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Results: 1-13 |
Results: 13
Variable strategy toward carbasugars and relatives. 2. Diversity-based synthesis of beta-D-xylo, beta-D-ribo, beta-L-arabino, and beta-L-lyxo 4a-carbafuranoses and (4a-carbafuranosyl)thiols
Authors: Rassu, G Auzzas, L Pinna, L Zambrano, V Battistini, L Zanardi, F Marzocchi, L Acquotti, D Casiraghi, G
Citation: G. Rassu et al., Variable strategy toward carbasugars and relatives. 2. Diversity-based synthesis of beta-D-xylo, beta-D-ribo, beta-L-arabino, and beta-L-lyxo 4a-carbafuranoses and (4a-carbafuranosyl)thiols, J ORG CHEM, 66(24), 2001, pp. 8070-8075
The synthetic utility of furan-, pyrrole- and thiophene-based 2-silyloxy dienes
Authors: Rassu, G Zanardi, F Battistini, L Casiraghi, G
Citation: G. Rassu et al., The synthetic utility of furan-, pyrrole- and thiophene-based 2-silyloxy dienes, CHEM SOC RE, 29(2), 2000, pp. 109-118
Synthesis and utility of novel C-meso-glycosylated metalloporphyrins
Authors: Cornia, M Menozzi, M Ragg, E Mazzini, S Scarafoni, A Zanardi, F Casiraghi, G
Citation: M. Cornia et al., Synthesis and utility of novel C-meso-glycosylated metalloporphyrins, TETRAHEDRON, 56(24), 2000, pp. 3977-3983
Vinylogous aldol reaction of heterocyclic silyloxy dienes. Application in synthesis
Authors: Casiraghi, G Zanardi, F Rassu, G
Citation: G. Casiraghi et al., Vinylogous aldol reaction of heterocyclic silyloxy dienes. Application in synthesis, PUR A CHEM, 72(9), 2000, pp. 1645-1648
The utility of furan-, pyrrole-, and thiophene-based 2-silyloxy dienes as demonstrated by modular synthesis of annonaceous acetogenin core units and their pyrrolidine and thiolane analogues
Authors: Zanardi, F Battistini, L Rassu, G Auzzas, L Pinna, L Marzocchi, L Acquotti, D Casiraghi, G
Citation: F. Zanardi et al., The utility of furan-, pyrrole-, and thiophene-based 2-silyloxy dienes as demonstrated by modular synthesis of annonaceous acetogenin core units and their pyrrolidine and thiolane analogues, J ORG CHEM, 65(7), 2000, pp. 2048-2064
Variable strategy toward carbasugars and relatives. 1. Stereocontrolled synthesis of pseudo-beta-D-gulopyranose, pseudo-beta-D-xylofuranose, (pseudo-beta-D-gulopyranosyl)amine, and (pseudo-beta-D-xylofuranosyl)amine
Authors: Rassu, G Auzzas, L Pinna, L Battistini, L Zanardi, F Marzocchi, L Acquotti, D Casiraghi, G
Citation: G. Rassu et al., Variable strategy toward carbasugars and relatives. 1. Stereocontrolled synthesis of pseudo-beta-D-gulopyranose, pseudo-beta-D-xylofuranose, (pseudo-beta-D-gulopyranosyl)amine, and (pseudo-beta-D-xylofuranosyl)amine, J ORG CHEM, 65(20), 2000, pp. 6307-6318
The vinylogous aldol reaction: A valuable, yet understated carbon-carbon bond-forming maneuver
Authors: Casiraghi, G Zanardi, F Appendino, G Rassu, G
Citation: G. Casiraghi et al., The vinylogous aldol reaction: A valuable, yet understated carbon-carbon bond-forming maneuver, CHEM REV, 100(6), 2000, pp. 1929-1972
Variable strategy toward carbasugars and relatives as illustrated by diastereoselective synthesis of 1-deoxy-1-amino-pseudo-beta-D-gulopyranose (alias 1,2,4-tri-epi-validamine)
Authors: Rassu, G Auzzas, L Pinna, L Zanardi, F Battistini, L Casiraghi, G
Citation: G. Rassu et al., Variable strategy toward carbasugars and relatives as illustrated by diastereoselective synthesis of 1-deoxy-1-amino-pseudo-beta-D-gulopyranose (alias 1,2,4-tri-epi-validamine), ORG LETT, 1(8), 1999, pp. 1213-1215
Lewis acid assisted vinylogous Mannich and Mukaiyama aldol reactions: A route to densely hydroxylated indolizidine alkaloid analogues
Authors: Rassu, G Carta, P Pinna, L Battistini, L Zanardi, F Acquotti, D Casiraghi, G
Citation: G. Rassu et al., Lewis acid assisted vinylogous Mannich and Mukaiyama aldol reactions: A route to densely hydroxylated indolizidine alkaloid analogues, EUR J ORG C, (6), 1999, pp. 1395-1400
Diastereoselective synthesis of a novel lactam peptidomimetic exploiting vinylogous Mannich addition of 2-silyloxyfuran reagents
Authors: Battistini, L Rassu, G Pinna, L Zanardi, F Casiraghi, G
Citation: L. Battistini et al., Diastereoselective synthesis of a novel lactam peptidomimetic exploiting vinylogous Mannich addition of 2-silyloxyfuran reagents, TETRAHEDR-A, 10(4), 1999, pp. 765-773
The vinylogous aldol addition of heterocyclic silyloxy dienes: Applicationin synthesis
Authors: Rassu, G Zanardi, F Battistini, L Casiraghi, G
Citation: G. Rassu et al., The vinylogous aldol addition of heterocyclic silyloxy dienes: Applicationin synthesis, SYNLETT, (9), 1999, pp. 1333-1350
Asymmetric access to functional, structurally diverse molecules exploitingfive-membered heterocyclic silyloxy dienes
Authors: Casiraghi, G Rassu, G Zanardi, F Battistini, L
Citation: G. Casiraghi et al., Asymmetric access to functional, structurally diverse molecules exploitingfive-membered heterocyclic silyloxy dienes, ADV ASYMM S, 3, 1998, pp. 113-189
Furan-, pyrrole-, and thiophene-based siloxydienes en route to carbohydrate mimics and alkaloids
Authors: Casiraghi, G Rassu, G Zanardi, F
Citation: G. Casiraghi et al., Furan-, pyrrole-, and thiophene-based siloxydienes en route to carbohydrate mimics and alkaloids, CARBOHYDRATE MIMICS, 1998, pp. 327-347
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