Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Teyrnon C. Jones"'
Autor:
Teyrnon C. Jones, Collette S. Guy
Publikováno v:
Synlett. 2009:2253-2256
A mild, ligand-free method of arylating 2,4-quinazolinediones Using arylboronates in the presence of copper salts is described. The reaction is tolerant of a variety of functional groups and works for arylboronic acid, arylboronic ester, and aryltrif
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ce84fda58a72888431e5260ffb6bd5cd
https://doi.org/10.1055/s-0029-1217724
https://doi.org/10.1055/s-0029-1217724
Autor:
George J. Ellames, Catherine Noban, Teyrnon C. Jones, Alan C. Spivey, Andrew D. Kohler, Laetitia J. Martin
Publikováno v:
Journal of Labelled Compounds and Radiopharmaceuticals. 50:281-285
Strategies for the use of germanium-based linkers for the phase-tagged synthesis of isotopically labelled intermediates are described. Protocols of potential use in the devolatilization of volatile intermediates prepared from [ 14 C]-CO 2 and [ 14 C]
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::841a3782d76028af988f0b08e52754e7
https://doi.org/10.1002/jlcr.1302
https://doi.org/10.1002/jlcr.1302
Autor:
Kerri L. Jones, Adrian Hall, Paul H. Taylor, Teyrnon C. Jones, Nicholas C. O. Tomkinson, Robert Poerzig, Sze Chak Yau, Niall M. Killeen
Publikováno v:
Synlett. 2006:3435-3438
The first method for the direct formation of α-oxycarbonates from both aldehydes and ketones is described. N-Methyl-O-alkoxyformate hydroxylamine hydrochloride reagents can be prepd. in two high-yielding steps from N-Boc-N-methylhydroxylamine and we
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::677a68e39803eedd5e4518a656c399c2
https://doi.org/10.1055/s-2006-956473
https://doi.org/10.1055/s-2006-956473
A method for the parallel solid-phase synthesis (SPS) of iodinated analogues of Sanofi-Aventis' type 1 cannabinoid (CB1) receptor inverse agonist rimonabant (acomplia) has been developed. The method allows the synthesis of a range of C3 amide/hydrazi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dbd49165106877fecdba78923ce1a10b
http://hdl.handle.net/10044/1/15223
http://hdl.handle.net/10044/1/15223
Publikováno v:
Organic Syntheses
A convenient method for the prepn. of α-acyloxy ketones is described. Oxyacylation of a variety of ketones with O-acyl hydroxyamine derivs. provided the corresponding α-acyloxy ketones in good yields. (2-Benzoyloxy)-1,4-cyclohexanedione mono-ethyle
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0b8f79aab69f192cc42aa4665bbd9702
https://doi.org/10.1002/0471264229.os084.24
https://doi.org/10.1002/0471264229.os084.24
Autor:
Kerri L. Jones, Nicholas C. O. Tomkinson, Adrian Hall, Sze Chak Yau, Niall M. Killeen, Teyrnon C. Jones, Edouard P. Huguet
Publikováno v:
ChemInform. 38
A simple one-pot method for the direct introduction of carbamates α to carbonyl groups that proceeds at room temp. in the presence of both moisture and air was developed. Treatment of aldehydes and both cyclic and acyclic ketones with N-methyl-O-car
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4fbafad8ab65971cecfe0c308da823e2
https://doi.org/10.1002/chin.200724085
https://doi.org/10.1002/chin.200724085
Autor:
Niall M. Killeen, Teyrnon C. Jones, Nicholas C. O. Tomkinson, Adrian Hall, Paul H. Taylor, Kerri L. Jones, Cory S. Beshara, Robert J. Jenkins, Stephen P. Thomas
Publikováno v:
Organic letters. 7(25)
[chemical reaction: see text]. A simple, one-pot method for the alpha-acyloxylation of carbonyl compounds that proceeds at room temperature in the presence of both moisture and air has been developed. Treatment of a variety of aldehydes and both cycl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::99f783468963e844d75a7047094daeac
https://pubmed.ncbi.nlm.nih.gov/16321033
https://pubmed.ncbi.nlm.nih.gov/16321033
Autor:
Stephen P. Thomas, Nicholas C. O. Tomkinson, Cory S. Beshara, Teyrnon C. Jones, Adrian Hall, Rachael T. Parry, Robert Leyshon Jenkins
Publikováno v:
ChemInform. 36
A mild, efficient and general method for the chemospecific alpha-oxygenation of aldehydes is described. Treatment of a series of aldehydes with N-tert-butyl-O-benzoyl hydroxylamine hydrochloride gives the corresponding alpha-oxygenated carbonyl via a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d13d65ac1d5bd93cf008886159e6a28f
https://doi.org/10.1002/chin.200533056
https://doi.org/10.1002/chin.200533056
Publikováno v:
Synfacts. 2010:0115-0115
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6368b4fe56884d34bf43b2754925a340
https://doi.org/10.1055/s-0029-1218442
https://doi.org/10.1055/s-0029-1218442
Publikováno v:
Organic Letters; Oct2009, Vol. 11 Issue 20, p4760-4763, 4p