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Results: 1-15 |
Results: 15
Carbocyclic serine analogues: regio- and diastereoselective syntheses of new 1-amino-2,5-dihydroxycyclohexanecarboxylic acids
Authors: Clerici, F Gelmi, ML Gambini, A Nava, D
Citation: F. Clerici et al., Carbocyclic serine analogues: regio- and diastereoselective syntheses of new 1-amino-2,5-dihydroxycyclohexanecarboxylic acids, TETRAHEDRON, 57(30), 2001, pp. 6429-6438
Isothiazoles. Part 12: Isothiazolylphosphonates, a new class of isothiazole dioxides
Authors: Clerici, F Gelmi, ML Pini, E Valle, M
Citation: F. Clerici et al., Isothiazoles. Part 12: Isothiazolylphosphonates, a new class of isothiazole dioxides, TETRAHEDRON, 57(25), 2001, pp. 5455-5459
Asymmetric synthesis of 2-amino-3-hydroxynorbornene-2-carboxylic acid derivatives
Authors: Abbiati, G Clerici, F Gelmi, ML Gambini, A Pilati, T
Citation: G. Abbiati et al., Asymmetric synthesis of 2-amino-3-hydroxynorbornene-2-carboxylic acid derivatives, J ORG CHEM, 66(19), 2001, pp. 6299-6304
A highly diastereoselective synthesis of new polyhydroxy 2-aminonorbornanecarboxylic acids
Authors: Clerici, F Gelmi, ML Gambini, A
Citation: F. Clerici et al., A highly diastereoselective synthesis of new polyhydroxy 2-aminonorbornanecarboxylic acids, J ORG CHEM, 66(14), 2001, pp. 4941-4944
2-Amidinylindole-3-carbaldehydes: Versatile synthons for the preparation of alpha-carboline derivatives
Authors: Erba, E Gelmi, ML Pocar, D
Citation: E. Erba et al., 2-Amidinylindole-3-carbaldehydes: Versatile synthons for the preparation of alpha-carboline derivatives, TETRAHEDRON, 56(51), 2000, pp. 9991-9997
Isothiazoles. Part 11: 3-azahexatrienes from 2-arylpropenamidines: Electrocyclization to 6-aminonicotinic acid derivatives
Authors: Beccalli, EM Clerici, F Gelmi, ML
Citation: Em. Beccalli et al., Isothiazoles. Part 11: 3-azahexatrienes from 2-arylpropenamidines: Electrocyclization to 6-aminonicotinic acid derivatives, TETRAHEDRON, 56(27), 2000, pp. 4817-4821
Conformationally constrained serine analogues: Synthesis of new 2-amino-3-hydroxynorbornanecarboxylic acid derivatives
Authors: Clerici, F Gelmi, ML Gambini, A
Citation: F. Clerici et al., Conformationally constrained serine analogues: Synthesis of new 2-amino-3-hydroxynorbornanecarboxylic acid derivatives, J ORG CHEM, 65(19), 2000, pp. 6138-6141
A new access to diarylmaleic anhydrides
Authors: Beccalli, EM Gelmi, ML Marchesini, A
Citation: Em. Beccalli et al., A new access to diarylmaleic anhydrides, EUR J ORG C, (6), 1999, pp. 1421-1426
Isothiazoles. Part IX. An efficient synthetic route to 5-substituted-3-amino-4-arylisothiazole 1,1-dioxides and their 4,5-dihydro derivatives.
Authors: Beccalli, EM Clerici, F Gelmi, ML
Citation: Em. Beccalli et al., Isothiazoles. Part IX. An efficient synthetic route to 5-substituted-3-amino-4-arylisothiazole 1,1-dioxides and their 4,5-dihydro derivatives., TETRAHEDRON, 55(7), 1999, pp. 2001-2012
Isothiazoles. Part X. New 3-substituted-2-arylpropenamidines by base catalyzed ring opening of 3-amino-4-arylisothiazole 1,1-dioxides.
Authors: Beccalli, EM Clerici, F Gelmi, ML
Citation: Em. Beccalli et al., Isothiazoles. Part X. New 3-substituted-2-arylpropenamidines by base catalyzed ring opening of 3-amino-4-arylisothiazole 1,1-dioxides., TETRAHEDRON, 55(52), 1999, pp. 14975-14984
5(4H)-oxazolones. Part XIII. A new synthesis of 4-ylidene-5(4H)-oxazolonesby the Stille reaction.
Authors: Beccalli, EM Clerici, F Gelmi, ML
Citation: Em. Beccalli et al., 5(4H)-oxazolones. Part XIII. A new synthesis of 4-ylidene-5(4H)-oxazolonesby the Stille reaction., TETRAHEDRON, 55(3), 1999, pp. 781-786
6-chloro-spirocyclohexenindol-2-ones: an unusual ring transformation to ethyl 2-(cyclohexa-1,4-dienyl)phenylcarbamates.
Authors: Beccalli, EM Clerici, F Gelmi, ML
Citation: Em. Beccalli et al., 6-chloro-spirocyclohexenindol-2-ones: an unusual ring transformation to ethyl 2-(cyclohexa-1,4-dienyl)phenylcarbamates., TETRAHEDRON, 55(28), 1999, pp. 8579-8586
A novel class of conformationally constrained, masked cysteines: Synthesisof 2-alkyl- and 2-arylsulfanyl-1-aminocyclopropanecarboxylic acids
Authors: Clerici, F Gelmi, ML Pocar, D
Citation: F. Clerici et al., A novel class of conformationally constrained, masked cysteines: Synthesisof 2-alkyl- and 2-arylsulfanyl-1-aminocyclopropanecarboxylic acids, J ORG CHEM, 64(3), 1999, pp. 726-730
A highly diastereoselective approach to conformationally constrained serine analogues: Synthesis of an alpha-amino-beta-hydroxycyclohexenecarboxylic acid and derivatives
Authors: Clerici, F Gelmi, ML Gambini, A
Citation: F. Clerici et al., A highly diastereoselective approach to conformationally constrained serine analogues: Synthesis of an alpha-amino-beta-hydroxycyclohexenecarboxylic acid and derivatives, J ORG CHEM, 64(16), 1999, pp. 5764-5767
N-deacetyl-N-aminoacylthiocolchicine derivatives: Synthesis and biologicalevaluation on MDR-positive and MDR-negative human cancer cell lines
Authors: Gelmi, ML Mottadelli, S Pocar, D Riva, A Bombardelli, E De Vincenzo, R Scambia, G
Citation: Ml. Gelmi et al., N-deacetyl-N-aminoacylthiocolchicine derivatives: Synthesis and biologicalevaluation on MDR-positive and MDR-negative human cancer cell lines, J MED CHEM, 42(25), 1999, pp. 5272-5276
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