Synlett, Table of Contents LETTER© Georg Thieme Verlag Stuttgart ˙ New YorkDeuterium-labeled 2′-HydroxypyridoxolNisar Ullah, Johannes Zeidler, Ian D. Spenser*Department of Chemistry, McMaster University, Hamilton, Ontario L8S 4M1, CanadaFax: +1(905)5222509; e-Mail: spenser@mcmaster.ca; Recommend Article Abstract Buy Article All articles of this category Abstract The preparation of [5′,5′-2H2]- and [2′,2′,5′,5′-2H4]-2′-hydroxypyridoxol, as well as of [5′,5′-2H2]-4-pyridoxic acid, starting from 3,4′-O-isopropylidenepyridoxol, is described. The labeled compounds were employed in an investigation of the biosynthesis of Vitamins B1 and B6. Key words deuterium-labeling - vitamins B1 and B6 - biosynthesis - 2′-hydroxypyridoxine - deuterium NMR Full Text References References <A NAME="RS07002ST-1">1</A> Zeidler J. Ullah N. Gupta RN. Pauloski RM. Sayer BG. Spenser ID. J. Am. Chem. Soc. 2002, 124: 4542 <A NAME="RS07002ST-2">2</A> Wu Y. Ahlberg P. Acta Chem. Scand. 1989, 43: 1009 <A NAME="RS07002ST-3">3</A> Nelson JT. Nelson PH. Magn. Reson. Chem. 1987, 25: 309 <A NAME="RS07002ST-4">4</A> Korytnyk W. Wiedeman W. J. Chem. Soc. 1962, 2531 <A NAME="RS07002ST-5">5</A> Iwata M. Kuzuhara H. Bull. Chem. Soc. Jpn. 1985, 58: 2502 <A NAME="RS07002ST-6">6</A> Korytnyk W. Paul B. J. Heterocycl. Chem. 1965, 2: 144 <A NAME="RS07002ST-7">7</A> Korytnyk W. Kris EJ. Singh RP. J. Org. Chem. 1964, 29: 574 <A NAME="RS07002ST-8">8</A> Argoudelis CJ. Kummerow FA. J. Org. Chem. 1964, 29: 2663 <A NAME="RS07002ST-9">9</A> Tomita I. Brooks HG. Metzler DE. J. Heterocycl. Chem. 1966, 3: 178 <A NAME="RS07002ST-10">10</A> Tazuya K. Azumi C. Yamada K. Kumaoka H. Vitamins (Japan) 1995, 69: 167 <A NAME="RS07002ST-11">11</A> Coburn SP. Lin CC. Schaltenbrand WE. Mahuren JD. J. Labelled Compd. Radiopharm. 1982, 19: 703 <A NAME="RS07002ST-12">12</A> Korytnyk W. Paul B. J. Heterocycl. Chem. 1965, 2: 481 <A NAME="RS07002ST-13">13</A> Ahrens H. Korytnyk W. J. Heterocycl. Chem. 1967, 4: 625 <A NAME="RS07002ST-14">14</A> Huff JW. Perlzweig WA. J. Biol. Chem. 1944, 155: 345 <A NAME="RS07002ST-15">15</A> Korytnyk W. Srivastava SC. Angelino N. Potti PGG. Paul B. J. Med. Chem. 1973, 16: 1096 <A NAME="RS07002ST-16">16</A> Agrawal KC. Clayman S. Sartorelli AC. J. Pharm. Sci. 1976, 65: 297 <A NAME="RS07002ST-17">17</A> Bedford GR. Katritzky AR. Wuest HM. J. Chem. Soc. 1963, 4600