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Enabling cooperative educational game design on the web

after-school settings

Ahmadi N, Jazayeri M, Landoni M.
GSID: A1j_g25vPo0J
N Ahmadi, M Jazayeri, M Landoni - International Conference on …, 2012 - Springer

Educational game design environments enable end users to create computer games and are used as an engaging medium to teach programming to novice programmers. Although …

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Ahmadi, N., Jazayeri, M., & Landoni, M. (2012, September). Enabling cooperative educational game design on the web. In International Conference on Cooperative Design, Visualization and Engineering (pp. 57-64). Springer, Berlin, Heidelberg.
Ahmadi, Navid, Mehdi Jazayeri, and Monica Landoni. "Enabling cooperative educational game design on the web." International Conference on Cooperative Design, Visualization and Engineering. Springer, Berlin, Heidelberg, 2012.
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Gold(I)-catalyzed synthesis of γ-vinylbutyrolactones by intramolecular oxaallylic alkylation with alcohols.

Beilstein journal of organic chemistry

Chiarucci M, Locritani M, Cera G, Bandini M.
PMID: 21977203
Beilstein J Org Chem. 2011;7:1198-204. doi: 10.3762/bjoc.7.139. Epub 2011 Sep 01.

Gold(I)-N-heterocyclic carbene (NHC) complexes proved to be a reliable catalytic system for the direct synthesis of functionalized γ-vinylbutyrolactones by intramolecular oxaallylic alkylation with primary alcohols. Good isolated chemical yields were obtained for a range of malonyl and acetate derivatives....

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Chiarucci M, Locritani M, Cera G, et al. Gold(I)-catalyzed synthesis of γ-vinylbutyrolactones by intramolecular oxaallylic alkylation with alcohols. Beilstein J Org Chem. 2011;7:1198-204doi: 10.3762/bjoc.7.139.
Chiarucci, M., Locritani, M., Cera, G., & Bandini, M. (2011). Gold(I)-catalyzed synthesis of γ-vinylbutyrolactones by intramolecular oxaallylic alkylation with alcohols. Beilstein journal of organic chemistry, 71198-204. https://doi.org/10.3762/bjoc.7.139
Chiarucci, Michel, et al. "Gold(I)-catalyzed synthesis of γ-vinylbutyrolactones by intramolecular oxaallylic alkylation with alcohols." Beilstein journal of organic chemistry vol. 7 (2011): 1198-204. doi: https://doi.org/10.3762/bjoc.7.139
Chiarucci M, Locritani M, Cera G, Bandini M. Gold(I)-catalyzed synthesis of γ-vinylbutyrolactones by intramolecular oxaallylic alkylation with alcohols. Beilstein J Org Chem. 2011;7:1198-204. doi: 10.3762/bjoc.7.139. Epub 2011 Sep 01. PMID: 21977203; PMCID: PMC3182428.
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Metastability and avalanche dynamics in strongly correlated gases with long-range interactions.

Proceedings of the National Academy of Sciences of the United States of America

Hruby L, Dogra N, Landini M, Donner T, Esslinger T.
PMID: 29519875
Proc Natl Acad Sci U S A. 2018 Mar 27;115(13):3279-3284. doi: 10.1073/pnas.1720415115. Epub 2018 Mar 08.

We experimentally study the stability of a bosonic Mott insulator against the formation of a density wave induced by long-range interactions and characterize the intrinsic dynamics between these two states. The Mott insulator is created in a quantum degenerate...

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Hruby L, Dogra N, Landini M, et al. Metastability and avalanche dynamics in strongly correlated gases with long-range interactions. Proc Natl Acad Sci U S A. 2018;115(13):3279-3284doi: 10.1073/pnas.1720415115.
Hruby, L., Dogra, N., Landini, M., Donner, T., & Esslinger, T. (2018). Metastability and avalanche dynamics in strongly correlated gases with long-range interactions. Proceedings of the National Academy of Sciences of the United States of America, 115(13), 3279-3284. https://doi.org/10.1073/pnas.1720415115
Hruby, Lorenz, et al. "Metastability and avalanche dynamics in strongly correlated gases with long-range interactions." Proceedings of the National Academy of Sciences of the United States of America vol. 115,13 (2018): 3279-3284. doi: https://doi.org/10.1073/pnas.1720415115
Hruby L, Dogra N, Landini M, Donner T, Esslinger T. Metastability and avalanche dynamics in strongly correlated gases with long-range interactions. Proc Natl Acad Sci U S A. 2018 Mar 27;115(13):3279-3284. doi: 10.1073/pnas.1720415115. Epub 2018 Mar 08. PMID: 29519875; PMCID: PMC5879698.
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Visible-Light-Induced Direct Photocatalytic Carboxylation of Indoles with CBr4 /MeOH.

Chemistry (Weinheim an der Bergstrasse, Germany)

Yang QQ, Marchini M, Xiao WJ, Ceroni P, Bandini M.
PMID: 26509744
Chemistry. 2015 Dec 07;21(50):18052-6. doi: 10.1002/chem.201503787. Epub 2015 Oct 28.

Photocatalysis enables the cascade reactions of indoles and CBr4 in MeOH through a C(sp(2) )H functionalization/methanolysis sequence. The title reaction provides an efficient access to indole 2- and 3-carboxylates in a single operation (no preinstallation of protecting as well...

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Yang QQ, Marchini M, Xiao WJ, et al. Visible-Light-Induced Direct Photocatalytic Carboxylation of Indoles with CBr4 /MeOH. Chemistry. 2015;21(50):18052-6doi: 10.1002/chem.201503787.
Yang, Q. Q., Marchini, M., Xiao, W. J., Ceroni, P., & Bandini, M. (2015). Visible-Light-Induced Direct Photocatalytic Carboxylation of Indoles with CBr4 /MeOH. Chemistry (Weinheim an der Bergstrasse, Germany), 21(50), 18052-6. https://doi.org/10.1002/chem.201503787
Yang, Qing-Qing, et al. "Visible-Light-Induced Direct Photocatalytic Carboxylation of Indoles with CBr4 /MeOH." Chemistry (Weinheim an der Bergstrasse, Germany) vol. 21,50 (2015): 18052-6. doi: https://doi.org/10.1002/chem.201503787
Yang QQ, Marchini M, Xiao WJ, Ceroni P, Bandini M. Visible-Light-Induced Direct Photocatalytic Carboxylation of Indoles with CBr4 /MeOH. Chemistry. 2015 Dec 07;21(50):18052-6. doi: 10.1002/chem.201503787. Epub 2015 Oct 28. PMID: 26509744.
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Obesity Prevention for Children with Developmental Disabilities.

Current obesity reports

Must A, Curtin C, Hubbard K, Sikich L, Bedford J, Bandini L.
PMID: 25530916
Curr Obes Rep. 2014 Jun;3(2):156-70. doi: 10.1007/s13679-014-0098-7.

The prevention of obesity in children with DD is a pressing public health issue, with implications for health status, independent living, and quality of life. Substantial evidence suggests that children with developmental disabilities (DD), including those with intellectual disabilities...

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Must A, Curtin C, Hubbard K, et al. Obesity Prevention for Children with Developmental Disabilities. Curr Obes Rep. 2014;3(2):156-70doi: 10.1007/s13679-014-0098-7.
Must, A., Curtin, C., Hubbard, K., Sikich, L., Bedford, J., & Bandini, L. (2014). Obesity Prevention for Children with Developmental Disabilities. Current obesity reports, 3(2), 156-70. https://doi.org/10.1007/s13679-014-0098-7
Must, Aviva, et al. "Obesity Prevention for Children with Developmental Disabilities." Current obesity reports vol. 3,2 (2014): 156-70. doi: https://doi.org/10.1007/s13679-014-0098-7
Must A, Curtin C, Hubbard K, Sikich L, Bedford J, Bandini L. Obesity Prevention for Children with Developmental Disabilities. Curr Obes Rep. 2014 Jun;3(2):156-70. doi: 10.1007/s13679-014-0098-7. PMID: 25530916; PMCID: PMC4267572.
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[Cr(Salen)] as a 'bridge' between asymmetric catalysis, Lewis acids and redox processes.

Chemical communications (Cambridge, England)

Bandini M, Cozzi PG, Umani-Ronchi A.
PMID: 12123051
Chem Commun (Camb). 2002 May 07;(9):919-27. doi: 10.1039/b109945k.

An overview focused on the synthesis, structural features and catalytic applications of chiral [Cr(Salen)] complexes is presented. Key aspects of modern organic chemistry such as Lewis acids, asymmetric catalysis and redox processes are strictly connected with chronium-Schiff base complexes....

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Bandini M, Cozzi PG, Umani-Ronchi A. [Cr(Salen)] as a 'bridge' between asymmetric catalysis, Lewis acids and redox processes. Chem Commun (Camb). 2002;(9):919-27doi: 10.1039/b109945k.
Bandini, M., Cozzi, P. G., & Umani-Ronchi, A. (2002). [Cr(Salen)] as a 'bridge' between asymmetric catalysis, Lewis acids and redox processes. Chemical communications (Cambridge, England), (9), 919-27. https://doi.org/10.1039/b109945k
Bandini, Marco, et al. "[Cr(Salen)] as a 'bridge' between asymmetric catalysis, Lewis acids and redox processes." Chemical communications (Cambridge, England) vol. ,9 (2002): 919-27. doi: https://doi.org/10.1039/b109945k
Bandini M, Cozzi PG, Umani-Ronchi A. [Cr(Salen)] as a 'bridge' between asymmetric catalysis, Lewis acids and redox processes. Chem Commun (Camb). 2002 May 07;(9):919-27. doi: 10.1039/b109945k. PMID: 12123051.
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Sequential one-pot InBr(3)-catalyzed 1,4- then 1,2-nucleophilic addition to enones.

The Journal of organic chemistry

Bandini M, Cozzi PG, Giacomini M, Melchiorre P, Selva S, Umani-Ronchi A.
PMID: 12027683
J Org Chem. 2002 May 31;67(11):3700-4. doi: 10.1021/jo0163243.

Low sensitivity toward traces of moisture and high tolerance of different functional groups make indium tribromide suitable for carrying out multistep synthetic sequences. In particular, we have realized a 1,4-conjugated addition of indoles/thiols to alpha,beta-unsaturated ketones mediated by a...

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Bandini M, Cozzi PG, Giacomini M, et al. Sequential one-pot InBr(3)-catalyzed 1,4- then 1,2-nucleophilic addition to enones. J Org Chem. 2002;67(11):3700-4doi: 10.1021/jo0163243.
Bandini, M., Cozzi, P. G., Giacomini, M., Melchiorre, P., Selva, S., & Umani-Ronchi, A. (2002). Sequential one-pot InBr(3)-catalyzed 1,4- then 1,2-nucleophilic addition to enones. The Journal of organic chemistry, 67(11), 3700-4. https://doi.org/10.1021/jo0163243
Bandini, Marco, et al. "Sequential one-pot InBr(3)-catalyzed 1,4- then 1,2-nucleophilic addition to enones." The Journal of organic chemistry vol. 67,11 (2002): 3700-4. doi: https://doi.org/10.1021/jo0163243
Bandini M, Cozzi PG, Giacomini M, Melchiorre P, Selva S, Umani-Ronchi A. Sequential one-pot InBr(3)-catalyzed 1,4- then 1,2-nucleophilic addition to enones. J Org Chem. 2002 May 31;67(11):3700-4. doi: 10.1021/jo0163243. PMID: 12027683.
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Quantitative Texture Analysis in Two-Dimensional Echocardiography: Application to the Diagnosis of Myocardial Hemochromatosis.

Echocardiography (Mount Kisco, N.Y.)

Lattanzi F, Bellotti P, Picano E, Chiarella F, Paterni M, Forni G, Landini L, Distante A, Vecchio C.
PMID: 11442899
Echocardiography. 1996 Jan;13(1):9-20. doi: 10.1111/j.1540-8175.1996.tb00863.x.

BACKGROUND: Myocardial reflectivity is abnormally increased in patients with thalassemia major under transfusion treatment, probably due to myocardial iron deposits and/or secondary structural changes. Such increased reflectivity has been detected by both qualitative and subjective analysis of two-dimensional echocardiographic...

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Lattanzi F, Bellotti P, Picano E, et al. Quantitative Texture Analysis in Two-Dimensional Echocardiography: Application to the Diagnosis of Myocardial Hemochromatosis. Echocardiography. 1996;13(1):9-20doi: 10.1111/j.1540-8175.1996.tb00863.x.
Lattanzi, F., Bellotti, P., Picano, E., Chiarella, F., Paterni, M., Forni, G., Landini, L., Distante, A., & Vecchio, C. (1996). Quantitative Texture Analysis in Two-Dimensional Echocardiography: Application to the Diagnosis of Myocardial Hemochromatosis. Echocardiography (Mount Kisco, N.Y.), 13(1), 9-20. https://doi.org/10.1111/j.1540-8175.1996.tb00863.x
Lattanzi, Fabio, et al. "Quantitative Texture Analysis in Two-Dimensional Echocardiography: Application to the Diagnosis of Myocardial Hemochromatosis." Echocardiography (Mount Kisco, N.Y.) vol. 13,1 (1996): 9-20. doi: https://doi.org/10.1111/j.1540-8175.1996.tb00863.x
Lattanzi F, Bellotti P, Picano E, Chiarella F, Paterni M, Forni G, Landini L, Distante A, Vecchio C. Quantitative Texture Analysis in Two-Dimensional Echocardiography: Application to the Diagnosis of Myocardial Hemochromatosis. Echocardiography. 1996 Jan;13(1):9-20. doi: 10.1111/j.1540-8175.1996.tb00863.x. PMID: 11442899.
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Catalytic enantioselective addition of indoles to arylnitroalkenes: an effective route to enantiomerically enriched tryptamine precursors.

Chirality

Bandini M, Garelli A, Rovinetti M, Tommasi S, Umani-Ronchi A.
PMID: 16170793
Chirality. 2005 Nov;17(9):522-9. doi: 10.1002/chir.20189.

A new valuable catalytic protocol for the preparation of synthetically useful beta-indolyl nitro compounds bearing benzhydryl stereocenters is presented. The combined use of catalytic amounts of a commercially available chiral [SalenAlCl] complex and pyridine allowed, for the Friedel-Crafts alkylation...

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Bandini M, Garelli A, Rovinetti M, et al. Catalytic enantioselective addition of indoles to arylnitroalkenes: an effective route to enantiomerically enriched tryptamine precursors. Chirality. 2005;17(9):522-9doi: 10.1002/chir.20189.
Bandini, M., Garelli, A., Rovinetti, M., Tommasi, S., & Umani-Ronchi, A. (2005). Catalytic enantioselective addition of indoles to arylnitroalkenes: an effective route to enantiomerically enriched tryptamine precursors. Chirality, 17(9), 522-9. https://doi.org/10.1002/chir.20189
Bandini, Marco, et al. "Catalytic enantioselective addition of indoles to arylnitroalkenes: an effective route to enantiomerically enriched tryptamine precursors." Chirality vol. 17,9 (2005): 522-9. doi: https://doi.org/10.1002/chir.20189
Bandini M, Garelli A, Rovinetti M, Tommasi S, Umani-Ronchi A. Catalytic enantioselective addition of indoles to arylnitroalkenes: an effective route to enantiomerically enriched tryptamine precursors. Chirality. 2005 Nov;17(9):522-9. doi: 10.1002/chir.20189. PMID: 16170793.
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Recoverable PEG-supported copper catalyst for highly stereocontrolled nitroaldol condensation.

Organic letters

Bandini M, Benaglia M, Sinisi R, Tommasi S, Umani-Ronchi A.
PMID: 17480085
Org Lett. 2007 May 24;9(11):2151-3. doi: 10.1021/ol070636w. Epub 2007 May 05.

A new poly(ethylene glycol)-modified DAT2-Cu(OAc)2 complex smoothly catalyzes a base-free nitroaldol condensation in a highly enantioselective manner (ee up to 93%) also in reagent-grade solvent and in the presence of air. Effective recovery and recycling (up to five runs)...

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Bandini M, Benaglia M, Sinisi R, et al. Recoverable PEG-supported copper catalyst for highly stereocontrolled nitroaldol condensation. Org Lett. 2007;9(11):2151-3doi: 10.1021/ol070636w.
Bandini, M., Benaglia, M., Sinisi, R., Tommasi, S., & Umani-Ronchi, A. (2007). Recoverable PEG-supported copper catalyst for highly stereocontrolled nitroaldol condensation. Organic letters, 9(11), 2151-3. https://doi.org/10.1021/ol070636w
Bandini, Marco, et al. "Recoverable PEG-supported copper catalyst for highly stereocontrolled nitroaldol condensation." Organic letters vol. 9,11 (2007): 2151-3. doi: https://doi.org/10.1021/ol070636w
Bandini M, Benaglia M, Sinisi R, Tommasi S, Umani-Ronchi A. Recoverable PEG-supported copper catalyst for highly stereocontrolled nitroaldol condensation. Org Lett. 2007 May 24;9(11):2151-3. doi: 10.1021/ol070636w. Epub 2007 May 05. PMID: 17480085.
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Synthesis, multiphase characterization, and helicity control in chiral DACH-linked oligothiophenes.

Chemistry (Weinheim an der Bergstrasse, Germany)

Melucci M, Barbarella G, Gazzano M, Cavallini M, Biscarini F, Bongini A, Piccinelli F, Monari M, Bandini M, Umani-Ronchi A, Biscarini P.
PMID: 16944542
Chemistry. 2006 Sep 25;12(28):7305-12. doi: 10.1002/chem.200600312.

A new class of chiral oligothiophenes is described. Mono-, bi-, ter-, and quarterthiophenes have been linked to enantiopure trans-1,2-cyclohexanediamine (DACH) via diamino or diimino moieties. The stereochemistry of DACH, the type of linker, and oligothiophene size determine the conformational...

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Melucci M, Barbarella G, Gazzano M, et al. Synthesis, multiphase characterization, and helicity control in chiral DACH-linked oligothiophenes. Chemistry. 2006;12(28):7305-12doi: 10.1002/chem.200600312.
Melucci, M., Barbarella, G., Gazzano, M., Cavallini, M., Biscarini, F., Bongini, A., Piccinelli, F., Monari, M., Bandini, M., Umani-Ronchi, A., & Biscarini, P. (2006). Synthesis, multiphase characterization, and helicity control in chiral DACH-linked oligothiophenes. Chemistry (Weinheim an der Bergstrasse, Germany), 12(28), 7305-12. https://doi.org/10.1002/chem.200600312
Melucci, Manuela, et al. "Synthesis, multiphase characterization, and helicity control in chiral DACH-linked oligothiophenes." Chemistry (Weinheim an der Bergstrasse, Germany) vol. 12,28 (2006): 7305-12. doi: https://doi.org/10.1002/chem.200600312
Melucci M, Barbarella G, Gazzano M, Cavallini M, Biscarini F, Bongini A, Piccinelli F, Monari M, Bandini M, Umani-Ronchi A, Biscarini P. Synthesis, multiphase characterization, and helicity control in chiral DACH-linked oligothiophenes. Chemistry. 2006 Sep 25;12(28):7305-12. doi: 10.1002/chem.200600312. PMID: 16944542.
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HERSCHEL/SCORE, imaging the solar corona in visible and EUV light: CCD camera characterization.

Analytical and bioanalytical chemistry

Pancrazzi M, Focardi M, Landini F, Romoli M, Fineschi S, Gherardi A, Pace E, Massone G, Antonucci E, Moses D, Newmark J, Wang D, Rossi G.
PMID: 20428852
Anal Bioanal Chem. 2010 Jul;397(6):2033-8. doi: 10.1007/s00216-010-3697-5. Epub 2010 Apr 29.

The HERSCHEL (helium resonant scattering in the corona and heliosphere) experiment is a rocket mission that was successfully launched last September from White Sands Missile Range, New Mexico, USA. HERSCHEL was conceived to investigate the solar corona in the...

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Pancrazzi M, Focardi M, Landini F, et al. HERSCHEL/SCORE, imaging the solar corona in visible and EUV light: CCD camera characterization. Anal Bioanal Chem. 2010;397(6):2033-8doi: 10.1007/s00216-010-3697-5.
Pancrazzi, M., Focardi, M., Landini, F., Romoli, M., Fineschi, S., Gherardi, A., Pace, E., Massone, G., Antonucci, E., Moses, D., Newmark, J., Wang, D., & Rossi, G. (2010). HERSCHEL/SCORE, imaging the solar corona in visible and EUV light: CCD camera characterization. Analytical and bioanalytical chemistry, 397(6), 2033-8. https://doi.org/10.1007/s00216-010-3697-5
Pancrazzi, M, et al. "HERSCHEL/SCORE, imaging the solar corona in visible and EUV light: CCD camera characterization." Analytical and bioanalytical chemistry vol. 397,6 (2010): 2033-8. doi: https://doi.org/10.1007/s00216-010-3697-5
Pancrazzi M, Focardi M, Landini F, Romoli M, Fineschi S, Gherardi A, Pace E, Massone G, Antonucci E, Moses D, Newmark J, Wang D, Rossi G. HERSCHEL/SCORE, imaging the solar corona in visible and EUV light: CCD camera characterization. Anal Bioanal Chem. 2010 Jul;397(6):2033-8. doi: 10.1007/s00216-010-3697-5. Epub 2010 Apr 29. PMID: 20428852.
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Showing 1 to 12 of 449 entries