RINALDI, Samuele

RINALDI, Samuele  

Dipartimento Scienze della Vita e dell'Ambiente  

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Risultati 1 - 20 di 56 (tempo di esecuzione: 0.023 secondi).
Titolo Data di pubblicazione Autore(i) File
A Bifunctional β-Isocupreidine Derivative as Catalyst for the EnantioselectiveMorita–Baylis–Hillman Reaction and a Mechanistic Rationale forEnantioselectivity 1-gen-2012 Martelli, Gianluca; Orena, Mario; Rinaldi, Samuele
A Highly Diastereoselective TiCl4-Mediated Reduction of β-Hydroxy Ketones with BH3·py A Very Efficient and General Synthesis of syn-1,3-Diols 1-gen-2001 G., Bartoli; M., Bosco; E., Marcantoni; M., Massaccesi; Rinaldi, Samuele; L., Sambri
A novel conformationally restricted analogue of 3-methylaspartic acid via stereoselective methylation of chiral pyrrolidin-2-ones 1-gen-2010 Crucianelli, E.; Galeazzi, Roberta; Martelli, G.; Orena, Mario; Rinaldi, Samuele; Sabatino, P.
A simple asymmetric synthesis of (+)- and (-)-2,6-diaminopimelics acids 1-gen-2000 F., Paradisi; G., Porzi; Rinaldi, Samuele; S., Sandri
a-methylene-b-trichloroacetylamino alkanoates from trichloroacetimidates of the Baylis-Hillman adducts 1-gen-2004 Galeazzi, Roberta; Martelli, G.; Orena, M.; Rinaldi, Samuele
Acid hydrolysis of an ether bond assisted by the neighbouring amide group: effects induced by salts and by structural changes part 6. 1-gen-2002 A., Arcelli; F., Paradisi; G., Porzi; Rinaldi, Samuele; S., Sandri
Acidity effect on the cleavage of ether function intramolecularly assisted by the amide group. Part 5. 1-gen-2001 A., Arcelli; R., Cecchi; G., Porzi; Rinaldi, Samuele; S., Sandri
Ammonolysis of morpholine-2,5-diones: participation of the primary amide group. Part 2 1-gen-2012 Arcelli, A.; Bongini, A.; Porzi, G.; Rinaldi, Samuele
An efficient acid hydrolysis of the ether bond assisted by the neighbouring benzamide group Part 3. 1-gen-2001 A., Arcelli; G., Porzi; Rinaldi, Samuele; S., Sandri
Analogues of both Leu- and Met-enkephalin containing a constrained dipeptide isostere prepared from a Baylis-Hillman adduct 1-gen-2010 Galeazzi, Roberta; Martelli, G.; Marcucci, E.; Orena, Mario; Rinaldi, Samuele; Lattanzi, R.; Negri, L.
Analogues of nucleosides: synthesis of chiral pyrrolidin-2-ones or pyrrolidines-bearing nucleobases 1-gen-2014 Martelli, Gianluca; Monsignori, Antonella; Orena, Mario; Rinaldi, Samuele
beta-Peptoids: synthesis of a novel dimer having a fully extendedconformation 1-gen-2012 Martelli, Gianluca; Monsignori, Antonella; Orena, Mario; Rinaldi, Samuele; Castellucci, N.; Tomasini, C. .
Chiral 3-hydroxypyrrolidin-2-ones from a Baylis–Hillman adduct: convergent, stereoselective synthesis of a glycosidase inhibitor 1-gen-2004 Galeazzi, Roberta; G., Martelli; Mobbili, Giovanna; Orena, Mario; Rinaldi, Samuele
Chiral 3-hydroxypyrrolidin-2-ones. Part 2. Stereodivergent synthesis of conformationally restricted analogues of beta-homoserine 1-gen-2005 Galeazzi, Roberta; Martelli, G.; Natali, D.; Orena, Mario; Rinaldi, Samuele
Computational DFT Investigation of Vicinal Amide Group Anchimeric Assistance in Ether Cleavage 1-gen-2008 Calvaresi, M.; Rinaldi, Samuele; Arcelli, A.; Garavelli, M.
Conformational Studies by Dynamic NMR. 88.1 Stereomutation Processes in Diastereoisomers of a Representative Amino Alcohol and Related Amide Precursors 1-gen-2002 G., Bartoli; S., Grilli; L., Lunazzi; M., Massaccesi; A., Mazzanti; Rinaldi, Samuele
Conformationally Restricted Analogues of both (S)-beta-Homoserine and (S)-Aspartic Acid from Chiral 3-Acylamino Pyrrolidin-2-ones 1-gen-2005 Galeazzi, Roberta; Martelli, G.; Orena, Mario; Rinaldi, Samuele; Sabatino, P.
Diastereoselective functionalization of Baylis-Hillman adducts: A convenient approach to α-methyl-α-amino acids 1-gen-2010 Martelli, G.; Orena, Mario; Rinaldi, Samuele; Sabatino, P.
The diverse world of foldamers: Endless possibilities of self-assembly 1-gen-2020 Rinaldi, S.
Effect of neighbouring amide group bulkiness on anchimerically assisted ether bond cleavage: Part 7. 1-gen-2004 A., Arcelli; G., Porzi; Rinaldi, Samuele; S., Sandri