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<SDOBI lang="en"><B000><eptags><B001EP>ATBECHDEDKESFRGBGRITLILUNLSEMCPTIESILTLVFIROMKCYALTRBGCZEEHUPLSK..HRIS..MTNORS..SM..................</B001EP><B003EP>*</B003EP><B005EP>J</B005EP><B007EP>BDM Ver 2.0.16 (1th of February 2022) -  2999001/0</B007EP></eptags></B000><B100><B110>3749635</B110><B120><B121>CORRECTED EUROPEAN PATENT SPECIFICATION</B121></B120><B130>B8</B130><B132EP>B1</B132EP><B140><date>20220817</date></B140><B150><B151>W1</B151><B153>73</B153><B155><B1551>de</B1551><B1552>Bibliographie</B1552><B1551>en</B1551><B1552>Bibliography</B1552><B1551>fr</B1551><B1552>Bibliographie</B1552></B155></B150><B190>EP</B190></B100><B200><B210>19703019.0</B210><B220><date>20190123</date></B220><B240><B241><date>20200701</date></B241><B242><date>20210722</date></B242></B240><B250>en</B250><B251EP>en</B251EP><B260>en</B260></B200><B300><B310>PA201800064</B310><B320><date>20180209</date></B320><B330><ctry>DK</ctry></B330></B300><B400><B405><date>20220817</date><bnum>202233</bnum></B405><B430><date>20201216</date><bnum>202051</bnum></B430><B450><date>20220713</date><bnum>202228</bnum></B450><B452EP><date>20220309</date></B452EP><B480><date>20220817</date><bnum>202233</bnum></B480></B400><B500><B510EP><classification-ipcr sequence="1"><text>C07C  67/39        20060101AFI20190816BHEP        </text></classification-ipcr><classification-ipcr sequence="2"><text>C07C  69/675       20060101ALI20190816BHEP        </text></classification-ipcr><classification-ipcr sequence="3"><text>C07C  51/16        20060101ALI20190816BHEP        </text></classification-ipcr><classification-ipcr sequence="4"><text>C07C  69/732       20060101ALI20190816BHEP        </text></classification-ipcr><classification-ipcr sequence="5"><text>C07C  59/105       20060101ALI20190816BHEP        </text></classification-ipcr><classification-ipcr sequence="6"><text>C07C  59/48        20060101ALI20190816BHEP        </text></classification-ipcr></B510EP><B520EP><classifications-cset><classification-cset group-number="1"><classification-cpc rank="1"><text>C07C  67/39        20130101 LI20190408BHEP        </text></classification-cpc><classification-cpc rank="2"><text>C07C  69/675       20130101 LI20190408BHEP        </text></classification-cpc></classification-cset><classification-cset group-number="2"><classification-cpc rank="1"><text>C07C  67/39        20130101 LI20190408BHEP        </text></classification-cpc><classification-cpc rank="2"><text>C07C  69/732       20130101 LI20190408BHEP        </text></classification-cpc></classification-cset><classification-cset group-number="3"><classification-cpc rank="1"><text>C07C  51/16        20130101 LI20190408BHEP        </text></classification-cpc><classification-cpc rank="2"><text>C07C  59/105       20130101 LI20190408BHEP        </text></classification-cpc></classification-cset><classification-cset group-number="4"><classification-cpc rank="1"><text>C07C  51/16        20130101 LI20190408BHEP        </text></classification-cpc><classification-cpc rank="2"><text>C07C  59/48        20130101 LI20190408BHEP        </text></classification-cpc></classification-cset></classifications-cset><classifications-cpc><classification-cpc sequence="1"><text>C07C  67/39        20130101 FI20190408BHEP        </text></classification-cpc><classification-cpc sequence="2"><text>C07C  51/16        20130101 LI20190408BHEP        </text></classification-cpc><classification-cpc sequence="3"><text>B01J  29/7057      20130101 LI20190916BHEP        </text></classification-cpc></classifications-cpc></B520EP><B540><B541>de</B541><B542>VERFAHREN ZUR HERSTELLUNG VON ALPHA-HYDROXY-VERBINDUNGEN UND VERWENDUNGEN DAVON</B542><B541>en</B541><B542>PROCESS OF PRODUCING ALPHA-HYDROXY COMPOUNDS AND USES THEREOF</B542><B541>fr</B541><B542>PROCÉDÉ DE PRODUCTION DE COMPOSÉS ALPHA-HYDROXY ET LEURS UTILISATIONS</B542></B540><B560><B561><text>EP-A1- 0 245 231</text></B561><B561><text>WO-A1-2016/174231</text></B561><B561><text>US-A1- 2017 015 614</text></B561><B561><text>US-A1- 2017 369 434</text></B561><B562><text>VAN DER HEIJDEN, G ET AL.: "Metal-free one pot alpha-carboxylation of primary alcohols.", ORGANIC &amp; BIOMOLECULAR CHEMISTRY, vol. 14, no. 41, 1 July 2016 (2016-07-01), pages 9716-9719,</text></B562><B562><text>VERARDO, G ET AL.: "Exploring the reaction of iodine with alpha-diazo esters.", JOURNAL OF PHYSICAL ORGANIC CHEMISTRY, vol. 22, no. 1, 1 July 2016 (2016-07-01), - 1 July 2016 (2016-07-01), pages 24-30,</text></B562><B562><text>NGUYEN S T ET AL: "A concise, total synthesis and antibacterial evaluation of 2-hydroxy-1-(1H-indol-3-yl)-4-methylpentan -3-one", BIOORGANIC &amp; MEDICINAL CHEMISTRY LETTERS, ELSEVIER, AMSTERDAM, NL, vol. 20, no. 19, 1 October 2010 (2010-10-01), pages 5739-5742, XP027273552, ISSN: 0960-894X [retrieved on 2010-09-08]</text></B562><B562><text>GAO, S ET AL.: SYNLETT, vol. 27, no. 11, 8 July 2016 (2016-07-08), - 8 July 2016 (2016-07-08), pages 1748-1752,</text></B562><B562><text>POTERALA, M. ET AL.: "synthesis of new chiral ionic liquids from alpha-hydroxycarboxylic acids.", TETRAHEDRON: ASYMMETRY, vol. 22, no. 3, 1 July 2016 (2016-07-01), pages 294-299,</text></B562><B562><text>BALDRIDGE, R.: "Metabolism of histidine. III. Urinary metabolites.", JOURNAL OF BIOLOGICAL SCIENCE, vol. 233, 9 July 2016 (2016-07-09), pages 125-127,</text></B562></B560></B500><B700><B720><B721><snm>TAARNING, Esben</snm><adr><str>Smallegade 24, 3th</str><city>2000 Frederiksberg</city><ctry>DK</ctry></adr></B721><B721><snm>TOLBORG, Søren</snm><adr><str>Furesøgårdsvej 12</str><city>3520 Farum</city><ctry>DK</ctry></adr></B721><B721><snm>MARTÍNEZ ESPÍN, Juan Salvador</snm><adr><str>Næstvedgade 6A. 3th.</str><city>2100 Copenhagen</city><ctry>DK</ctry></adr></B721></B720><B730><B731><snm>Topsoe A/S</snm><iid>101948556</iid><irf>02411-EP</irf><adr><str>Haldor Topsøes Allé 1</str><city>2800 Kgs. 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