au.\*:("STACHULSKI, A. V")
Results 1 to 18 of 18
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Penicillin C-6 substitution: a novel oxygen-bridged dimerSTACHULSKI, A. V.Tetrahedron letters. 1985, Vol 26, Num 15, pp 1883-1884, issn 0040-4039Article
Penicillin C-6 substitution using the versatile 6α-succinimido-oxy leaving groupSTACHULSKI, A. V.Journal of the Chemical Society. Chemical communications. 1986, Num 5, pp 401-402, issn 0022-4936Article
Synthesis of O-vinyl oximes and derived penicillins using organoselenium intermediatesSTACHULSKI, A. V.Journal of the Chemical Society. Perkin transactions. I. 1991, Num 12, pp 3065-3070, issn 0300-922XArticle
Convenient synthesis of a novel γ-aminobutyric acid analogue: 4-amino-2,2-dimethylbutanoic acidSCHEINMANN, F; STACHULSKI, A. V.Journal of chemical research. Synopses (Print). 1993, Num 10, pp 414-415, issn 0308-2342Article
Biosynthesis. XXVI: Synthetic studies on structural modification of late biosynthetic precursors for colchicineBATTERSBY, A. R; MCDONALD, E; STACHULSKI, A. V et al.Journal of the Chemical Society. Perkin transactions. I. 1983, Vol 12, pp 3053-3063, issn 0300-922XArticle
Further synthetic studies in penicillin C(6)-substitution including the versatile 6α-succinimidooxy leaving groupMILNER, P. H; STACHULSKI, A. V.Journal of the Chemical Society. Perkin transactions. I. 1991, Num 10, pp 2343-2352, issn 0300-922XArticle
The synthesis of the glucuronide metabolite of UK-157,147 using immobilised uridine 5'-diphosphoglucuronyl transferase and traditional organic chemistry techniques (Imidate method)WEBSTER, R; BEAUMONT, K; RITZAU, M et al.Biocatalysis and biotransformation (Print). 2001, Vol 19, Num 1, pp 69-83, issn 1024-2422Article
The chemistry of some 2-aminothiazol-4-ylacetic acid derivatives and the synthesis of derived penicillinsHARDY, D. H; HARRINGTON, F. P; STACHULSKI, A. V et al.Journal of the Chemical Society. Perkin transactions. I. 1984, Num 6, pp 1227-1235, issn 0300-922XArticle
Aqueous and anhydrous degradations of 6α-formamidopenicillinsCUTMORE, E. A; GUEST, A. W; HATTO, J. D. I et al.Journal of the Chemical Society. Perkin transactions. I. 1990, Num 4, pp 847-853, issn 0300-922XArticle
Structure-activity relationships of some 6α-formamido penicillinsGUEST, A. W; HARRINGTON, F. P; MILNER, P. H et al.Journal of antibiotics (Tokyo. 1968). 1986, Vol 39, Num 10, pp 1498-1501, issn 0021-8820Article
Development of novel furanocoumarin dimers as potent and selective inhibitors of cyp3a4ROW, E; BROWN, S. A; STACHULSKI, A. V et al.Drug metabolism and disposition. 2006, Vol 34, Num 2, pp 324-330, issn 0090-9556, 7 p.Article
Synthesis of 8-geranyloxypsoralen analogues and their evaluation as inhibitors of CYP3A4ROW, E. C; BROWN, S. A; STACHULSKI, A. V et al.Bioorganic & medicinal chemistry. 2006, Vol 14, Num 11, pp 3865-3871, issn 0968-0896, 7 p.Article
Acetonitrile: an excellent solvent for the 1,1-dichloromethylenation of certain ketonesBURTON, G; ELDER, J. S; FELL, S. C. M et al.Tetrahedron letters. 1988, Vol 29, Num 2, pp 3003-3006, issn 0040-4039Article
6α(7α)-Formamido penicillins and cephalosporinsMILNER, P. H; GUEST, A. W; HARRINGTON, F. P et al.Journal of the Chemical Society. Chemical communications. 1984, Num 20, pp 1335-1336, issn 0022-4936Article
Synthesis and structure-activity relationships of some 6β-acrylamido penicillinsANDERSON, R. K; CHAPMAN, P. C; STACHULSKI, A. V et al.Journal of antibiotics (Tokyo. 1968). 1993, Vol 46, Num 2, pp 331-342, issn 0021-8820Article
Structure-activity relationships of some arylglycine analogues and catechol isosteres of brl 36650, a 6α-formamido penicillinBEST, D. J; BURTON, G; DAVIES, D. T et al.Journal of antibiotics (Tokyo. 1968). 1990, Vol 43, Num 5, pp 574-577, issn 0021-8820, 4 p.Article
Degradation of BRL 36650, a 6α-formamido penicillin: C(5)-C(6) bond cleavageCUTMORE, E. A; GUEST, A. W; HATTO, J. D. I et al.Journal of the Chemical Society. Chemical communications. 1987, Num 1, pp 21-23, issn 0022-4936Article