Dergi makalesi Açık Erişim
Kayan, Cezmi; Meric, Nermin; Rafikova, Khadichakhan; Zazybin, Alexey; Gurbuz, Nevin; Karakaplan, Mehmet; Aydemir, Murat
<?xml version='1.0' encoding='UTF-8'?> <record xmlns="http://www.loc.gov/MARC21/slim"> <leader>00000nam##2200000uu#4500</leader> <datafield tag="700" ind1=" " ind2=" "> <subfield code="a">Meric, Nermin</subfield> <subfield code="u">Dicle Univ, Fac Sci, Dept Chem, TR-21280 Diyarbakir, Turkey</subfield> </datafield> <datafield tag="700" ind1=" " ind2=" "> <subfield code="a">Rafikova, Khadichakhan</subfield> </datafield> <datafield tag="700" ind1=" " ind2=" "> <subfield code="a">Zazybin, Alexey</subfield> </datafield> <datafield tag="700" ind1=" " ind2=" "> <subfield code="a">Gurbuz, Nevin</subfield> <subfield code="u">Univ Inonu, Fac Sci, Dept Chem, TR-44280 Malatya, Turkey</subfield> </datafield> <datafield tag="700" ind1=" " ind2=" "> <subfield code="a">Karakaplan, Mehmet</subfield> <subfield code="u">Dicle Univ, Fac Sci, Dept Chem, TR-21280 Diyarbakir, Turkey</subfield> </datafield> <datafield tag="700" ind1=" " ind2=" "> <subfield code="a">Aydemir, Murat</subfield> <subfield code="u">Dicle Univ, Fac Sci, Dept Chem, TR-21280 Diyarbakir, Turkey</subfield> </datafield> <datafield tag="909" ind1="C" ind2="4"> <subfield code="c">37-47</subfield> <subfield code="p">JOURNAL OF ORGANOMETALLIC CHEMISTRY</subfield> <subfield code="v">869</subfield> </datafield> <datafield tag="980" ind1=" " ind2=" "> <subfield code="a">user-tubitak-destekli-proje-yayinlari</subfield> </datafield> <datafield tag="540" ind1=" " ind2=" "> <subfield code="a">Creative Commons Attribution</subfield> <subfield code="u">http://www.opendefinition.org/licenses/cc-by</subfield> </datafield> <datafield tag="024" ind1=" " ind2=" "> <subfield code="a">10.1016/j.jorganchem.2018.06.002</subfield> <subfield code="2">doi</subfield> </datafield> <datafield tag="245" ind1=" " ind2=" "> <subfield code="a">A new class of well-defined ruthenium catalysts for enantioselective transfer hydrogenation of various ketones</subfield> </datafield> <datafield tag="100" ind1=" " ind2=" "> <subfield code="a">Kayan, Cezmi</subfield> <subfield code="u">Dicle Univ, Fac Sci, Dept Chem, TR-21280 Diyarbakir, Turkey</subfield> </datafield> <datafield tag="909" ind1="C" ind2="O"> <subfield code="o">oai:zenodo.org:31263</subfield> <subfield code="p">user-tubitak-destekli-proje-yayinlari</subfield> </datafield> <datafield tag="650" ind1="1" ind2="7"> <subfield code="2">opendefinition.org</subfield> <subfield code="a">cc-by</subfield> </datafield> <datafield tag="260" ind1=" " ind2=" "> <subfield code="c">2018-01-01</subfield> </datafield> <datafield tag="856" ind1="4" ind2=" "> <subfield code="u">https://aperta.ulakbim.gov.trrecord/31263/files/bib-2ded0bc1-a74b-480d-97d6-49d57c68e026.txt</subfield> <subfield code="z">md5:d0d5dd27b7216a3985d65339532b0d8d</subfield> <subfield code="s">264</subfield> </datafield> <datafield tag="542" ind1=" " ind2=" "> <subfield code="l">open</subfield> </datafield> <controlfield tag="005">20210315182604.0</controlfield> <controlfield tag="001">31263</controlfield> <datafield tag="980" ind1=" " ind2=" "> <subfield code="a">publication</subfield> <subfield code="b">article</subfield> </datafield> <datafield tag="520" ind1=" " ind2=" "> <subfield code="a">A pair of novel optically pure phosphinite ligands were synthesized by ring opening reaction of chiral amines with (R)-styrene oxide or (S)-glycidyl phenyl ether oxide using a straightforward method in high yields and their ruthenium complexes were described in detail. The ruthenium complexes proved to be highly efficient catalysts for the enantioselective hydrogenation of ketones, affording products up to 99% ee. The results showed that the corresponding chiral alcohols could be obtained with high activity and excellent enantioselectivities at the desired temperature. (2S)-1-{benzyl[(1S)-1-(naphthalen-1-yl)ethyl]amino}-3-phenoxypropan-2-yl diphenylphosphinito[dichloro(eta(6)-benzene)ruthenium (II)] acts an excellent catalyst in the reduction of ketones, giving the corresponding alcohol up to 99% ee. (C) 2018 Elsevier B.V. All rights reserved.</subfield> </datafield> </record>
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