Works by Kitson, Sean L

Results: 9

Nitrilase mediated mild hydrolysis of a carbon‐14 nitrile for the radiosynthesis of 4‐(7‐hydroxycarbamoyl‐[1‐14C‐heptanoyl]‐oxy)‐benzoic acid methyl ester, [14C]‐SHP‐141: A novel class I/II histone deacetylase (HDAC) inhibitor

Published in:

Journal of Labelled Compounds & Radiopharmaceuticals, 2023, v. 66, n. 7/8, p. 172, doi. 10.1002/jlcr.4026

By:

Kitson, Sean L.;
Watters, William;
Moody, Thomas S.;
Chappell, Todd;
Mazitschek, Ralph

Publication type:

Article

Synthesis of carbon‐14–labelled peptides.

Published in:

Journal of Labelled Compounds & Radiopharmaceuticals, 2019, v. 62, n. 11, p. 713, doi. 10.1002/jlcr.3777

By:

Dell'isola, Antonio;
Brown, Rodney T.;
Jones, Stuart;
Kitson, Sean L.;
Moody, Thomas S.;
Syvret, Jason;
Upeandran, Balasubramaniam;
Watters, William H.

Publication type:

Article

Synthesis of isotopically labelled [14C]ZT-1 (Debio-9902), [d3]ZT-1 and (−)-[d3]huperzine A, a new generation of acetylcholinesterase inhibitors.

Published in:

Journal of Labelled Compounds & Radiopharmaceuticals, 2011, v. 54, n. 11, p. 720, doi. 10.1002/jlcr.1918

By:

Leman, Loïc;
Kitson, Sean L;
Brown, Rodney T;
Cairns, Jana;
Watters, William;
McMordie, Austin;
Murrell, Victor L;
Marfurt, Judith

Publication type:

Article

Carbon-14 radiosynthesis of 4-(5-chloro-2-hydroxyphenyl)-3-(2-hydroxyethyl)-6-(trifluoromethyl)-[4-14C]quinolin-2(1 H)-one (XEN-D0401), A novel BK channel activator.

Published in:

Journal of Labelled Compounds & Radiopharmaceuticals, 2010, v. 53, n. 3, p. 140, doi. 10.1002/jlcr.1740

By:

Kitson, Sean L.;
Jones, Stuart;
Watters, William;
Chan, Fiona;
Madge, David

Publication type:

Article

Amersham radiochemistry to GE Healthcare.

Published in:

Journal of Labelled Compounds & Radiopharmaceuticals, 2007, v. 50, n. 9/10, p. 737, doi. 10.1002/jlcr.1427

By:

Kitson, Sean L.

Publication type:

Article

Mechanism of the Bischler-Napieralski exocyclic and endocyclic dehydration products in the radiosynthesis of ( R)-(-)-[6a-14C]apomorphine.

Published in:

Journal of Labelled Compounds & Radiopharmaceuticals, 2007, v. 50, n. 5/6, p. 290, doi. 10.1002/jlcr.1270

By:

Kitson, Sean L.

Publication type:

Article

The design of radiolabeled carbon-14 polymers.

Published in:

Journal of Labelled Compounds & Radiopharmaceuticals, 2007, v. 50, n. 5/6, p. 515, doi. 10.1002/jlcr.1234

By:

Shemilt, Gary;
Newby, Mark;
Kitson, Sean L.

Publication type:

Article

Synthesis of the myoview™ ligand, [bisphosphinoethane-1,2-14C]tetrofosmin.

Published in:

Journal of Labelled Compounds & Radiopharmaceuticals, 2007, v. 50, n. 5/6, p. 468, doi. 10.1002/jlcr.1199

By:

Woolley, Geoffrey T.;
Kitson, Sean L.;
Gordon Reid, R.

Publication type:

Article

Application of the Bischler-Napieralski-Pschorr radiosynthesis of ( R)-(-)-[6a-14C]apomorphine, a non-selective D1/D2 dopamine receptor agonist.

Published in:

Journal of Labelled Compounds & Radiopharmaceuticals, 2006, v. 49, n. 6, p. 517, doi. 10.1002/jlcr.1070

By:

Kitson, Sean L.;
Knagg, Eric

Publication type:

Article

Works by Kitson, Sean L

Nitrilase mediated mild hydrolysis of a carbon‐14 nitrile for the radiosynthesis of 4‐(7‐hydroxycarbamoyl‐[1‐<sup>14</sup>C‐heptanoyl]‐oxy)‐benzoic acid methyl ester, [<sup>14</sup>C]‐SHP‐141: A novel class I/II histone deacetylase (HDAC) inhibitor

Synthesis of carbon‐14–labelled peptides.

Synthesis of isotopically labelled [<sup>14</sup>C]ZT-1 (Debio-9902), [d<sub>3</sub>]ZT-1 and (−)-[d<sub>3</sub>]huperzine A, a new generation of acetylcholinesterase inhibitors.

Carbon-14 radiosynthesis of 4-(5-chloro-2-hydroxyphenyl)-3-(2-hydroxyethyl)-6-(trifluoromethyl)-[4-<sup>14</sup>C]quinolin-2(1 H)-one (XEN-D0401), A novel BK channel activator.

Amersham radiochemistry to GE Healthcare.

Mechanism of the Bischler-Napieralski exocyclic and endocyclic dehydration products in the radiosynthesis of ( R)-(-)-[6a-<sup>14</sup>C]apomorphine.

The design of radiolabeled carbon-14 polymers.

Synthesis of the myoview™ ligand, [bisphosphinoethane-1,2-<sup>14</sup>C]tetrofosmin.

Application of the Bischler-Napieralski-Pschorr radiosynthesis of ( R)-(-)-[6a-<sup>14</sup>C]apomorphine, a non-selective D1/D2 dopamine receptor agonist.