2835-06-5 = 875-74-1 [标题:Reaction Conditions 标题:D(-)-α-Phenylglycine 参考文献:Federal Republic Of Germany]
6485-67-2 = 875-74-1 反应条件:1.1 Reagents: Hydrochloric Acid,Sulfuric Acid Solvents: Water; 120 Min,Ph 8,277 K 标题:Enzyme Distribution Derived From Macroscopic Particle Behavior Of An Industrial Immobilized Penicillin-G Acylase 作者:Van Roon,Jeroen L.; Et Al 参考文献:Biotechnology Progress 日期:2003 卷标:19(5) 页码:1510-1518]
6485-67-2 = 875-74-1 反应条件:1.1 Catalysts: Penicillin Amidase Solvents: Water; 4 H,Ph 7.5,25 °C 标题:Enzyme Catalyzed Biotransformations In Aqueous Two-Phase Systems With Precipitated Substrate And/or Product 作者:Kasche,V.; Et Al 参考文献:Biotechnology And Bioengineering 日期:1995 卷标:45(3) 页码:261-7]
33125-05-2 = 875-74-1 反应条件:1.1 Reagents: Trifluoroacetic Acid Solvents: Dichloromethane; 3 H,Rt1.2 Reagents: Sodium Carbonate Solvents: Water; Ph 9 标题:In Vitro Synthesis Of New Cyclodepsipeptides Of The Pf1022-Type: Probing The α-D-Hydroxy Acid Tolerance Of Pf1022 Synthetase 作者:Mueller,Jane; Et Al 参考文献:Chembiochem 日期:2009 卷标:10(2) 页码:323-328]
6489-76-5 = 875-74-1 反应条件:1.1 Reagents: Sodium Dodecylsulfonate,Sodium Nitrite,Sulfuric Acid Solvents: 1-Pentanol 标题:Chemoenzymatic Synthesis Of D-Phenylglycine 作者:Li,Jun; Et Al 参考文献:Zhongguo Yaoke Daxue Xuebao 日期:2000 卷标:31(4) 页码:294-296]
29125-25-5 = 875-74-1 反应条件:1.1 Reagents: Hydrogen Catalysts: Palladium Solvents: Acetic Acid,Water 标题:The Asymmetric Synthesis Of α-Amino Acids. Electrophilic Azidation Of Chiral Imide Enolates,A Practical Approach To The Synthesis Of (R)- And (S)-α-Azido Carboxylic Acids 作者:Evans,David A.; Et Al 参考文献:Journal Of The American Chemical Society 日期:1990 卷标:112(10) 页码:4011-30]
100-52-7 = 875-74-1 反应条件:1.1 Reagents: Ammonium Acetate Solvents: Water; 30 Min,Ph 8,20 °C1.2 Catalysts: Nitrilase 标题:Chemoenzymatic Method For Enantioselective Synthesis Of (R)-2-Phenylglycine And (R)-2-Phenylglycine Amide From Benzaldehyde And Kcn Using Difference Of Enzyme Affinity To The Enantiomers 作者:Kawahara,Nobuhiro; Et Al 参考文献:Chemcatchem 日期:2018 卷标:10(21) 页码:5014-5020]
455875-26-0 = 875-74-1 反应条件:1.1 Reagents: Hydrochloric Acid Solvents: Water; 3 H,110 °C 标题:Enantioselective Hydrocyanation Of N-Protected Aldimines 作者:Uemura,Masato; Et Al 参考文献:Organic Letters 日期:2012 卷标:14(3) 页码:882-885]
= 875-74-1 反应条件:1.1 Reagents: Lithium Hydroxide Solvents: Tetrahydrofuran,Water 标题:Asymmetric Synthesis Of α-Amino Acids And α-N-Hydroxyamino Acids From N-Acylbornane-10,2-Sultams: 1-Chloro-1-Nitrosocyclohexane As A Practical [nh2+] Equipment 作者:Oppolzer,Wolfgang; Et Al 参考文献:Helvetica Chimica Acta 日期:1992 卷标:75(6) 页码:1965-78]
188772-75-0 = 875-74-1 反应条件:1.1 Reagents: Sodium Periodate Catalysts: Ruthenium Dioxide Solvents: Carbon Tetrachloride,Acetonitrile,Water; 30 Min1.2 2 H 标题:Novel Enantioselective Synthesis Of Both Enantiomers Of Furan-2-Yl Amines And Amino Acids 作者:Demir,Ayhan; Et Al 参考文献:Helvetica Chimica Acta 日期:2003 卷标:86(1) 页码:91-105]
= 875-74-1 反应条件:1.1 Reagents: Hydrogen Catalysts: Palladium Dihydroxide Solvents: Ethanol 标题:Asymmetric Induction. Ii. Phase Transfer-Catalyzed Reaction Of Benzaldehyde With Chloroform And Chiral Amines 作者:Shi,Yaozeng; Et Al 参考文献:Youji Huaxue 日期:1987 卷标:(5) 页码:350-3]
6485-67-2 = 875-74-1 反应条件:1.1 Reagents: Hydrochloric Acid Solvents: Water 标题:Practical And Convenient Enzymatic Synthesis Of Enantiopure α-Amino Acids And Amides 作者:Wang,Mei-Xiang; Et Al 参考文献:Journal Of Organic Chemistry 日期:2002 卷标:67(18) 页码:6542-6545]
700-63-0 = 875-74-1 反应条件:1.1 Reagents: Pyridoxal 5′-Phosphate Catalysts: 2-Aminohexano-6-Lactam Racemase,D-Amino Acid Amidase Solvents: Water; 24 H,Ph 8,40 °C 标题:Enzymatic Synthesis Of Chiral Phenylalanine Derivatives By A Dynamic Kinetic Resolution Of Corresponding Amide And Nitrile Substrates With A Multi-Enzyme System 作者:Yasukawa,Kazuyuki; Et Al 参考文献:Advanced Synthesis & Catalysis 日期:2012 卷标:354(17) 页码:3327-3332]
700-63-0 = 875-74-1 反应条件:1.1 Reagents: Tripotassium Phosphate Catalysts: Amidase Solvents: Water2.1 Reagents: Hydrochloric Acid Solvents: Water 标题:Practical And Convenient Enzymatic Synthesis Of Enantiopure α-Amino Acids And Amides 作者:Wang,Mei-Xiang; Et Al 参考文献:Journal Of Organic Chemistry 日期:2002 卷标:67(18) 页码:6542-6545]
6489-76-5 = 875-74-1 [标题:Reaction Conditions 标题:Enzymic Conversion Of N-Carbamoyl-D-Amino Acids To D-Amino Acids 作者:Olivieri,R.; Et Al 参考文献:Enzyme And Microbial Technology 日期:1979 卷标:1(3) 页码:201-4]
1207847-57-1 = 875-74-1 反应条件:1.1 Reagents: Hydrochloric Acid Solvents: Methanol,Water; 70 °C; 5 Min,70 °C1.2 Reagents: Ammonium Hydroxide Solvents: Water 标题:Resolution/deracemization Of Chiral α-Amino Acids Using Resolving Reagents With Flexible Stereogenic Centers 作者:Soloshonok,Vadim A.; Et Al 参考文献:Journal Of The American Chemical Society 日期:2009 卷标:131(21) 页码:7208-7209]
= 875-74-1 反应条件:1.1 Reagents: Hydrochloric Acid Solvents: Acetonitrile,Water; 20 Min,Rt1.2 Reagents: Potassium Hexafluorophosphate Solvents: Water; 20 Min,Rt 标题:Diastereoselective Photooxidation And Reduction Of Chiral Iridium(Iii) Complexes 作者:Li,Li-Ping; Et Al 参考文献:Inorganic Chemistry 日期:2019 卷标:58(1) 页码:785-793]
89-24-7 = 875-74-1 [标题:Reaction Conditions 标题:Enzymic Conversion Of N-Carbamoyl-D-Amino Acids To D-Amino Acids 作者:Olivieri,R.; Et Al 参考文献:Enzyme And Microbial Technology 日期:1979 卷标:1(3) 页码:201-4]
89-24-7 = 875-74-1 [标题:Reaction Conditions 标题:Microbial Transformation Of Hydantoins To Amino Acids. Iii. Microbial Transformation Of Hydantoins To N-Carbamyl-D-Amino Acids 作者:Takahashi,Satomi; Et Al 参考文献:Journal Of Fermentation Technology 日期:1979 卷标:57(4) 页码:328-32]
138-18-1 = 875-74-1 [标题:Reaction Conditions 标题:A Stereo-Inverting D-Phenylglycine Aminotransferase From Pseudomonas Stutzeri St-201: Purification,Characterization And Application For D-Phenylglycine Synthesis 作者:Wiyakrutta,Suthep; Et Al 参考文献:Journal Of Biotechnology 日期:1997 卷标:55(3) 页码:193-203]
188200-11-5 = 875-74-1 反应条件:1.1 Reagents: Sodium Periodate Solvents: Carbon Tetrachloride,Acetonitrile,Water1.2 Reagents: Ruthenium Trichloride Solvents: Dichloromethane 标题:Reversal Of The Stereochemical Course Of The Addition Of Phenylmagnesium Bromide To N-Benzylimines Derived From R-Glyceraldehyde Depending On The O-Protecting Group And Its Application To The Synthesis Of Both Enantiomers Of Phenylglycine 作者:Badorrey,Ramon; Et Al 参考文献:Tetrahedron 日期:1997 卷标:53(4) 页码:1411-1416]
14257-84-2 + 42429-20-9 = 875-74-1 反应条件:1.1 Reagents: Potassium Hydroxide,Cobalt Chloride (Cocl2) Catalysts: Amidase Solvents: Water; 30 Min,Ph 7.5,40 °C 标题:Enzymic Resolution Of Dl-Phenylglycine 作者:Machado,Georgia D. C.; Et Al 参考文献:Process Biochemistry (Oxford 日期:2005 卷标:40(10) 页码:3186-3189]
219924-26-2 = 875-74-1 反应条件:1.1 Reagents: Hydrochloric Acid Solvents: Methanol 标题:Enhanced Diastereoselectivity In The Asymmetric Ugi Reaction Using A New "Convertible" Isonitrile 作者:Linderman,Russell J.; Et Al 参考文献:Journal Of Organic Chemistry 日期:1999 卷标:64(2) 页码:336-337
专利号:WO-8800592-A1 优先权日:1986-07-18 标题:DIASTEROSELECTIVE STRECKER SYNTHESIS OF alpha-AMINOACIDS FROM GLYCOSYLAMINE DERIVATES 发明人:KUNZ HORST; SAGER WILFRIED; PFRENGE WALDEMAR; DECKER MATHIAS 权利人:CELAMERCK GMBH & CO KG 摘要:O-acyl-protected glycosylamines, in particular 2,3,4,6-tetra-O-pivaloyl-beta-D-galactopyranosylamine (1), their preparation and their use for the diastereoselective synthesis of alpha-aminoacids. With compounds such as (1), one can obtain by Strecker synthesis high yields and high diastereomer surplus. The direction of the asymmetric induction can be determined by the selection of the solvent. This type of synthesis is particularly effective when carried with Lewis acid catalysts. One obtains also high yields and high diastereoselectivity during Ugi four component synthesis facilitated by Lewis acids by using amines such as (1).
专利号:US-7317129-B2 优先权日:2002-06-07 标 题:Chemical synthesis of reagents for peptide coupling 发明人:RAINES RONALD T; KIESSLING LAURA L; NILSSON BRADLEY L; HE YI; SOELLNER MATTHEW B; HINKLIN RONALD J 权利人:WISCONSIN ALUMNI RES FOUND 摘要:The present invention provides improved methods for synthesis of phosphinothiol reagents, as well as novel protected reagents, for use in formation of amide bonds, and particularly, for peptide ligation. The invention provides phosphine-borane complexes useful as reagents in the formation of amide bonds, particularly for the formation of an amide bond between any two of an amino acid, a peptide, or a protein.
专利号:EP-2173892-B8 优先权日:2007-07-27 标题:Process for the preparation of immobilised recombinant Penicillin Acylase biocatalyst from Achromobacter sp CCM 4824 expressed in E. coli BL21 CCM 7394 and its use for the synthesis of beta-lactam antiobiotics 发明人:DATLA ANUPAMA; RAJASEKAR VYASARAYANI WILLIAMS; KYSLIK PAVEL; BECKA STANISLAV; KRISHNAKANT ASHAR TRUPTI; YOGESH ZAMBRE SUJATA; NIKUNJ KUMAR 权利人:FERMENTA BIOTECH LTD 摘要:The present invention discloses isolation of Penicillin Acylase (PA) from Achromobacter sp CCM 4824 expressed in recombinant strain E. coli BL21 CCM 7394 bearing the recombinant plasmid pKXIP1 and processing of PA into biocatalyst useful for the industrial synthesis of antibiotics. More particularly the invention discloses a synthesis of semi-synthetic β-lactam antibiotics in the reaction mixture consisting of activated acyl-donor (D-p-hydroxyphenylglycine methyl ester or amide for Amoxicillin and Cefadroxil; D-phenylglycine methyl ester or amide for Ampicillin and Cephalexin) and nucleophile (6-APA or 7-ADCA) catalyzed by PA obtained from recombinant E. coli BL21 CCM 7394 as the biocatalyst.
专利号:US-2010105111-A1 优先权日:2007-02-28 标 题 :Method for production of optically active amino acid 发明人:ASANO YASUHISA; TANAKA AKINORI; HASEMI RYUJI 权利人:MITSUBISHI GAS CHEMICAL CO 摘要:An optically active amino acid is useful as food or feed, agrochemicals, chemical products for industrial use, intermediates for synthesis of cosmetics or medicines and the like and is also important as optical resolving agents or chiral building blocks for use in organic synthesis. Thus, the object is to provide an industrially practical method for producing the optically active amino acid simply and at low cost. The method comprises the step of reacting an aminonitrile composed of a mixture of a D-aminonitrile and an L-aminonitrile with a biocatalyst which is one derived from a newly isolated microorganism belonging to the genus Rhodococcus and has an activity of converting the two aminonitriles into a D-amino acid amide and an L-amino acid amide respectively, a biocatalyst which has an activity of racemizing the D-amino acid amide and the L-amino acid amide to each other, and a biocatalyst which has an activity of converting one of the D-amino acid amide and the L-amino acid amide into the corresponding D- or L-amino acid.
专利号:US-2018312463-A1 优先权日:2015-10-22 标题:Synthesis of Cyclohexane Carboxamide Derivatives Useful as Sensates in Consumer Products 发明人:YELM KENNETH EDWARD; WOS JOHN AUGUST; BUNKE GREGORY MARK; FREDERICK HEATH; HAUGHT JOHN CHRISTIAN; HOKE STEVEN HAMILTON; SREEKRISHNA KOTI TATACHAR; LIN YAKANG 权利人:PROCTER & GAMBLE 摘要:Synthesis methods to produce a series of carboxamides built off of an (S)-2-amino acid backbone or an (R)-2-amino acid backbone, depending upon the desired diastereomer of the end product.
专利号:US-5856492-A 优先权日:1997-01-10 标题 :Efficient synthesis of a chiral mediator 发明人:CHEN CHENG YI; XU FENG; TILLYER RICHARD D; ZHAO DALIAN 权利人:MERCK & CO INC 摘要:An efficient method for the quantitative preparation and isolation of a compound of formula I ##STR1## or its enantiomer, a chiral mediator used in enantioselective synthesis.
[参考文献]: Luckose F, Et Al. Effects Of Amino Acid Derivatives On Physical, Mental, And Physiological Activities. Crit Rev Food Sci Nutr. 2015;55(13):1793-1144. [参考文献]: Aaron D Mills, Et Al. Design And Synthesis Of A Hybrid Potentiator-Corrector Agonist Of The Cystic Fibrosis Mutant Protein Deltaf508-Cftr. Bioorg Med Chem Lett. 2010 Jan 1;20(1):87-91. [参考文献]: Antonella Caputo, Et Al. Mutation-Specific Potency And Efficacy Of Cystic Fibrosis Transmembrane Conductance Regulator Chloride Channel Potentiators. J Pharmacol Exp Ther. 2009 Sep;330(3):783-91. [参考文献]: Choedchai Saehuan, Et Al. Isolation And Characterization Of A Benzoylformate Decarboxylase And A Nad+/nadp+-Dependent Benzaldehyde Dehydrogenase Involved In D-Phenylglycine Metabolism In Pseudomonas Stutzeri St-201. Biochim Biophys Acta. 2007 Nov;1770(11):1585-92. [参考文献]: Hiroomi Nagata, Et Al. Structural Scaffold Of 18-Crown-6 Tetracarboxylic Acid For Optical Resolution Of Chiral Amino Acid: X-Ray Crystal Analyses And Energy Calculations Of Complexes Of D- And L-Isomers Of Tyrosine, Isoleucine, Methionine And Phenylglycine. Org Biomol Chem. 2004 Dec 7;2(23):3470-5.
合成参考文献
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