Stefano Roelens
0000-0002-9763-3263
81 papers found
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Group 14 organometallic reagents. 11. Macrocyclic polylactones by catalyzed cyclooligomerization. Tetra[(S)-.beta.-butyrolactone]
Group 14 organometallic reagents. 12. An improved procedure for the synthesis of macrocyclic poly(thialactones). The dramatic effect of reactant mixing
Group 14 organometallic reagents. 9. Organotin-mediated monoacylation of diols with reversed chemoselectivity: a convenient synthetic method
2,2-Di-n-butyl-1,3,2-dioxastannolane/di-n-butyltin dichloride: an excellent catalytic system for cyclo-oligomerization of lactones
Organotin-mediated synthesis of macrocyclic tetraesters. A combined proton NMR spectroscopy, gel permeation chromatography, and fast atom bombardment mass spectrometry approach to complete product analysis
Group 14 organometallic reagents. 8. Organotin-mediated synthesis of macrocyclic tetraesters: regio- and stereochemistry
13C NMR studies of d- and l-phenylalanine binding to cobalt(II) carboxypeptidase A
Organotin-mediated synthesis of macrocyclic polyesters: mechanism and selectivity in the reaction of dioxastannolanes with diacyl dichlorides
Group 4 organometallic reagents. Part 6. The organotin-mediated monofunctionalization of diols: an insight into the selective monoesterification with acyl chlorides
Interaction of carbon dioxide and copper(II) carbonic anhydrase
Group 14 organometallic reagents. 4. Stereodynamics of substituted dioxastannolanes. Carbon-13 and tin-119 NMR studies
Co2 and Carbonic-Anhydrase
Group IVA organometallic reagents. 2. Enantiomeric purity determination of 1,2-diols through NMR spectroscopy without chiral auxiliaries
Group 4 organometallic reagents. A 1H, 13C and 119Sn nuclear magnetic resonance study on 2,2-dibutyl-1,3,2-dioxastannolane structure in solution
Regioselective acylation of glycols: evidence for organotin-mediated reversal of chemoselectivity
Activated C,H‐Acids: N‐Alkyl‐9‐fluorenimines. Preliminary communication
The Reaction of Pyruvic Acid with Amines and Aminoesters Reexamined. Preliminary communication
Substituent Effect Treatment of Interactions Between Contiguous Functionalities .4. Restraint to Phenyl-Nitrogen Conjugative Interaction in N-Functionalized N-Methylanilines
Substituent effect treatment of interactions between contiguous functionalities. IV. Hindrance to phenyl-nitrogen conjugative interaction in N-functionalized N-methylanilines
Ring-closure reactions. 10. A kinetic study for the formation of macrocyclic aromatic ethers. Lack of the rigid group effect on large ring formation
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