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Workforce diversity training: From anti-discrimination compliance to organizational development

workforce diversity

Bendick M.
GSID: 930IBGaA5kwJ
M Bendick Jr, ML Egan… - Human Resource …, 2001 - search.ebscohost.com

… nation and workforce diversity encompasses a variety of approaches. Many training programs focus on itidividual attitudes and appear to have … adopting this final approach appear to be the tnost effective, they are commonly implemented by only 23...

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Bendick Jr, M., Egan, M. L., & Lofhjelm, S. M. (2001). Workforce diversity training: From anti-discrimination compliance to organizational development. Human Resource Planning, 24(2).
Bendick Jr, Marc, Mary Lou Egan, and Suzanne M. Lofhjelm. "Workforce diversity training: From anti-discrimination compliance to organizational development." Human Resource Planning 24.2 (2001).
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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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Differential scanning calorimeter application to the detectionof refined hazelnut oil in extra virgin olive oil.

Food chemistry

Chiavaro E, Vittadini E, Rodriguez-Estrada MT, Cerretani L, Bendini A.
PMID: 26050190
Food Chem. 2008 Sep 01;110(1):248-56. doi: 10.1016/j.foodchem.2008.01.044. Epub 2008 Feb 02.

The potential application of differential scanning calorimetry (DSC) to verify adulteration of extra virgin olive oil with refined hazelnut oil was evaluated. Extra virgin olive oil and hazelnut oil were characterised by significantly different cooling and heating DSC thermal...

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Chiavaro E, Vittadini E, Rodriguez-Estrada MT, et al. Differential scanning calorimeter application to the detectionof refined hazelnut oil in extra virgin olive oil. Food Chem. 2008;110(1):248-56doi: 10.1016/j.foodchem.2008.01.044.
Chiavaro, E., Vittadini, E., Rodriguez-Estrada, M. T., Cerretani, L., & Bendini, A. (2008). Differential scanning calorimeter application to the detectionof refined hazelnut oil in extra virgin olive oil. Food chemistry, 110(1), 248-56. https://doi.org/10.1016/j.foodchem.2008.01.044
Chiavaro, Emma, et al. "Differential scanning calorimeter application to the detectionof refined hazelnut oil in extra virgin olive oil." Food chemistry vol. 110,1 (2008): 248-56. doi: https://doi.org/10.1016/j.foodchem.2008.01.044
Chiavaro E, Vittadini E, Rodriguez-Estrada MT, Cerretani L, Bendini A. Differential scanning calorimeter application to the detectionof refined hazelnut oil in extra virgin olive oil. Food Chem. 2008 Sep 01;110(1):248-56. doi: 10.1016/j.foodchem.2008.01.044. Epub 2008 Feb 02. PMID: 26050190.
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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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Ultimate Limit in the Spectral Resolution of Extreme Ultraviolet Frequency Combs.

Physical review letters

Corsi C, Liontos I, Bellini M, Cavalieri S, Cancio Pastor P, Siciliani de Cumis M, Eramo R.
PMID: 28430481
Phys Rev Lett. 2017 Apr 07;118(14):143201. doi: 10.1103/PhysRevLett.118.143201. Epub 2017 Apr 03.

We present the results of direct interferometric measurements on the pulse-to-pulse phase jitter of a metrological, fiber-based, infrared (IR) frequency comb. We show that the short-time evolution of such phase fluctuations, which cannot be actively controlled by any feedback...

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Corsi C, Liontos I, Bellini M, et al. Ultimate Limit in the Spectral Resolution of Extreme Ultraviolet Frequency Combs. Phys Rev Lett. 2017;118(14):143201doi: 10.1103/PhysRevLett.118.143201.
Corsi, C., Liontos, I., Bellini, M., Cavalieri, S., Cancio Pastor, P., Siciliani de Cumis, M., & Eramo, R. (2017). Ultimate Limit in the Spectral Resolution of Extreme Ultraviolet Frequency Combs. Physical review letters, 118(14), 143201. https://doi.org/10.1103/PhysRevLett.118.143201
Corsi, C, et al. "Ultimate Limit in the Spectral Resolution of Extreme Ultraviolet Frequency Combs." Physical review letters vol. 118,14 (2017): 143201. doi: https://doi.org/10.1103/PhysRevLett.118.143201
Corsi C, Liontos I, Bellini M, Cavalieri S, Cancio Pastor P, Siciliani de Cumis M, Eramo R. Ultimate Limit in the Spectral Resolution of Extreme Ultraviolet Frequency Combs. Phys Rev Lett. 2017 Apr 07;118(14):143201. doi: 10.1103/PhysRevLett.118.143201. Epub 2017 Apr 03. PMID: 28430481.
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A fluorescent receptor for halide recognition: clues for the design of anion chemosensors.

Physical chemistry chemical physics : PCCP

Chelli R, Pietraperzia G, Bencini A, Giorgi C, Lippolis V, Salvi PR, Gellini C.
PMID: 25814174
Phys Chem Chem Phys. 2015 Apr 28;17(16):10813-22. doi: 10.1039/c5cp00131e.

The chemosensing properties of the polyaza-macrocycle 1-(6,7)-acridine-3,6,9,12-tetraaza-tridecaphane have been investigated by means of emission fluorescence spectroscopy, considering halide ions as substrates. As in the case of the free ligand, the fluorescence emission of the complexes is due to the...

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Chelli R, Pietraperzia G, Bencini A, et al. A fluorescent receptor for halide recognition: clues for the design of anion chemosensors. Phys Chem Chem Phys. 2015;17(16):10813-22doi: 10.1039/c5cp00131e.
Chelli, R., Pietraperzia, G., Bencini, A., Giorgi, C., Lippolis, V., Salvi, P. R., & Gellini, C. (2015). A fluorescent receptor for halide recognition: clues for the design of anion chemosensors. Physical chemistry chemical physics : PCCP, 17(16), 10813-22. https://doi.org/10.1039/c5cp00131e
Chelli, Riccardo, et al. "A fluorescent receptor for halide recognition: clues for the design of anion chemosensors." Physical chemistry chemical physics : PCCP vol. 17,16 (2015): 10813-22. doi: https://doi.org/10.1039/c5cp00131e
Chelli R, Pietraperzia G, Bencini A, Giorgi C, Lippolis V, Salvi PR, Gellini C. A fluorescent receptor for halide recognition: clues for the design of anion chemosensors. Phys Chem Chem Phys. 2015 Apr 28;17(16):10813-22. doi: 10.1039/c5cp00131e. PMID: 25814174.
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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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High performance computing enabling exhaustive analysis of higher order single nucleotide polymorphism interaction in Genome Wide Association Studies.

Health information science and systems

Goudey B, Abedini M, Hopper JL, Inouye M, Makalic E, Schmidt DF, Wagner J, Zhou Z, Zobel J, Reumann M.
PMID: 25870758
Health Inf Sci Syst. 2015 Feb 24;3:S3. doi: 10.1186/2047-2501-3-S1-S3. eCollection 2015.

Genome-wide association studies (GWAS) are a common approach for systematic discovery of single nucleotide polymorphisms (SNPs) which are associated with a given disease. Univariate analysis approaches commonly employed may miss important SNP associations that only appear through multivariate analysis...

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Goudey B, Abedini M, Hopper JL, et al. High performance computing enabling exhaustive analysis of higher order single nucleotide polymorphism interaction in Genome Wide Association Studies. Health Inf Sci Syst. 2015;3:S3doi: 10.1186/2047-2501-3-S1-S3.
Goudey, B., Abedini, M., Hopper, J. L., Inouye, M., Makalic, E., Schmidt, D. F., Wagner, J., Zhou, Z., Zobel, J., & Reumann, M. (2015). High performance computing enabling exhaustive analysis of higher order single nucleotide polymorphism interaction in Genome Wide Association Studies. Health information science and systems, 3S3. https://doi.org/10.1186/2047-2501-3-S1-S3
Goudey, Benjamin, et al. "High performance computing enabling exhaustive analysis of higher order single nucleotide polymorphism interaction in Genome Wide Association Studies." Health information science and systems vol. 3 (2015): S3. doi: https://doi.org/10.1186/2047-2501-3-S1-S3
Goudey B, Abedini M, Hopper JL, Inouye M, Makalic E, Schmidt DF, Wagner J, Zhou Z, Zobel J, Reumann M. High performance computing enabling exhaustive analysis of higher order single nucleotide polymorphism interaction in Genome Wide Association Studies. Health Inf Sci Syst. 2015 Feb 24;3:S3. doi: 10.1186/2047-2501-3-S1-S3. eCollection 2015. PMID: 25870758; PMCID: PMC4383059.
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Spin-Density Map of the Triplet Ground State of a Titanium(IV) Complex with Schiff-Base Diquinone Radical Ligands: An Investigation Using Polarized-Neutron Diffraction and Density-Functional Theory This work was supported by the 3MD EU network (contract ERB 4061 PL 97-0197).

Angewandte Chemie (International ed. in English)

Pontillon Y, Bencini A, Caneschi A, Dei A, Gatteschi D, Gillon B, Sangregorio C, Stride J, Totti F.
PMID: 10934361
Angew Chem Int Ed Engl. 2000 May 15;39(10):1786-1788. doi: 10.1002/(sici)1521-3773(20000515)39:10<1786::aid-anie1786>3.0.co;2-i.

No abstract available.

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Pontillon Y, Bencini A, Caneschi A, et al. Spin-Density Map of the Triplet Ground State of a Titanium(IV) Complex with Schiff-Base Diquinone Radical Ligands: An Investigation Using Polarized-Neutron Diffraction and Density-Functional Theory This work was supported by the 3MD EU network (contract ERB 4061 PL 97-0197). Angew Chem Int Ed Engl. 2000;39(10):1786-1788doi: 10.1002/(sici)1521-3773(20000515)39:10<1786::aid-anie1786>3.0.co;2-i.
Pontillon, Y., Bencini, A., Caneschi, A., Dei, A., Gatteschi, D., Gillon, B., Sangregorio, C., Stride, J., & Totti, F. (2000). Spin-Density Map of the Triplet Ground State of a Titanium(IV) Complex with Schiff-Base Diquinone Radical Ligands: An Investigation Using Polarized-Neutron Diffraction and Density-Functional Theory This work was supported by the 3MD EU network (contract ERB 4061 PL 97-0197). Angewandte Chemie (International ed. in English), 39(10), 1786-1788. https://doi.org/10.1002/(sici)1521-3773(20000515)39:10<1786::aid-anie1786>3.0.co;2-i
Pontillon, et al. "Spin-Density Map of the Triplet Ground State of a Titanium(IV) Complex with Schiff-Base Diquinone Radical Ligands: An Investigation Using Polarized-Neutron Diffraction and Density-Functional Theory This work was supported by the 3MD EU network (contract ERB 4061 PL 97-0197)." Angewandte Chemie (International ed. in English) vol. 39,10 (2000): 1786-1788. doi: https://doi.org/10.1002/(sici)1521-3773(20000515)39:10<1786::aid-anie1786>3.0.co;2-i
Pontillon Y, Bencini A, Caneschi A, Dei A, Gatteschi D, Gillon B, Sangregorio C, Stride J, Totti F. Spin-Density Map of the Triplet Ground State of a Titanium(IV) Complex with Schiff-Base Diquinone Radical Ligands: An Investigation Using Polarized-Neutron Diffraction and Density-Functional Theory This work was supported by the 3MD EU network (contract ERB 4061 PL 97-0197). Angew Chem Int Ed Engl. 2000 May 15;39(10):1786-1788. doi: 10.1002/(sici)1521-3773(20000515)39:10<1786::aid-anie1786>3.0.co;2-i. PMID: 10934361.
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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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Carboxy and Phosphate Esters Cleavage with Mono- and Dinuclear Zinc(II) Macrocyclic Complexes in Aqueous Solution. Crystal Structure of [Zn(2)L1(&mgr;-PP)(2)(MeOH)(2)](ClO(4))(2) (L1 = [30]aneN(6)O(4), PP(-) = Diphenyl Phosphate).

Inorganic chemistry

Bazzicalupi C, Bencini A, Bianchi A, Fusi V, Giorgi C, Paoletti P, Valtancoli B, Zanchi D.
PMID: 11669912
Inorg Chem. 1997 Jun 18;36(13):2784-2790. doi: 10.1021/ic961521j.

The ligand [30]aneN(6)O(4) (L1) binds two Zn(II) in aqueous solution. The stability constants of the L1 complexes have been determined at 308.1 K by means of potentiometric measurements. Dinuclear monohydroxo [Zn(2)L1OH](3+) and dihydroxo [Zn(2)L1(OH)(2)](2+) complexes are formed in aqueous...

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Bazzicalupi C, Bencini A, Bianchi A, et al. Carboxy and Phosphate Esters Cleavage with Mono- and Dinuclear Zinc(II) Macrocyclic Complexes in Aqueous Solution. Crystal Structure of [Zn(2)L1(&mgr;-PP)(2)(MeOH)(2)](ClO(4))(2) (L1 = [30]aneN(6)O(4), PP(-) = Diphenyl Phosphate). Inorg Chem. 1997;36(13):2784-2790doi: 10.1021/ic961521j.
Bazzicalupi, C., Bencini, A., Bianchi, A., Fusi, V., Giorgi, C., Paoletti, P., Valtancoli, B., & Zanchi, D. (1997). Carboxy and Phosphate Esters Cleavage with Mono- and Dinuclear Zinc(II) Macrocyclic Complexes in Aqueous Solution. Crystal Structure of [Zn(2)L1(&mgr;-PP)(2)(MeOH)(2)](ClO(4))(2) (L1 = [30]aneN(6)O(4), PP(-) = Diphenyl Phosphate). Inorganic chemistry, 36(13), 2784-2790. https://doi.org/10.1021/ic961521j
Bazzicalupi, Carla, et al. "Carboxy and Phosphate Esters Cleavage with Mono- and Dinuclear Zinc(II) Macrocyclic Complexes in Aqueous Solution. Crystal Structure of [Zn(2)L1(&mgr;-PP)(2)(MeOH)(2)](ClO(4))(2) (L1 = [30]aneN(6)O(4), PP(-) = Diphenyl Phosphate)." Inorganic chemistry vol. 36,13 (1997): 2784-2790. doi: https://doi.org/10.1021/ic961521j
Bazzicalupi C, Bencini A, Bianchi A, Fusi V, Giorgi C, Paoletti P, Valtancoli B, Zanchi D. Carboxy and Phosphate Esters Cleavage with Mono- and Dinuclear Zinc(II) Macrocyclic Complexes in Aqueous Solution. Crystal Structure of [Zn(2)L1(&mgr;-PP)(2)(MeOH)(2)](ClO(4))(2) (L1 = [30]aneN(6)O(4), PP(-) = Diphenyl Phosphate). Inorg Chem. 1997 Jun 18;36(13):2784-2790. doi: 10.1021/ic961521j. PMID: 11669912.
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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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