{"version":"1.0","provider_name":"Hamari Chemicals, Ltd.","provider_url":"https:\/\/www.hamarichemicals.com\/eng","author_name":"grab8do","author_url":"https:\/\/www.hamarichemicals.com\/eng\/blog\/author\/grab8do\/","title":"Historical Publications - Hamari Chemicals, Ltd.","type":"rich","width":600,"height":338,"html":"<blockquote class=\"wp-embedded-content\" data-secret=\"NcDRFJ7I9v\"><a href=\"https:\/\/www.hamarichemicals.com\/eng\/technology\/publication-list\/hamari-historical-publication-list\/\">Historical Publications<\/a><\/blockquote><iframe sandbox=\"allow-scripts\" security=\"restricted\" src=\"https:\/\/www.hamarichemicals.com\/eng\/technology\/publication-list\/hamari-historical-publication-list\/embed\/#?secret=NcDRFJ7I9v\" width=\"600\" height=\"338\" title=\"&#8220;Historical Publications&#8221; &#8212; Hamari Chemicals, Ltd.\" data-secret=\"NcDRFJ7I9v\" frameborder=\"0\" marginwidth=\"0\" marginheight=\"0\" scrolling=\"no\" class=\"wp-embedded-content\"><\/iframe><script type=\"text\/javascript\">\n\/* <![CDATA[ *\/\n\/*! This file is auto-generated *\/\n!function(d,l){\"use strict\";l.querySelector&&d.addEventListener&&\"undefined\"!=typeof URL&&(d.wp=d.wp||{},d.wp.receiveEmbedMessage||(d.wp.receiveEmbedMessage=function(e){var t=e.data;if((t||t.secret||t.message||t.value)&&!\/[^a-zA-Z0-9]\/.test(t.secret)){for(var s,r,n,a=l.querySelectorAll('iframe[data-secret=\"'+t.secret+'\"]'),o=l.querySelectorAll('blockquote[data-secret=\"'+t.secret+'\"]'),c=new RegExp(\"^https?:$\",\"i\"),i=0;i<o.length;i++)o[i].style.display=\"none\";for(i=0;i<a.length;i++)s=a[i],e.source===s.contentWindow&&(s.removeAttribute(\"style\"),\"height\"===t.message?(1e3<(r=parseInt(t.value,10))?r=1e3:~~r<200&&(r=200),s.height=r):\"link\"===t.message&&(r=new URL(s.getAttribute(\"src\")),n=new URL(t.value),c.test(n.protocol))&&n.host===r.host&&l.activeElement===s&&(d.top.location.href=t.value))}},d.addEventListener(\"message\",d.wp.receiveEmbedMessage,!1),l.addEventListener(\"DOMContentLoaded\",function(){for(var e,t,s=l.querySelectorAll(\"iframe.wp-embedded-content\"),r=0;r<s.length;r++)(t=(e=s[r]).getAttribute(\"data-secret\"))||(t=Math.random().toString(36).substring(2,12),e.src+=\"#?secret=\"+t,e.setAttribute(\"data-secret\",t)),e.contentWindow.postMessage({message:\"ready\",secret:t},\"*\")},!1)))}(window,document);\n\/\/# sourceURL=https:\/\/www.hamarichemicals.com\/eng\/wp-includes\/js\/wp-embed.min.js\n\/* ]]> *\/\n<\/script>\n","description":"Hamari&#8217;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 [&hellip;]"}