{"id":4050,"date":"2020-09-30T15:25:19","date_gmt":"2020-09-30T06:25:19","guid":{"rendered":"https:\/\/www.hamarichemicals.com\/eng\/?page_id=4050"},"modified":"2022-01-26T14:06:16","modified_gmt":"2022-01-26T05:06:16","slug":"hamari-historical-publication-list","status":"publish","type":"page","link":"https:\/\/www.hamarichemicals.com\/eng\/technology\/publication-list\/hamari-historical-publication-list\/","title":{"rendered":"Historical Publications"},"content":{"rendered":"
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\n

Hamari’s Past Scientific Publications<\/h1>\n

More publications.<\/strong> The following is a list of historical publications authored by Hamari.<\/p>\n

Selected List of Published Research<\/h3>\n

The following is a selected list of peer-reviewed research articles authored by Hamari Chemicals, Ltd.<\/p>\n

    \n
  1. Tandem alkylation\u2212second-order asymmetric transformation protocol for the preparation of phenylalanine-type tailor-made \u03b1\u2011amino acids.\u00a0<\/strong>ACS Omega <\/em> 2018<\/strong>, 3<\/em>, 9729\u20139737. DOI: 10.1021\/acsomega.8b01424<\/li>\n
  2. Second-order asymmetric transformation and its application for the practical synthesis of \u03b1-amino acids. <\/strong>Org. Biomol. Chem.<\/em> 2018<\/strong>, 16<\/em>, 4968\u20134972. DOI: 10.1039\/C8OB00963E<\/li>\n
  3. 2-Pyrrolidinecarboxamide, N<\/em>-(2-Benzoyl-4-chlorophenyl)-1-[(3,4-dichlorophenyl)methyl]-,(2R<\/em>)- and (2S<\/em>)-. <\/strong>e-EROS reagent article.<\/em> DOI: 10.1002\/047084289X.rn02164<\/li>\n
  4. Axially chiral Ni(II) complexes of \u03b1\u2010amino acids: Separation of enantiomers and kinetics of racemization. <\/strong>Chirality<\/em> 2018<\/strong>, 30<\/em>, 498\u2013508. DOI: 10.1002\/chir.2281<\/li>\n
  5. Identification of novel plasminogen activator inhibitor-1 inhibitors with improved oral bioavailability: Structure optimization of N<\/em>-acylanthranilic acid derivatives.\u00a0<\/strong>Bioorg. Med. Chem. Lett. <\/em> 2018<\/strong>, 28<\/em>, 809\u2013813. DOI: 10.1016\/j.bmcl.2017.11.016<\/li>\n
  6. \u5065\u5eb7\u6210\u4eba\u7537\u6027\u306b\u304a\u3051\u308b\u30e2\u30f3\u30c6\u30eb\u30ab\u30b9\u30c8\u30c1\u30e5\u30a2\u30d6\u30eb\u93205 mg\u300cAA\u300d\/\u300c\u30a2\u30b9\u30da\u30f3\u300d\/\u300c\u30aa\u30fc\u30cf\u30e9\u300d\u306e\u751f\u7269\u5b66\u7684\u540c\u7b49\u6027\u8a66\u9a13. <\/strong>\u81e8\u5e8a\u533b\u85ac<\/em> 2017<\/strong>, 33<\/em>, 5<\/em>, 443\u2013468. ISSN: 0910-8211<\/li>\n
  7. An N<\/em>-protection free ligation of the peptide thioester and the peptide with an N<\/em>-alkoxy- or N<\/em>-aryloxyamino group at its N<\/em>-terminus.\u00a0<\/strong>Tetrahedron Lett.<\/em>\u00a02017<\/strong>,\u00a058<\/em>, 4638\u20134641. DOI: 10.1016\/j.tetlet.2017.10.074<\/li>\n
  8. Analysis of crystallographic structures of Ni(II) complexes of \u03b1-amino acid Schiff bases: Elucidation of the substituent effect on stereochemical preferences.\u00a0<\/strong>Dalton Trans. <\/em> 2017<\/strong>, 46<\/em>, 4191\u20134198. DOI: 10.1039\/C7DT00014F<\/li>\n
  9. Operationally convenient and scalable asymmetric synthesis of (2S<\/em>)- and (2R<\/em>)-\u03b1-(methyl)cysteine derivatives through alkylation of chiral alanine schiff base NiII<\/sup> complexes\u00a0<\/strong>Eur. J. Org. Chem. <\/em>2017<\/strong>, 14<\/em>, 1931\u20131939. DOI: 10.1002\/ejoc.201700018<\/li>\n
  10. Scale-up synthesis of (R<\/em>)- and (S<\/em>)-N<\/em>-(2-Benzoyl-4-chlorophenyl)-1-(3,4-dichlorobenzyl) pyrrolidine-2-carboxamide hydrochloride, a versatile reagent for the preparation of tailor-made \u03b1- and \u03b2-amino acids in an enantiomerically pure form. <\/strong>Org. Process Res. Dev. <\/em> 2017<\/strong>, 21<\/em>, 732\u2013739. DOI: 10.1021\/acs.oprd.7b00055<\/li>\n
  11. Recent approaches for asymmetric synthesis of \u03b1-amino acids via<\/em> homologation of Ni(II) complexes.\u00a0<\/strong>Amino Acids <\/em> 2017<\/strong>, 49<\/em>, 1487\u20131520. DOI: 10.1007\/s00726-017-2458-6<\/li>\n
  12. Asymmetric synthesis of \u03b1-deuterated \u03b1-amino acids.\u00a0<\/strong>Org. Biomol. Chem. <\/em>2017<\/strong>, 15<\/em>, 6978\u20136983. DOI: 10.1039\/C7OB01720K<\/li>\n
  13. Unprecedented property of 4,6-di(substituted)amino-1,2-dihydro-1,3,5-triazines: Formation of acid salts by simple treatment with alkali metal salts of protic acids.\u00a0<\/strong>Bull. Chem. Soc. Jpn.<\/em> 2017<\/strong>, 90<\/em>, 178\u2013187. DOI: 10.1246\/bcsj.20160329<\/li>\n
  14. Purely chemical approach for preparation of D-\u03b1-amino acids via<\/em> (S<\/em>)-to-(R<\/em>)-interconversion of unprotected tailor-made \u03b1-amino acids.\u00a0<\/strong>J. Org. Chem.<\/em> 2016<\/strong>, 81<\/em>, 3501\u20133508. DOI: 10.1021\/acs.joc.5b02707<\/li>\n
  15. Asymmetric synthesis of aromatic and heteroaromatic \u03b1-amino acids using a recyclable axially chiral ligand.\u00a0<\/strong>Eur. J. Org. Chem.<\/em> 2016<\/strong>, 5<\/em>, 999\u20131006. DOI: 10.1002\/ejoc.201501442<\/li>\n
  16. Advanced asymmetric synthesis of (1R<\/em>,2S<\/em>)-1-amino-2-vinylcyclopropanecarboxylic acid by alkylation\/cyclization of newly designed axially chiral Ni(II) complex of glycine Schiff base.\u00a0<\/strong>Amino Acids<\/em> 2016<\/strong>, 48<\/em>, 973\u2013986. DOI: 10.1007\/s00726-015-2138-3<\/li>\n
  17. Recyclable ligands for the non-enzymatic dynamic kinetic resolution of challenging \u03b1-amino acids.\u00a0<\/strong>Angew. Chem. Int. Ed.<\/em> 2015<\/strong>, 54<\/em>, 12918\u201312922. DOI: 10.1002\/anie.201507273<\/li>\n
  18. Chemical dynamic thermodynamic resolution and S\/R<\/em> interconversion of unprotected unnatural tailor-made \u03b1-amino acids.\u00a0<\/strong>J. Org. Chem.<\/em> 2015<\/strong>, 80<\/em>, 9817\u20139830. DOI: 10.1021\/acs.joc.5b01292<\/li>\n
  19. Asymmetric synthesis of (1R<\/em>,2S<\/em>)-1-amino-2-vinylcyclopropanecarboxylic acid by sequential SN<\/sub>2\u2013SN<\/sub>2\u2019 dialkylation of (R<\/em>)-N<\/em>-(benzyl)proline-derived glycine Schiff base Ni(II) complex.\u00a0<\/strong>RSC Adv.<\/em> 2015<\/strong>, 5<\/em>, 1051\u20131058. DOI: 10.1039\/C4RA12658K<\/li>\n
  20. Synthesis of (2S<\/em>,3S<\/em>)-\u03b2-(trifluoromethyl)-\u03b1,\u03b2-diamino acid by Mannich addition of glycine Schiff <\/strong>base Ni(II) complexes to N<\/em>–tert<\/em>-butylsulfinyl-3,3,3-trifluoroacetaldimine.\u00a0<\/strong>J. Fluorine Chem.<\/em> 2015<\/strong>, 171<\/em>, 67\u201372. DOI: 10.1016\/j.jfluchem.2014.09.013<\/li>\n
  21. Chemical dynamic kinetic resolution and S\/R<\/em> interconversion of unprotected \u03b1-amino acids.\u00a0<\/strong>Angew. Chem. Int. Ed.<\/em> 2014<\/strong>, 53<\/em>, 12214\u201312217. DOI: 10.1002\/anie.201407944<\/li>\n
  22. Flavin-catalyzed aerobic oxidation of sulfides and thiols with formic acid\/triethylamine.\u00a0<\/strong>Chem. Commun.<\/em> 2014<\/strong>, 50<\/em>, 10295\u201310298. DOI: 10.1039\/C4CC05216A<\/li>\n
  23. Design and synthesis of (S<\/em>)- and (R<\/em>)-\u03b1-(phenyl)ethylamine-derived NH-type ligands and their application for the chemical resolution of \u03b1-amino acids.\u00a0<\/strong>Org. Biomol. Chem.<\/em> 2014<\/strong>, 12<\/em>, 6239\u20136249. DOI: 10.1039\/C4OB00669K<\/li>\n
  24. Asymmetric synthesis of \u03b1-amino acids under operationally convenient conditions.\u00a0<\/strong>Adv. Synth. Catal.<\/em> 2014<\/strong>, 356<\/em>, 2203\u20132208. DOI: 10.1002\/adsc.201400405<\/li>\n
  25. Asymmetric synthesis of \u03b1-amino acids via<\/em> homologation of Ni(II) complexes of glycine Schiff bases. Part 3: Michael addition reactions and miscellaneous transformations.\u00a0<\/strong>Amino Acids<\/em> 2014<\/strong>, 46<\/em>, 2047\u20132073. DOI: 10.1007\/s00726-014-1764-5<\/li>\n
  26. Inexpensive chemical method for preparation of enantiomerically pure phenylalanine.\u00a0<\/strong>Amino Acids<\/em> 2014<\/strong>, 46<\/em>, 945\u2013952. DOI: 10.1007\/s00726-013-1656-0<\/li>\n
  27. Synthesis and stereochemical assignments of diastereomeric Ni(II) complexes of glycine Schiff base with (R<\/em>)-2-(N<\/em>-{2-[N<\/em>-alkyl-N<\/em>-(1-phenylethyl)amino]acetyl}amino)benzophenone; A case of configurationally stable stereogenic nitrogen.\u00a0<\/strong>Beilstein J. Org. Chem.<\/em> 2014<\/strong>, 10<\/em>, 442\u2013448. DOI: 10.3762\/bjoc.10.41<\/li>\n
  28. NH-type of chiral Ni(II) complexes of glycine Schiff base: design, structural evaluation, reactivity and synthetic applications.\u00a0<\/strong>Org. Biomol. Chem.<\/em> 2014<\/strong>, 12<\/em>, 1278\u20131291. DOI: 10.1039\/C3OB41959B<\/li>\n
  29. Asymmetric synthesis of \u03b1-amino acids via<\/em> homologation of Ni(II) complexes of glycine Schiff bases. Part 2: Aldol, Mannich addition reactions, deracemization and (S<\/em>) to (R<\/em>) interconversion of \u03b1-amino acids.\u00a0<\/strong>Amino Acids<\/em> 2013<\/strong>, 45<\/em>, 1017\u20131033. DOI: 10.1007\/s00726-013-1580-3<\/li>\n
  30. Asymmetric synthesis of \u03b1-amino acids via<\/em> homologation of Ni(II) complexes of glycine Schiff bases; Part 1: alkyl halide alkylations.\u00a0<\/strong>Amino Acids<\/em> 2013<\/strong>, 45<\/em>, 691\u2013718. DOI: 10.1007\/s00726-013-1539-4<\/li>\n
  31. Chemical deracemization and (S<\/em>) to (R<\/em>) interconversion of some fluorine-containing \u03b1-amino acids.\u00a0<\/strong>J. Fluorine Chem.<\/em> 2013<\/strong>, 152<\/em>, 114\u2013118. DOI: 10.1016\/j.jfluchem.2013.02.022<\/li>\n
  32. Synthesis of bis-\u03b1,\u03b1\u2019-amino acids through diastereoselective bis-alkylations of chiral Ni(II)-complexes of glycine.\u00a0<\/strong>Org. Biomol. Chem.<\/em> 2013<\/strong>, 11<\/em>, 4508\u20134515. DOI: 10.1039\/C3OB40594J<\/li>\n
  33. Chemical approach for interconversion of (S<\/em>)- and (R<\/em>)-\u03b1-amino acids.\u00a0<\/strong>Org. Biomol. Chem.<\/em> 2013<\/strong>, 11<\/em>, 4503\u20134507. DOI: 10.1039\/C3OB40541A<\/li>\n
  34. Plasminogen activator inhibitor-1\u963b\u5bb3\u85ac<\/strong> Current Therapy<\/em> 2011<\/strong>, 29<\/em>, 70-73. ISSN: 02878445<\/li>\n
  35. Structure-Activity Relationships of New N<\/em>-Acylanthranilic Acid Derivatives as Plasminogen Activator Inhibitor-1 Inhibitors.<\/strong> Chem. Pharm. Bull.<\/em> 2011<\/strong>, 59<\/em>, 215\u2013224. DOI: 10.1248\/cpb.59.215<\/li>\n
  36. Effect of Carnosine and its Trolox-Modified Derivatives on Life Span of Drosophila melanogaster<\/em><\/strong>. Rejuvenation Res.<\/em> 2010<\/strong>, 13<\/em>, 453\u2013457. DOI: 10.1089\/rej.2009.1010<\/li>\n
  37. Structure\u2013Activity Relationships of New 2-Acylamino-3-thiophenecarboxylic Acid Dimers as Plasminogen Activator Inhibitor-1 Inhibitors.\u00a0<\/strong>Chem. Pharm. Bull.<\/em> 2010<\/strong>, 58<\/em>, 615\u2013619. DOI: 10.1248\/cpb.58.615<\/li>\n
  38. Bactericidal Effect of HM-242, a Novel Disinfectant, against Pseudomonas aeruginosa<\/em>.\u00a0<\/strong>Biocontrol Sci.<\/em> 2010<\/strong>, 15<\/em>, 7\u201313. DOI: 10.4265\/bio.15.7<\/li>\n
  39. A novel inhibitor of plasminogen activator inhibitor-1 provides antithrombotic benefits devoid of bleeding effect in nonhuman primates.\u00a0<\/strong> J. Cereb. Blood Flow Metab.<\/em> 2010<\/strong>, 30<\/em>, 904\u2013912. DOI: 10.1038\/jcbfm.2009.272<\/li>\n
  40. Biological Activity of Novel Synthetic Derivatives of Carnosine.\u00a0<\/strong> Cell. Mol. Neurobiol.<\/em> 2010<\/strong>, 30<\/em>, 395\u2013404. DOI: 10.1007\/s10571-009-9462-7<\/li>\n
  41. Synthesis of Novel 4,6-Di(substituted)amino-1,2-dihydro-1,3,5-triazine Derivatives as Topical Antiseptic Agents.\u00a0<\/strong>J. Med. Chem.<\/em> 2009<\/strong>, 52<\/em>, 597\u2013600. DOI: 10.1021\/jm8014712<\/li>\n
  42. In vitro<\/em> evaluation of the antimicrobial activity of HM-242, a novel antiseptic compound.\u00a0<\/strong>J. Antibiot.<\/em> 2009<\/strong>, 62<\/em>, 489\u2013493. DOI: 10.1038\/ja.2009.56<\/li>\n
  43. A New Synthetic Method of Zinc(II) Complexes Based on Mixing.\u00a0<\/strong> Yakugaku Zasshi<\/em> 2005<\/strong>, 125<\/em>, 829\u2013832. DOI: 10.1248\/yakushi.125.829<\/li>\n
  44. L-Carnosine and Close Derivatives Accelerate Zinc Uptake from the lntestine in Rats.\u00a0<\/strong> Biomed.Res.Trace.Elements.<\/em> 2001<\/strong>, 12<\/em>, 159\u2013167. ISSN: 1880-1404<\/li>\n
  45. Characterization of Crystalline L-carnosine Zn(II) Complex (Z-103), a Novel Anti-gastric Ulcer Agent: Tautomeric Change of Imidazole Moiety upon Complexation.\u00a0<\/strong>Chem. Pharm. Bull.<\/em> 1990<\/strong>, 38<\/em>, 2140\u20133146. DOI: 10.1248\/cpb.38.3140<\/li>\n
  46. A simple ring-expansion of 1,4-benzothiazines to give 1,5-benzothiazepines.\u00a0<\/strong>J. CHEM. SOC., CHEM. COMMUN.<\/em> 1983<\/strong>, 8<\/em>, 450\u2013451. DOI: 10.1039\/C39830000450<\/li>\n<\/ol>\n<\/div>\n<\/div>\n","protected":false},"excerpt":{"rendered":"

    Hamari’s Past Scientific Publications More publications. The following is a list of historical publications authored by Hamari. Selected List of Published Research The following is a selected list of peer-reviewed research articles authored by Hamari Chemicals, Ltd. Tandem alkylation\u2212second-order asymmetric transformation protocol for the preparation of phenylalanine-type tailor-made \u03b1\u2011amino acids.\u00a0ACS Omega 2018, 3, 9729\u20139737. DOI: 10.1021\/acsomega.8b01424 Second-order asymmetric transformation and its application for the practical synthesis of \u03b1-amino acids. Org. Biomol. Chem. 2018, 16, 4968\u20134972. DOI: 10.1039\/C8OB00963E 2-Pyrrolidinecarboxamide, N-(2-Benzoyl-4-chlorophenyl)-1-[(3,4-dichlorophenyl)methyl]-,(2R)- and (2S)-. e-EROS reagent article. DOI: 10.1002\/047084289X.rn02164 Axially chiral Ni(II) complexes of \u03b1\u2010amino acids: Separation of enantiomers and kinetics of racemization. Chirality 2018, 30, 498\u2013508. DOI: 10.1002\/chir.2281 Identification of novel plasminogen activator inhibitor-1 inhibitors with improved oral bioavailability: Structure optimization of N-acylanthranilic acid derivatives.\u00a0Bioorg. Med. Chem. Lett. 2018, 28, 809\u2013813. DOI: 10.1016\/j.bmcl.2017.11.016 \u5065\u5eb7\u6210\u4eba\u7537\u6027\u306b\u304a\u3051\u308b\u30e2\u30f3\u30c6\u30eb\u30ab\u30b9\u30c8\u30c1\u30e5\u30a2\u30d6\u30eb\u93205 mg\u300cAA\u300d\/\u300c\u30a2\u30b9\u30da\u30f3\u300d\/\u300c\u30aa\u30fc\u30cf\u30e9\u300d\u306e\u751f\u7269\u5b66\u7684\u540c\u7b49\u6027\u8a66\u9a13. \u81e8\u5e8a\u533b\u85ac 2017, 33, 5, 443\u2013468. ISSN: 0910-8211 An N-protection free ligation of the peptide thioester and the peptide with an N-alkoxy- or N-aryloxyamino group at its N-terminus.\u00a0Tetrahedron Lett.\u00a02017,\u00a058, 4638\u20134641. DOI: 10.1016\/j.tetlet.2017.10.074 Analysis of crystallographic structures of Ni(II) complexes of \u03b1-amino acid Schiff bases: Elucidation of the substituent effect on stereochemical preferences.\u00a0Dalton Trans. 2017, 46, 4191\u20134198. DOI: 10.1039\/C7DT00014F Operationally convenient and scalable asymmetric synthesis of (2S)- and (2R)-\u03b1-(methyl)cysteine derivatives through alkylation of chiral alanine schiff base NiII complexes\u00a0Eur. J. Org. Chem. 2017, 14, 1931\u20131939. DOI: 10.1002\/ejoc.201700018 Scale-up synthesis of (R)- and (S)-N-(2-Benzoyl-4-chlorophenyl)-1-(3,4-dichlorobenzyl) pyrrolidine-2-carboxamide hydrochloride, a versatile reagent for the preparation of tailor-made \u03b1- and \u03b2-amino acids in an enantiomerically pure form. Org. Process Res. Dev. 2017, 21, 732\u2013739. DOI: 10.1021\/acs.oprd.7b00055 Recent approaches for asymmetric synthesis of \u03b1-amino acids via homologation of Ni(II) complexes.\u00a0Amino Acids 2017, 49, 1487\u20131520. DOI: 10.1007\/s00726-017-2458-6 Asymmetric synthesis of \u03b1-deuterated \u03b1-amino acids.\u00a0Org. Biomol. Chem. 2017, 15, 6978\u20136983. DOI: 10.1039\/C7OB01720K Unprecedented property of 4,6-di(substituted)amino-1,2-dihydro-1,3,5-triazines: Formation of acid salts by simple treatment with alkali metal salts of[…Continue Reading]<\/a><\/p>\n","protected":false},"author":4,"featured_media":0,"parent":1792,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"page-technology.php","meta":{"footnotes":""},"class_list":["post-4050","page","type-page","status-publish","hentry"],"yoast_head":"\nHistorical Publications - Hamari Chemicals, Ltd.<\/title>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/www.hamarichemicals.com\/eng\/technology\/publication-list\/hamari-historical-publication-list\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Historical Publications - Hamari Chemicals, Ltd.\" \/>\n<meta property=\"og:description\" content=\"Hamari’s Past Scientific Publications More publications. The following is a list of historical publications authored by Hamari. Selected List of Published Research The following is a selected list of peer-reviewed research articles authored by Hamari Chemicals, Ltd. Tandem alkylation\u2212second-order asymmetric transformation protocol for the preparation of phenylalanine-type tailor-made \u03b1\u2011amino acids.\u00a0ACS Omega 2018, 3, 9729\u20139737. DOI: 10.1021\/acsomega.8b01424 Second-order asymmetric transformation and its application for the practical synthesis of \u03b1-amino acids. Org. Biomol. Chem. 2018, 16, 4968\u20134972. DOI: 10.1039\/C8OB00963E 2-Pyrrolidinecarboxamide, N-(2-Benzoyl-4-chlorophenyl)-1-[(3,4-dichlorophenyl)methyl]-,(2R)- and (2S)-. e-EROS reagent article. DOI: 10.1002\/047084289X.rn02164 Axially chiral Ni(II) complexes of \u03b1\u2010amino acids: Separation of enantiomers and kinetics of racemization. Chirality 2018, 30, 498\u2013508. DOI: 10.1002\/chir.2281 Identification of novel plasminogen activator inhibitor-1 inhibitors with improved oral bioavailability: Structure optimization of N-acylanthranilic acid derivatives.\u00a0Bioorg. Med. Chem. Lett. 2018, 28, 809\u2013813. DOI: 10.1016\/j.bmcl.2017.11.016 \u5065\u5eb7\u6210\u4eba\u7537\u6027\u306b\u304a\u3051\u308b\u30e2\u30f3\u30c6\u30eb\u30ab\u30b9\u30c8\u30c1\u30e5\u30a2\u30d6\u30eb\u93205 mg\u300cAA\u300d\/\u300c\u30a2\u30b9\u30da\u30f3\u300d\/\u300c\u30aa\u30fc\u30cf\u30e9\u300d\u306e\u751f\u7269\u5b66\u7684\u540c\u7b49\u6027\u8a66\u9a13. \u81e8\u5e8a\u533b\u85ac 2017, 33, 5, 443\u2013468. ISSN: 0910-8211 An N-protection free ligation of the peptide thioester and the peptide with an N-alkoxy- or N-aryloxyamino group at its N-terminus.\u00a0Tetrahedron Lett.\u00a02017,\u00a058, 4638\u20134641. DOI: 10.1016\/j.tetlet.2017.10.074 Analysis of crystallographic structures of Ni(II) complexes of \u03b1-amino acid Schiff bases: Elucidation of the substituent effect on stereochemical preferences.\u00a0Dalton Trans. 2017, 46, 4191\u20134198. DOI: 10.1039\/C7DT00014F Operationally convenient and scalable asymmetric synthesis of (2S)- and (2R)-\u03b1-(methyl)cysteine derivatives through alkylation of chiral alanine schiff base NiII complexes\u00a0Eur. J. Org. Chem. 2017, 14, 1931\u20131939. DOI: 10.1002\/ejoc.201700018 Scale-up synthesis of (R)- and (S)-N-(2-Benzoyl-4-chlorophenyl)-1-(3,4-dichlorobenzyl) pyrrolidine-2-carboxamide hydrochloride, a versatile reagent for the preparation of tailor-made \u03b1- and \u03b2-amino acids in an enantiomerically pure form. Org. Process Res. Dev. 2017, 21, 732\u2013739. DOI: 10.1021\/acs.oprd.7b00055 Recent approaches for asymmetric synthesis of \u03b1-amino acids via homologation of Ni(II) complexes.\u00a0Amino Acids 2017, 49, 1487\u20131520. DOI: 10.1007\/s00726-017-2458-6 Asymmetric synthesis of \u03b1-deuterated \u03b1-amino acids.\u00a0Org. Biomol. Chem. 2017, 15, 6978\u20136983. DOI: 10.1039\/C7OB01720K Unprecedented property of 4,6-di(substituted)amino-1,2-dihydro-1,3,5-triazines: Formation of acid salts by simple treatment with alkali metal salts of[...Continue Reading]\" \/>\n<meta property=\"og:url\" content=\"https:\/\/www.hamarichemicals.com\/eng\/technology\/publication-list\/hamari-historical-publication-list\/\" \/>\n<meta property=\"og:site_name\" content=\"Hamari Chemicals, Ltd.\" \/>\n<meta property=\"article:modified_time\" content=\"2022-01-26T05:06:16+00:00\" \/>\n<meta name=\"twitter:card\" content=\"summary_large_image\" \/>\n<meta name=\"twitter:label1\" content=\"Est. reading time\" \/>\n\t<meta name=\"twitter:data1\" content=\"5 minutes\" \/>\n<script type=\"application\/ld+json\" class=\"yoast-schema-graph\">{\"@context\":\"https:\/\/schema.org\",\"@graph\":[{\"@type\":\"WebPage\",\"@id\":\"https:\/\/www.hamarichemicals.com\/eng\/technology\/publication-list\/hamari-historical-publication-list\/\",\"url\":\"https:\/\/www.hamarichemicals.com\/eng\/technology\/publication-list\/hamari-historical-publication-list\/\",\"name\":\"Historical Publications - Hamari Chemicals, Ltd.\",\"isPartOf\":{\"@id\":\"https:\/\/www.hamarichemicals.com\/eng\/#website\"},\"datePublished\":\"2020-09-30T06:25:19+00:00\",\"dateModified\":\"2022-01-26T05:06:16+00:00\",\"breadcrumb\":{\"@id\":\"https:\/\/www.hamarichemicals.com\/eng\/technology\/publication-list\/hamari-historical-publication-list\/#breadcrumb\"},\"inLanguage\":\"en-US\",\"potentialAction\":[{\"@type\":\"ReadAction\",\"target\":[\"https:\/\/www.hamarichemicals.com\/eng\/technology\/publication-list\/hamari-historical-publication-list\/\"]}]},{\"@type\":\"BreadcrumbList\",\"@id\":\"https:\/\/www.hamarichemicals.com\/eng\/technology\/publication-list\/hamari-historical-publication-list\/#breadcrumb\",\"itemListElement\":[{\"@type\":\"ListItem\",\"position\":1,\"name\":\"\u30db\u30fc\u30e0\",\"item\":\"https:\/\/www.hamarichemicals.com\/eng\/\"},{\"@type\":\"ListItem\",\"position\":2,\"name\":\"Technology\",\"item\":\"https:\/\/www.hamarichemicals.com\/eng\/technology\/\"},{\"@type\":\"ListItem\",\"position\":3,\"name\":\"Scientific Publications\",\"item\":\"https:\/\/www.hamarichemicals.com\/eng\/technology\/publication-list\/\"},{\"@type\":\"ListItem\",\"position\":4,\"name\":\"Historical Publications\"}]},{\"@type\":\"WebSite\",\"@id\":\"https:\/\/www.hamarichemicals.com\/eng\/#website\",\"url\":\"https:\/\/www.hamarichemicals.com\/eng\/\",\"name\":\"Hamari Chemicals, Ltd.\",\"description\":\"Hamari Chemicals, Ltd.'s Website\",\"potentialAction\":[{\"@type\":\"SearchAction\",\"target\":{\"@type\":\"EntryPoint\",\"urlTemplate\":\"https:\/\/www.hamarichemicals.com\/eng\/?s={search_term_string}\"},\"query-input\":{\"@type\":\"PropertyValueSpecification\",\"valueRequired\":true,\"valueName\":\"search_term_string\"}}],\"inLanguage\":\"en-US\"}]}<\/script>\n<!-- \/ Yoast SEO plugin. -->","yoast_head_json":{"title":"Historical Publications - Hamari Chemicals, Ltd.","robots":{"index":"index","follow":"follow","max-snippet":"max-snippet:-1","max-image-preview":"max-image-preview:large","max-video-preview":"max-video-preview:-1"},"canonical":"https:\/\/www.hamarichemicals.com\/eng\/technology\/publication-list\/hamari-historical-publication-list\/","og_locale":"en_US","og_type":"article","og_title":"Historical Publications - Hamari Chemicals, Ltd.","og_description":"Hamari’s Past Scientific Publications More publications. The following is a list of historical publications authored by Hamari. Selected List of Published Research The following is a selected list of peer-reviewed research articles authored by Hamari Chemicals, Ltd. Tandem alkylation\u2212second-order asymmetric transformation protocol for the preparation of phenylalanine-type tailor-made \u03b1\u2011amino acids.\u00a0ACS Omega 2018, 3, 9729\u20139737. DOI: 10.1021\/acsomega.8b01424 Second-order asymmetric transformation and its application for the practical synthesis of \u03b1-amino acids. Org. Biomol. Chem. 2018, 16, 4968\u20134972. DOI: 10.1039\/C8OB00963E 2-Pyrrolidinecarboxamide, N-(2-Benzoyl-4-chlorophenyl)-1-[(3,4-dichlorophenyl)methyl]-,(2R)- and (2S)-. e-EROS reagent article. DOI: 10.1002\/047084289X.rn02164 Axially chiral Ni(II) complexes of \u03b1\u2010amino acids: Separation of enantiomers and kinetics of racemization. Chirality 2018, 30, 498\u2013508. DOI: 10.1002\/chir.2281 Identification of novel plasminogen activator inhibitor-1 inhibitors with improved oral bioavailability: Structure optimization of N-acylanthranilic acid derivatives.\u00a0Bioorg. Med. Chem. Lett. 2018, 28, 809\u2013813. DOI: 10.1016\/j.bmcl.2017.11.016 \u5065\u5eb7\u6210\u4eba\u7537\u6027\u306b\u304a\u3051\u308b\u30e2\u30f3\u30c6\u30eb\u30ab\u30b9\u30c8\u30c1\u30e5\u30a2\u30d6\u30eb\u93205 mg\u300cAA\u300d\/\u300c\u30a2\u30b9\u30da\u30f3\u300d\/\u300c\u30aa\u30fc\u30cf\u30e9\u300d\u306e\u751f\u7269\u5b66\u7684\u540c\u7b49\u6027\u8a66\u9a13. \u81e8\u5e8a\u533b\u85ac 2017, 33, 5, 443\u2013468. ISSN: 0910-8211 An N-protection free ligation of the peptide thioester and the peptide with an N-alkoxy- or N-aryloxyamino group at its N-terminus.\u00a0Tetrahedron Lett.\u00a02017,\u00a058, 4638\u20134641. DOI: 10.1016\/j.tetlet.2017.10.074 Analysis of crystallographic structures of Ni(II) complexes of \u03b1-amino acid Schiff bases: Elucidation of the substituent effect on stereochemical preferences.\u00a0Dalton Trans. 2017, 46, 4191\u20134198. DOI: 10.1039\/C7DT00014F Operationally convenient and scalable asymmetric synthesis of (2S)- and (2R)-\u03b1-(methyl)cysteine derivatives through alkylation of chiral alanine schiff base NiII complexes\u00a0Eur. J. Org. Chem. 2017, 14, 1931\u20131939. DOI: 10.1002\/ejoc.201700018 Scale-up synthesis of (R)- and (S)-N-(2-Benzoyl-4-chlorophenyl)-1-(3,4-dichlorobenzyl) pyrrolidine-2-carboxamide hydrochloride, a versatile reagent for the preparation of tailor-made \u03b1- and \u03b2-amino acids in an enantiomerically pure form. Org. Process Res. Dev. 2017, 21, 732\u2013739. DOI: 10.1021\/acs.oprd.7b00055 Recent approaches for asymmetric synthesis of \u03b1-amino acids via homologation of Ni(II) complexes.\u00a0Amino Acids 2017, 49, 1487\u20131520. DOI: 10.1007\/s00726-017-2458-6 Asymmetric synthesis of \u03b1-deuterated \u03b1-amino acids.\u00a0Org. Biomol. Chem. 2017, 15, 6978\u20136983. DOI: 10.1039\/C7OB01720K Unprecedented property of 4,6-di(substituted)amino-1,2-dihydro-1,3,5-triazines: Formation of acid salts by simple treatment with alkali metal salts of[...Continue Reading]","og_url":"https:\/\/www.hamarichemicals.com\/eng\/technology\/publication-list\/hamari-historical-publication-list\/","og_site_name":"Hamari Chemicals, Ltd.","article_modified_time":"2022-01-26T05:06:16+00:00","twitter_card":"summary_large_image","twitter_misc":{"Est. reading time":"5 minutes"},"schema":{"@context":"https:\/\/schema.org","@graph":[{"@type":"WebPage","@id":"https:\/\/www.hamarichemicals.com\/eng\/technology\/publication-list\/hamari-historical-publication-list\/","url":"https:\/\/www.hamarichemicals.com\/eng\/technology\/publication-list\/hamari-historical-publication-list\/","name":"Historical Publications - Hamari Chemicals, Ltd.","isPartOf":{"@id":"https:\/\/www.hamarichemicals.com\/eng\/#website"},"datePublished":"2020-09-30T06:25:19+00:00","dateModified":"2022-01-26T05:06:16+00:00","breadcrumb":{"@id":"https:\/\/www.hamarichemicals.com\/eng\/technology\/publication-list\/hamari-historical-publication-list\/#breadcrumb"},"inLanguage":"en-US","potentialAction":[{"@type":"ReadAction","target":["https:\/\/www.hamarichemicals.com\/eng\/technology\/publication-list\/hamari-historical-publication-list\/"]}]},{"@type":"BreadcrumbList","@id":"https:\/\/www.hamarichemicals.com\/eng\/technology\/publication-list\/hamari-historical-publication-list\/#breadcrumb","itemListElement":[{"@type":"ListItem","position":1,"name":"\u30db\u30fc\u30e0","item":"https:\/\/www.hamarichemicals.com\/eng\/"},{"@type":"ListItem","position":2,"name":"Technology","item":"https:\/\/www.hamarichemicals.com\/eng\/technology\/"},{"@type":"ListItem","position":3,"name":"Scientific Publications","item":"https:\/\/www.hamarichemicals.com\/eng\/technology\/publication-list\/"},{"@type":"ListItem","position":4,"name":"Historical Publications"}]},{"@type":"WebSite","@id":"https:\/\/www.hamarichemicals.com\/eng\/#website","url":"https:\/\/www.hamarichemicals.com\/eng\/","name":"Hamari Chemicals, Ltd.","description":"Hamari Chemicals, Ltd.'s Website","potentialAction":[{"@type":"SearchAction","target":{"@type":"EntryPoint","urlTemplate":"https:\/\/www.hamarichemicals.com\/eng\/?s={search_term_string}"},"query-input":{"@type":"PropertyValueSpecification","valueRequired":true,"valueName":"search_term_string"}}],"inLanguage":"en-US"}]}},"jetpack_shortlink":"https:\/\/wp.me\/P9dlmH-13k","_links":{"self":[{"href":"https:\/\/www.hamarichemicals.com\/eng\/wp-json\/wp\/v2\/pages\/4050","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/www.hamarichemicals.com\/eng\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/www.hamarichemicals.com\/eng\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/www.hamarichemicals.com\/eng\/wp-json\/wp\/v2\/users\/4"}],"replies":[{"embeddable":true,"href":"https:\/\/www.hamarichemicals.com\/eng\/wp-json\/wp\/v2\/comments?post=4050"}],"version-history":[{"count":20,"href":"https:\/\/www.hamarichemicals.com\/eng\/wp-json\/wp\/v2\/pages\/4050\/revisions"}],"predecessor-version":[{"id":9210,"href":"https:\/\/www.hamarichemicals.com\/eng\/wp-json\/wp\/v2\/pages\/4050\/revisions\/9210"}],"up":[{"embeddable":true,"href":"https:\/\/www.hamarichemicals.com\/eng\/wp-json\/wp\/v2\/pages\/1792"}],"wp:attachment":[{"href":"https:\/\/www.hamarichemicals.com\/eng\/wp-json\/wp\/v2\/media?parent=4050"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}