Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Trevor J. Grinter"'
Autor:
and Timothy C. Walsgrove, Clive J. Moores, Richard Neville Saunders, Jerome F. Hayes, Richard J. Atkins, Lynne P. Crawford, Michael Anthony Harris, Christopher Wicks, Gary F. Breen, Trevor J. Grinter, Andrew C. Share
Publikováno v:
Organic Process Research & Development. 1:185-197
The 3,4,8-trisubstituted quinoline derivatives 2-butyryl-8-methoxy-4-[(2-methylphenyl)amino]quinoline and 3-butyryl-8-(2-hydroxyethoxy)-4-[(2-methylphenyl)amino]quinoline were prepared using five novel synthetic strategies, each involving a different
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::71bb87bb1625590969f1c2a8b0464cfc
https://doi.org/10.1021/op9700035
https://doi.org/10.1021/op9700035
Autor:
J. Sydney Davies, Michael Anthony Harris, David J. Merrikin, Richard Keith Anderson, Roger J. Ponsford, Trevor J. Grinter, Carol F. Smith, Christina A. Mitchell, Suzanne C. Cosham, Andrew V. Stachulski, Pauline C. A. Chapman
Publikováno v:
The Journal of Antibiotics. 46:331-342
Syntheses are described for penicillins (4b approximately 4i, 5a and 5b) which possess a 6 beta-(2-heteroaryl-3-substituted)-propenamido side-chain of fixed geometry. In vitro results for these compounds against a range of Gram-positive and Gram-nega
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3e4babc703f01918b656b1e7de7c6e4e
https://doi.org/10.7164/antibiotics.46.331
https://doi.org/10.7164/antibiotics.46.331
Publikováno v:
ChemInform. 22
Ring-fused 1,2-dithiolylium or isothiazolium salts were obtained by substitution of a sulphur atom for the grouping (R2NCS2Pd) in various cyclopalladated complexes [Pd(R2NCS2)L] derived from ligands (LH) containing Ar–CS or Ar–CN– substructures
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9a64028e440176c37fc69da3461958d3
https://doi.org/10.1002/chin.199107079
https://doi.org/10.1002/chin.199107079
Publikováno v:
ChemInform. 27
Acetylenic epoxy alcohol cyclizations provide an efficient stereocontrolled construction of functionalized, dihydroxylated cycloheptanoid ring systems.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ad20c26ad80990f75eb48016ea12bb1b
https://doi.org/10.1002/chin.199602108
https://doi.org/10.1002/chin.199602108
Publikováno v:
ChemInform. 30
The stereocontrolled construction of cycloheptanoid ring systems, relevant to sesquiterpenes and diterpenes of biological activity, is described. A new and highly efficient cyclization methodology ...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::21713bc265efe238901331fb80dd3699
https://doi.org/10.1002/chin.199912091
https://doi.org/10.1002/chin.199912091
Autor:
Jane McGregor, Trevor J. Grinter, Charles M. Marson, Timothy Charles Walsgrove, Harry Adams, Catriona A. Oare
Publikováno v:
ChemInform. 34
Treatment of an unsaturated 2,3-epoxy alcohol with SnBr 4 leads to a stereoselective formation of a cyclopropane ring, and an α-ketol unit as part of a subsequent ring expansion.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f80e26f0ca524e7fa9fa9e2f6b376f4e
https://doi.org/10.1002/chin.200313171
https://doi.org/10.1002/chin.200313171
Publikováno v:
Journal of the Chemical Society, Perkin Transactions 1. :2881
Ring-fused 1,2-dithiolylium or isothiazolium salts were obtained by substitution of a sulphur atom for the grouping (R2NCS2Pd) in various cyclopalladated complexes [Pd(R2NCS2)L] derived from ligands (LH) containing Ar–CS or Ar–CN– substructures
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a72f6a0f30cc16055d4d0e3a5d977e22
https://doi.org/10.1039/p19900002881
https://doi.org/10.1039/p19900002881
Publikováno v:
Tetrahedron Letters. 20:3339-3342
Isothiazolium and 1,2-dithiolylium salts containing fused rings have been synthesised from cyclometalated palladium complexes.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::89388af775891ca8fea66637e373aaa6
https://doi.org/10.1016/s0040-4039(01)95403-6
https://doi.org/10.1016/s0040-4039(01)95403-6
Publikováno v:
Inorganic and Nuclear Chemistry Letters. 16:145-147
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d2e3520b76ab5523f29322a44d21c981
https://doi.org/10.1016/0020-1650(80)80050-x
https://doi.org/10.1016/0020-1650(80)80050-x