derivatives:DE,566578[P]. 1927-03-22.[10] Legerlotz H. Optically active monohydroxyphenylalkylamines:DE,543529[P]. 1929-05-28.[11] Legerlotz H. Optically active amino alcohols:DE,585164[P]. 1932-06-12.[12] Legerlotz H. Beta-alkyl-amino compounds of mono-hydroxy-phenyl- ethanols and process of producing same:US,1932347[P]. 1933-10- 24.[13] 马志聪. 一种去氧肾上腺素的制备方法:中国,101921197[P]. 2010-12-22.[14] Dousa M,Gibala P,Havlicek J,et al. Drug-excipient compatibility testing-Identification and characterization of degradation products of phenylephrine in several pharmaceutical formulations against the common cold[J]. Journal of Pharmaceutical and Biomedical Analysis,2011,55:949-956.[15] Bergamann E D,Sulzbacher M. A new synthesis of 1-(m- and p-hydroxyphenyl)-2-methylaminoethanol (m- and p-sympathol)[J]. Journal of Organic Chemistry,1951,16:84-89.[16] Sun X Y,Rai R,Deschamps J R. Boc-protected 1-(3-oxocycloalkyl) ureas via a one-step Curtius rearrangement:Mechanism and scope[J]. Tetrahedron Letters,2014,55:842-844.[17] Russel P B,Childress S J. New route to phenylephrine[J]. Journal of Pharmaceutical Sciences,1961,50:713-714.[18] Hussain A A,Truelove J E,Lawrence,et al. Ester of 3-hydroxy-α- [(methylamino)methyl]benzyl alcohol:US,3825583[P]. 1974-07-23.[19] Baison W,Teerawutgulrag A,Puangsombat P. An alternative synthesis of (±)-phenylephrine hydrochloride[J]. Maejo International Journal of Science and Technology,2014,8(01):41-47.[20] Shimojuh N,Imura Y,Moriyama K,et al. Wittig reaction with ion-supported Ph3P[J]. Tetrahedron,2011,67:951-957.[21] Bao W N,Pan H F,Zhang Z H,et al. Isolation of the stable strain Labrys sp. BK-8 for L-(+)-tartaric acid production[J]. Journal of Bioscience and Bioengineering,2014,118(1):1-5.[22] 欧阳敬平,马国振,贾娴. 动态动力学拆分中外消旋化方法的研究进展[J]. 沈阳药科大学学报,2014,31(8):654-657.[23] 李渤,李晓光,王晓红. L-去氧肾上腺素的制备方法:中国,103772215[P]. 2014-02-19.[24] 杨少容,胡先明. 手性醇类化合物的构型翻转[J]. 化学试剂,2001,23(1):15-20.[25] Prasad Divi M K,Krishna L M,Nageswara Rao B,et al. Process for resolution of 1-(3-hydroxyphenyl)-2-methylamino ethanol:US,8455692[P]. 2013-06-04.[26] Tong S Q,Guan Y X,Yan J Z. Enantiomeric separation of (R,S)-naproxen by recycling high speed counter-current chromatography with hydroxypropyl-β-cyclodextrin as chiral selector[J]. Journal of Chromatography A,2011,1218:5434-5440.[27] Gurjar M K,Krishna L M,Sarma B V N B S,et al. A practical synthesis of (R)-(-)-phenylephrine hydrochloride[J]. Organic Process Research & Development,1998,2(6):422-424.[28] Larrow J F. Industrial applications of the jacobsen hydrolytic kinetic resolution technology[J]. Comprehensive Chirality,2012,9:129-146.[29] Khan N H,Sadhukhan A,Maity N C,et al. Enantioselective O-acetylcyanation/cyanoformylation of aldehydes using catalysts with built-in crown ether-like motif in chiral macrocyclic V(Ⅴ) Salen complexes[J]. Tetrahedron,2011,67:7073-7080.[30] 程咏梅. 化学酶法催化仲醇的动态动力学拆分[D]. 杭州:浙江大学,2010.[31] 张怡. 氰醇及不饱和仲醇的动力学拆分研究[D]. 上海:东华大学,2011.[32] Baumgarten W,Schiffers R. Process for manufacturing of enantiomerically pure 3-hydroxy-3-phenyl-propylamin:US,7294744[P]. 2007-11-13.[33] Takeda H,Tachinami T,Aburatani M,et al. Practical asymmetric synthesis of (R)-(-)-phenylephrine hydrochloride catalyzed by (2R,4R)-MCCPM-Rhodium complex[J]. Tetrahedron Letters,1989,30(3):367-370.[34] Sakuraba S,Takahashi H,Takeda T,et al. Efficient asymmetric hydrogenation of α-amino ketone derivatives. A highly enantioselective synthesis of phenylephrine,levamisole,carnitine and propranolol[J]. Chemical and Pharmaceutical Bulletin,1995,43(5):738-747.[35] Klingler F D,Wolter L,Dietrich W,et al.Verfahren zur herstellung von L-phenylephrin hydrochlorid:DE,19902229[P]. 2002-02-20.[36] Hossein Michaelson. Synthesis of enantiomerically pure 2-hydroxy- 2-aryl-ethylamines:WO,2009086283[P]. 2008-11-22.[37] McGarrity J F,Zanotti-Gerosa A. A feasibility study on the synthesis of phenylephrine via ruthenium-catalyzed homogeneous asymmetric hydrogenation[J]. Tetrahedron:Asymmetry,2010(21):2479-2486.[38] 冯文化,郭方超,于晓丽. L-苯福林盐酸盐的制备方法:中国,102234237[P]. 2011-10-27.[39] Xing X Y,Zhao Y H,Xu C,et al. Electronic helix theory-guided rational design of kinetic resolutions by means of the Sharpless asymmetric dihydroxylation reactions[J]. Tetrahedron,2012,68:7288-7294.[40] Devi R,Borah R,Deka C R. Design of zeolite catalysts for Henry reaction under mild condition[J]. Applied Catalysis A:General,2012,433:122-127.[41] Rajesh K P,Puspesh K U,Pradeep K. Enantioselective synthesis of (R)-phenylephrine hydrochloride[J]. Tetrahedron Letters,2003,44:6245-6246.[42] Kureshy R I,Dangi B,Das A,et al. Recyclable Cu(Ⅱ)-macrocyclic salen complexes catalyzed Henry reaction of aldehydes:A practical strategy in the preparation of (R)-phenylephrine[J]. Applied Catalysis A:General,2012(439):74-79.[43] Kureshy R I,Das A,Khan N H,et al. Cu(Ⅱ)-Macrocylic[H4]salen catalyzed asymmetric Henry reaction and its application in the synthesis of α1-adrenergic receptor agonist (R)-phenylephrine[J]. ACS Catalysis,2011,1(11):1529-1535.[44] Alvizo O,Collier S J,Hennemann J,et al. Ketoreductase polypeptides for the preparation of phenylephrine:US,20120149073[P]. 2012-06-14.[45] Lin W D,Chen C Y,Chen H C,et al. Enantioselective synthesis of (S)-phenylephrine by whole cells of recombinant escherichia coli expressing the amino alcohol dehydrogenase gene from rhodococcus erythropolis BCRC 10909[J]. Process Biochemistry,2010,45:1529-1536.[46] Peng G J,Cho Y C,Fu T K,et al. Enantioselective synthesis of (S)-phenylephrine by recombinant escherichia coli cells expressing the short-chain dehydrogenase/reductase gene from serratia quinivorans BCRC 14811[J]. Process Biochemistry,2013,48:1509-1515.[47] Peng G J,Kuan Y C,Chou H Y,et al. Stereoselective synthesis of (R)-phenylephrine using recombinant escherichia coli cells expressing a novel short-chain dehydrogenase/reductase gene from serratia marcescens BCRC 10948[J]. Journal of Biotechnology,2014,170:6-9.[48] LenoX H J,Terentieva E,Gololobov M Y,et al. Optically active fiuorinated vasoconstrictors,methods for making them,and anesthetic formulations comprising them:US,6900203[P]. 2005-05-31.[49] Tokoshima D,Hanaya K,Shoji M,et al. Whole-cell yeast-mediated preparation of (R)-2-chloro-1-(3-nitrophenyl)ethanol as a synthetic precursor for (R)-phenylephrine[J]. Journal of Molecular Catalysis B:Enzymatic,2013,97:95-99.[50] Jin Z,Han S Y,Zhang L,et al. Combined utilization of lipase-displaying pichia pastoris whole-cell biocatalysts to improve biodiesel production in co-solvent media[J]. Bioresource Technology,2013,130:102-109.[51] Navarro R,Ruiz P,Saucedo I,et al. Bismuth(Ⅲ) recovery from hydrochloric acid solutions using Amberlite XAD-7 impregnated with a tetraalkylphosphonium ionic liquid[J]. Separation and Purification Technology,2014,135:268-277.[52] Jahani F,Tajbakhsh M,Golchoubian H,et al. Guanidine hydrochloride as an organocatalyst for N-Boc protection of amino groups[J]. Tetrahedron Letters,2011,52:1260-1264.[53] Valizadeh H,Shomali A,Nourshargh S,et al. Carboxyl and nitrite functionalized graphene quantum dots as a highly active reagent and catalyst for rapid diazotization reaction and synthesis of azo-dyes under solvent-free conditions[J]. Dyes and Pigments,2015,113:522-528.[54] 王波,孙勇,文军. 一种去氧肾上腺素的制备方法:中国,102776251[P]. 2012-08-21.[55] Breuer M,Pletsch A,Hauer B,et al. Method for producing L-phenylephring using an alcohol dehydrogenase of aromaticum EBN1:US,8617854[P]. 2013-12-31. |