Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Robin A. Carr"'
Publikováno v:
Cancer Research. 83:2635-2635
Introduction: There is a need for ADC payloads with an improved therapeutic index, consequently we have coupled potent and selective inhibitors of NMT to trastuzumab to test their potential in both in vitro and in vivo models. Experimental Procedures
Autor:
M. Pass, J. R. Wheatcroft, Harry Finch, N. Bailey, P. Shah, J. E. Head, Robin E. Carr, B. Evans, J. W. B. Cooke, P. C. Box
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 7:281-286
The development of a potent, selective and orally bioavailable 1,5-benzodiazepindione gastrin/CCKB receptor antagonist (compound 7, GR199114X) is described.
Publikováno v:
Tetrahedron Letters. 37:5163-5166
Generation of azomethine ylides, imidate methylides, and thioimidate methylides which are exocyclic to indane, benzofuran, benzothiophene, and benzopyran moieties respectively, in the presence of electron deficient dipolarophiles, gives direct access
Publikováno v:
Tetrahedron Letters. 37:3915-3918
The γ-lactam based alkaloid cynometrine has been synthesised in four steps from 1-methyl-imidazole-4-carboxaldehyde. The key step involves an efficient regio-, stereo-, and chemoselective 1,3-dipolar cycloaddition of a dithiolane-fused azomethine yl
Publikováno v:
Tetrahedron Letters. 37:711-714
Dithiolane-isocyanate imminium methylides which are a new type of azomethine methylide-derived 1,3-dipole undergo efficient and regioselective cycloaddition to conjugated carbonyls and thiocarbonyls to yield predominantly 1,3-oxazolidine- and thiazol
Publikováno v:
Tetrahedron Letters. 36:9409-9412
Publikováno v:
ChemInform. 27
Publikováno v:
ChemInform. 27
Dithiolane-isocyanate imminium methylides which are a new type of azomethine methylide-derived 1,3-dipole undergo efficient and regioselective cycloaddition to conjugated carbonyls and thiocarbonyls to yield predominantly 1,3-oxazolidine- and thiazol
Publikováno v:
ChemInform. 27
The γ-lactam based alkaloid cynometrine has been synthesised in four steps from 1-methyl-imidazole-4-carboxaldehyde. The key step involves an efficient regio-, stereo-, and chemoselective 1,3-dipolar cycloaddition of a dithiolane-fused azomethine yl
Publikováno v:
ChemInform. 27
Generation of azomethine ylides, imidate methylides, and thioimidate methylides which are exocyclic to indane, benzofuran, benzothiophene, and benzopyran moieties respectively, in the presence of electron deficient dipolarophiles, gives direct access