| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A cyclic phosphonamidate analogue of glucose as a selective inhibitor of inverting glycosidases
|
Darrow, James W.
|
|
1996
|
4 |
8 |
p. 1341-1348
|
artikel
|
| 2 |
A highly practical synthesis of the sialyl Lewis X pentasaccharide and an investigation of binding to E-, P-, and L-Selectins
|
Kiyoi, Takao
|
|
1996
|
4 |
8 |
p. 1167-1176
|
artikel
|
| 3 |
3-Amino-2-hydroxy-propionaldehyde and 3-amino-1-hydroxypropan-2-one derivatives: New classes of aminopeptidase inhibitors
|
Tarnus, Céline
|
|
1996
|
4 |
8 |
p. 1287-1297
|
artikel
|
| 4 |
A new family of potential oncostatics: 2-chloroethylnitrososulfamides (CENS)—I. Synthesis, structure, and pharmacological evaluation (preliminary results)
|
Abdaoui, Mohamed
|
|
1996
|
4 |
8 |
p. 1227-1235
|
artikel
|
| 5 |
Announcements
|
|
|
1996
|
4 |
8 |
p. v
|
artikel
|
| 6 |
Applying Mosher's method to acetogenins bearing vicinal diols. The absolute configurations of muricatetrocin C and rollidecins A and B, new bioactive acetogenins from Rollinia mucosa
|
Shi, Guoen
|
|
1996
|
4 |
8 |
p. 1281-1286
|
artikel
|
| 7 |
A protein radical cage slows photolysis of methylcobalamin in methionine synthase from Escherichia coli
|
Jarrett, Joseph T.
|
|
1996
|
4 |
8 |
p. 1237-1246
|
artikel
|
| 8 |
Charge is the major discriminating factor for glutathione reductase versus trypanothione reductase inhibitors
|
Faerman, Carlos H.
|
|
1996
|
4 |
8 |
p. 1247-1253
|
artikel
|
| 9 |
cis-Gigantrionenin and 4-acetyl gigantetrocin A, two new bioactive annonaceous acetogenins from Goniothalamus giganteus, and the stereochemistries of acetogenin 1,2,5-triols
|
Zeng, Lu
|
|
1996
|
4 |
8 |
p. 1271-1279
|
artikel
|
| 10 |
Contributors to this issue
|
|
|
1996
|
4 |
8 |
p. vii-viii
|
artikel
|
| 11 |
Cytotoxic trichilin-type limonoids from Melia azedarach
|
Takeya, Koichi
|
|
1996
|
4 |
8 |
p. 1355-1359
|
artikel
|
| 12 |
Graphical abstracts
|
|
|
1996
|
4 |
8 |
p. ix-xv
|
artikel
|
| 13 |
Molecular structure and dynamics of some potent 5-HT3 receptor antagonists. Insight into the interaction with the receptor
|
Cappelli, Andrea
|
|
1996
|
4 |
8 |
p. 1255-1269
|
artikel
|
| 14 |
Properties of diacetyl (acetoin) reductase from Bacillus stearothermophilus
|
Paolo Giovannini, P.
|
|
1996
|
4 |
8 |
p. 1197-1201
|
artikel
|
| 15 |
Salen-anthraquinone Conjugates. Synthesis, DNA-binding and cleaving properties, effects on topoisomerases and cytotoxicity
|
Routier, Sylvain
|
|
1996
|
4 |
8 |
p. 1185-1196
|
artikel
|
| 16 |
SRS-A antagonist pyranoquinolone alkaloids from East African Fagara plants and their synthesis
|
Kamikawa, Tadao
|
|
1996
|
4 |
8 |
p. 1317-1320
|
artikel
|
| 17 |
Structure-activity relationships of HIV-1 PR inhibitors containing AHPBA—II. Modification of pyrrolidine ring at P1′ proline
|
Komai, Tomoaki
|
|
1996
|
4 |
8 |
p. 1365-1377
|
artikel
|
| 18 |
Synthesis and antitumor activity of duocarmycin derivatives: A-ring pyrrole analogues of duocarmycin B2
|
Nagamura, Satoru
|
|
1996
|
4 |
8 |
p. 1379-1391
|
artikel
|
| 19 |
Synthesis and biological evaluation of an electronically activated isooxacephem
|
Hakimelahi, Gholam H.
|
|
1996
|
4 |
8 |
p. 1361-1364
|
artikel
|
| 20 |
Synthesis and inhibitory properties of a thiomethylmercuric sialic acid with application to the X-ray structure determination of 9-O-acetylsialic acid esterase from influenza C virus
|
Fitz, Wolfgang
|
|
1996
|
4 |
8 |
p. 1349-1353
|
artikel
|
| 21 |
Synthesis and pharmacology of Alkanediguanidinium compounds that block the neuronal nicotinic acetylcholine receptor
|
Villarroya, Mercedes
|
|
1996
|
4 |
8 |
p. 1177-1183
|
artikel
|
| 22 |
Synthesis and properties of α- and β-oligodeoxynucleotides containing α- and β-1-(2-O-methyl-d-arabinofuranosyl)thymine
|
Gotfredsen, Charlotte H.
|
|
1996
|
4 |
8 |
p. 1217-1225
|
artikel
|
| 23 |
Synthesis of bis-γ-butyrolactones containing conformationally constrained (S)- and (R)-diacylglycerol structures
|
Lee, Jeewoo
|
|
1996
|
4 |
8 |
p. 1299-1305
|
artikel
|
| 24 |
Synthesis of 4,17-diazasteroid inhibitors of human 5α-reductase
|
Morzycki, Jacek W.
|
|
1996
|
4 |
8 |
p. 1209-1215
|
artikel
|
| 25 |
Tetrahedron prize for creativity in organic chemistry 1996
|
|
|
1996
|
4 |
8 |
p. iii
|
artikel
|
| 26 |
The high affinity melatonin binding site probed with conformationally restricted ligands—II. Homology modeling of the receptor
|
Grol, Cor J.
|
|
1996
|
4 |
8 |
p. 1333-1339
|
artikel
|
| 27 |
The high affinity melatonin binding site probed with conformationally restricted ligands—I. Pharmacophore and minireceptor models
|
Jansen, Johanna M.
|
|
1996
|
4 |
8 |
p. 1321-1332
|
artikel
|
| 28 |
The synthesis and in vitro antibacterial activity of conformationally restricted quinolone antibacterial agents
|
Cooper, Curt S.
|
|
1996
|
4 |
8 |
p. 1307-1315
|
artikel
|
| 29 |
Tyrphostins IV—Highly potent inhibitors of EGF receptor kinase. Structure-activity relationship study of 4-anilidoquinazolines
|
Gazit, Aviv
|
|
1996
|
4 |
8 |
p. 1203-1207
|
artikel
|
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