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M49
Received: 12 February 1998 / Published: 4 March 1998
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M50
Received: 16 February 1998 / Published: 4 March 1998
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M51
Received: 27 February 1998 / Published: 6 March 1998
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M52
Received: 27 February 1998 / Published: 6 March 1998
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M53
Received: 27 February 1998 / Published: 6 March 1998
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M54
Received: 27 February 1998 / Published: 6 March 1998
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M55
Received: 27 February 1998 / Published: 6 March 1998
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M56
Received: 27 February 1998 / Published: 6 March 1998
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M57
Received: 27 February 1998 / Published: 6 March 1998
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M58
Received: 27 February 1998 / Published: 6 March 1998
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M59
Received: 27 February 1998 / Published: 6 March 1998
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M60
Received: 27 February 1998 / Published: 6 March 1998
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M61
Received: 27 February 1998 / Published: 6 March 1998
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M62
Received: 27 February 1998 / Published: 6 March 1998
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M63
Received: 27 February 1998 / Published: 6 March 1998
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M64
Received: 27 February 1998 / Published: 6 March 1998
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M65
Received: 27 February 1998 / Published: 6 March 1998
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M66
Received: 27 February 1998 / Published: 6 March 1998
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M67
Received: 27 February 1998 / Published: 6 March 1998
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M68
Received: 27 February 1998 / Published: 6 March 1998
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M69
Received: 27 February 1998 / Published: 6 March 1998
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M70
Received: 27 February 1998 / Published: 6 March 1998
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M71
Received: 27 February 1998 / Published: 6 March 1998
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M72
Received: 27 February 1998 / Published: 6 March 1998
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M73
Received: 27 February 1998 / Published: 6 March 1998
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p. 51-59
Received: 11 January 1998 / Accepted: 13 February 1998 / Published: 17 February 1998
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| Download PDF Full-text (46 KB) Abstract: Homogeneous linear poly(tartrate ester) ligands provide high chemical yields and enantiomeric excesses in the epoxidation of trans -hex-2-en-1-ol using Ti(OPri )4 -tert -butyl hydroperoxide. Branched poly(tartrate ester) can be use as heterogeneous ligands in the epoxidation of trans -hex-2-en-1-ol using Ti(OPri )4 -tert -butyl hydroperoxide. Removal and recovery of the polymer catalyst is a simple filtration at the end of reactions.
p. 60-63
Received: 3 December 1997 / Accepted: 3 February 1998 / Published: 18 February 1998
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| Download PDF Full-text (22 KB) Abstract: Azomethine ylides were generated from Schiffs bases of S -allylcysteine methyl ester and their intramolecular 1,3-dipolar cycloadditions were studied. These reactions led to the synthesis of thieno[3,4-b ]pyrrole derivatives in good yield.
p. 64-70
Received: 10 January 1998 / Accepted: 16 February 1998 / Published: 20 February 1998
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| Download PDF Full-text (52 KB) Abstract: A synthetic route developed for the preparation of the A-ring of Taxol family of molecules is reported. By means of an intramolecular Diels-Alder reaction an asymmetric approach to this ring has been accomplished. Also, initial studies to prepare the A ring using an intramolecular Diels-Alder reaction have been successful.
p. 71-79
Received: 30 October 1997 / Accepted: 18 January 1998 / Published: 23 February 1998
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| Download PDF Full-text (50 KB) Abstract: 3-Substituted 1,2,4-triazole derivatives (5, 9, 13, 16b, 19), pyrimidinium salts (21), triazines (24), and aryl methylene hydrazono pyrazolopyrano-pyrimidine (27a,b) which are rearranged in basic medium to 30a,b, were afforded via the reaction of 6-amino 1,4,5,6-tetrahydro-5-imino-3-methyl-1-phenyl-4 (pchlorophenyl) pyrazolo [4', 3' : 5,6]-pyrano [2,3-d] pyrimidine (3) with different reagents.
p. 80-87
Received: 15 January 1998 / Accepted: 23 February 1998 / Published: 24 February 1998
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| Download PDF Full-text (43 KB) Abstract: The title compound was synthesized from sorbic acid by an eight step sequence. The key step was the stereospecific intramolecular Diels-Alder reaction of the acylnitroso derivative of N-sorbyl-L-proline (5). L-Proline served as a temporary tether which directed both the stereochemistry and the regiochemistry of the cycloaddition.
p. 88-93
Received: 19 February 1998 / Accepted: 3 March 1998 / Published: 5 March 1998
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| Download PDF Full-text (55 KB) Abstract: 3(2)-Naphthofuranone (1) was condensed in the presence of Al2 O3 -KF with aromatic aldehydes (4) to give arylidenenaphthofuranones (5a-f) without solvent under focused microwave irradiation.
p. 94-99
Received: 3 March 1998 / Accepted: 6 March 1998 / Published: 9 March 1998
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| Download PDF Full-text (414 KB) Abstract: The background to a Web page describing elemental and molecular heritage at Imperial College chemistry department is described. Photographs are shown of the original samples of elemental bromine and crystalline silicon, and molecular ferrocene and mauveine. 3D "Hyperactive" models of these systems are shown, together with a recently discovered heterocyclic systems scorpionine, which like mauveine is made by a deceptively simple chemical synthesis.
p. 100-106
Received: 28 January 1998 / Accepted: 18 February 1998 / Published: 9 March 1998
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| Download PDF Full-text (41 KB) Abstract: An efficient one-pot synthesis of 5-acyl-1,2,3,4-tetrahydropyrimidine-2-thiones/ones is described. The synthesis is based on the reaction of readily available α-tosyl substituted thioureas or ureas with enolates of β-oxoesters or 1,3-dicarbonyl compounds followed by acid-catalyzed dehydration of the obtained 5-acyl-4-hydroxyhexahydropyrimidine-2-thiones/ones.
p. 107-119
Received: 2 November 1997 / Accepted: 23 February 1998 / Published: 10 March 1998
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| Download PDF Full-text (466 KB) Abstract: Both enantiomers of rolipram (1) have been prepared in large quantity from a common intermediate rac -3-(3’-cyclopentyloxy-4’-methoxy)phenyl-4-nitro butyric acid (6), which was resolved by way of the two readily separable diastereoisomeric amides obtained with (S)-(-)-phenylethylamine. Reduction of the nitro group and intramolecular transamidation gave (R)-(-)-1 and (S)-(+)-1, respectively. CD spectra of both enantiomers of rolipram are reported and discussed. Both enantiomers of rolipram presented the same potency of inhibitory activity against recombinant cyclic-AMP-selective phosphodiesterase (PDE4) subtypes.
p. 120-131
Received: 16 January 1998 / Accepted: 17 February 1998 / Published: 10 March 1998
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| Download PDF Full-text (68 KB) Abstract: The 3-Acyl-2-R-methylchromones (R = H, ArO, C6 H4 (CO)2 N) were prepared in good yields by different methods from 2-hydroxyaroylacetone derivatives. Some subsequent reactions of these compounds with hydroxylamine and 3-formylchromones are described. The effect of microwave irradation on some condensation reactions was studied.
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