Advanced Search
Display options
Filter resources
Text Availability
Article type
Publication date
Species
Language
Sex
Age
Showing 1 to 12 of 283 entries
Sorted by: Best Match Show Resources per page
Effectiveness of interventions to improve patient compliance: a meta-analysis

interventions

Roter DL, Hall JA.
GSID: 3__Yf-cvGYIJ
DL Roter, JA Hall, R Merisca, B Nordstrom, D Cretin… - Medical care, 1998 - JSTOR

… interventions, 32 evaluated three different interventions, and 10 presented analysis of four or more different compliance interventions. … For interventions with a single primary programmatic focus, educational interventions (n = 50) were somewhat more frequent than behav…

Cite
Roter, D. L., Hall, J. A., Merisca, R., Nordstrom, B., Cretin, D., & Svarstad, B. (1998). Effectiveness of interventions to improve patient compliance: a meta-analysis. Medical care, 1138-1161.
Roter, Debra L., et al. "Effectiveness of interventions to improve patient compliance: a meta-analysis." Medical care (1998): 1138-1161.
Copy Download .nbib Format: MLA
Patient-provider communication: the effect of race and ethnicity on process and outcomes of healthcare

Minority STEM training

Cooper LA, Roter DL.
GSID: S8GkC8WA1FgJ
LA Cooper, DL Roter - … racial and ethnic disparities in health care, 2003 - europepmc.org

… we must rely on physician training in interpersonal skills that … no differences between ethnic minority and white physicians … health, and although this has usually been assumed to stem …

Cite
Cooper, L. A., & Roter, D. L. (2003). Patient-provider communication: the effect of race and ethnicity on process and outcomes of healthcare. Unequal treatment: Confronting racial and ethnic disparities in health care, 552-93.
Cooper, Lisa A., and Debra L. Roter. "Patient-provider communication: the effect of race and ethnicity on process and outcomes of healthcare." Unequal treatment: Confronting racial and ethnic disparities in health care (2003): 552-93.
Copy Download .nbib Format: MLA
Editorial.

Bioorganic & medicinal chemistry letters

Boger DL.
PMID: 26343827
Bioorg Med Chem Lett. 2015 Nov 01;25(21):4713. doi: 10.1016/j.bmcl.2015.08.082. Epub 2015 Sep 01.

No abstract available.

Cite
Boger DL. Editorial. Bioorg Med Chem Lett. 2015;25(21):4713doi: 10.1016/j.bmcl.2015.08.082.
Boger, D. L. (2015). Editorial. Bioorganic & medicinal chemistry letters, 25(21), 4713. https://doi.org/10.1016/j.bmcl.2015.08.082
Boger, Dale L. "Editorial." Bioorganic & medicinal chemistry letters vol. 25,21 (2015): 4713. doi: https://doi.org/10.1016/j.bmcl.2015.08.082
Boger DL. Editorial. Bioorg Med Chem Lett. 2015 Nov 01;25(21):4713. doi: 10.1016/j.bmcl.2015.08.082. Epub 2015 Sep 01. PMID: 26343827.
Copy Download .nbib Format: NLM
Critical Issues in the Understanding of Young Elementary School Students at Risk for Problems in Written Expression: Introduction to the Special Series.

Journal of learning disabilities

Coker DL, Kim YG.
PMID: 28498735
J Learn Disabil. 2018 Jul/Aug;51(4):315-319. doi: 10.1177/0022219417708168. Epub 2017 May 12.

In this introduction to the special series "Critical Issues in the Understanding of Young Elementary School Students at Risk for Problems in Written Expression," we consider some of the contextual factors that have changed since a similar special issue...

Cite
Coker DL, Kim YG. Critical Issues in the Understanding of Young Elementary School Students at Risk for Problems in Written Expression: Introduction to the Special Series. J Learn Disabil. 2017;51(4):315-319doi: 10.1177/0022219417708168.
Coker, D. L., & Kim, Y. G. (2018). Critical Issues in the Understanding of Young Elementary School Students at Risk for Problems in Written Expression: Introduction to the Special Series. Journal of learning disabilities, 51(4), 315-319. https://doi.org/10.1177/0022219417708168
Coker, David L, and Kim, Young-Suk Grace. "Critical Issues in the Understanding of Young Elementary School Students at Risk for Problems in Written Expression: Introduction to the Special Series." Journal of learning disabilities vol. 51,4 (2018): 315-319. doi: https://doi.org/10.1177/0022219417708168
Coker DL, Kim YG. Critical Issues in the Understanding of Young Elementary School Students at Risk for Problems in Written Expression: Introduction to the Special Series. J Learn Disabil. 2018 Jul/Aug;51(4):315-319. doi: 10.1177/0022219417708168. Epub 2017 May 12. PMID: 28498735.
Copy Download .nbib Format: NLM
Syntheses, structural, magnetic, and electron paramagnetic resonance studies of monobridged cyanide and azide dinuclear copper(II) complexes: antiferromagnetic superexchange interactions.

Inorganic chemistry

Reger DL, Pascui AE, Smith MD, Jezierska J, Ozarowski A.
PMID: 25602445
Inorg Chem. 2015 Feb 16;54(4):1487-500. doi: 10.1021/ic502485p. Epub 2015 Jan 20.

The reactions of Cu(ClO4)2 with NaCN and the ditopic ligands m-bis[bis(1-pyrazolyl)methyl]benzene (Lm) or m-bis[bis(3,5-dimethyl-1-pyrazolyl)methyl]benzene (Lm*) yield [Cu2(μ-CN)(μ-Lm)2](ClO4)3 (1) and [Cu2(μ-CN)(μ-Lm*)2](ClO4)3 (3). In both, the cyanide ligand is linearly bridged (μ-1,2) leading to a separation of the two copper(II) ions...

Cite
Reger DL, Pascui AE, Smith MD, et al. Syntheses, structural, magnetic, and electron paramagnetic resonance studies of monobridged cyanide and azide dinuclear copper(II) complexes: antiferromagnetic superexchange interactions. Inorg Chem. 2015;54(4):1487-500doi: 10.1021/ic502485p.
Reger, D. L., Pascui, A. E., Smith, M. D., Jezierska, J., & Ozarowski, A. (2015). Syntheses, structural, magnetic, and electron paramagnetic resonance studies of monobridged cyanide and azide dinuclear copper(II) complexes: antiferromagnetic superexchange interactions. Inorganic chemistry, 54(4), 1487-500. https://doi.org/10.1021/ic502485p
Reger, Daniel L, et al. "Syntheses, structural, magnetic, and electron paramagnetic resonance studies of monobridged cyanide and azide dinuclear copper(II) complexes: antiferromagnetic superexchange interactions." Inorganic chemistry vol. 54,4 (2015): 1487-500. doi: https://doi.org/10.1021/ic502485p
Reger DL, Pascui AE, Smith MD, Jezierska J, Ozarowski A. Syntheses, structural, magnetic, and electron paramagnetic resonance studies of monobridged cyanide and azide dinuclear copper(II) complexes: antiferromagnetic superexchange interactions. Inorg Chem. 2015 Feb 16;54(4):1487-500. doi: 10.1021/ic502485p. Epub 2015 Jan 20. PMID: 25602445.
Copy Download .nbib Format: NLM
Corrigendum: Three keys to the radiation of angiosperms into freezing environments.

Nature

Zanne AE, Tank DC, Cornwell WK, Eastman JM, Smith SA, FitzJohn RG, McGlinn DJ, O'Meara BC, Moles AT, Reich PB, Royer DL, Soltis DE, Stevens PF, Westoby M, Wright IJ, Aarssen L, Bertin RI, Calaminus A, Govaerts R, Hemmings F, Leishman MR, Oleksyn J, Soltis PS, Swenson NG, Warman L, Beaulieu JM.
PMID: 25993966
Nature. 2015 May 21;521(7552):380. doi: 10.1038/nature14371.

No abstract available.

Cite
Zanne AE, Tank DC, Cornwell WK, et al. Corrigendum: Three keys to the radiation of angiosperms into freezing environments. Nature. 2015;521(7552):380doi: 10.1038/nature14371.
Zanne, A. E., Tank, D. C., Cornwell, W. K., Eastman, J. M., Smith, S. A., FitzJohn, R. G., McGlinn, D. J., O'Meara, B. C., Moles, A. T., Reich, P. B., Royer, D. L., Soltis, D. E., Stevens, P. F., Westoby, M., Wright, I. J., Aarssen, L., Bertin, R. I., Calaminus, A., Govaerts, R., Hemmings, F., Leishman, M. R., Oleksyn, J., Soltis, P. S., Swenson, N. G., Warman, L., & Beaulieu, J. M. (2015). Corrigendum: Three keys to the radiation of angiosperms into freezing environments. Nature, 521(7552), 380. https://doi.org/10.1038/nature14371
Zanne, Amy E, et al. "Corrigendum: Three keys to the radiation of angiosperms into freezing environments." Nature vol. 521,7552 (2015): 380. doi: https://doi.org/10.1038/nature14371
Zanne AE, Tank DC, Cornwell WK, Eastman JM, Smith SA, FitzJohn RG, McGlinn DJ, O'Meara BC, Moles AT, Reich PB, Royer DL, Soltis DE, Stevens PF, Westoby M, Wright IJ, Aarssen L, Bertin RI, Calaminus A, Govaerts R, Hemmings F, Leishman MR, Oleksyn J, Soltis PS, Swenson NG, Warman L, Beaulieu JM. Corrigendum: Three keys to the radiation of angiosperms into freezing environments. Nature. 2015 May 21;521(7552):380. doi: 10.1038/nature14371. PMID: 25993966.
Copy Download .nbib Format: NLM
Total Synthesis of Quinoxapeptin A-C: Establishment of Absolute Stereochemistry.

Angewandte Chemie (International ed. in English)

Boger DL, Ledeboer MW, Kume M, Jin Q.
PMID: 10458810
Angew Chem Int Ed Engl. 1999 Aug;38(16):2424-2426. doi: 10.1002/(sici)1521-3773(19990816)38:16<2424::aid-anie2424>3.0.co;2-9.

The relative and absolute stereochemistry of the naturally occurring potent HIV reverse transcriptase (RT) inhibitors 1 and 2, quinoxapeptin A and B, were established by total synthesis. Their synthetic precursor 3 (dubbed quinoxapeptin C) was found to be a...

Cite
Boger DL, Ledeboer MW, Kume M, et al. Total Synthesis of Quinoxapeptin A-C: Establishment of Absolute Stereochemistry. Angew Chem Int Ed Engl. 1999;38(16):2424-2426doi: 10.1002/(sici)1521-3773(19990816)38:16<2424::aid-anie2424>3.0.co;2-9.
Boger, D. L., Ledeboer, M. W., Kume, M., & Jin, Q. (1999). Total Synthesis of Quinoxapeptin A-C: Establishment of Absolute Stereochemistry. Angewandte Chemie (International ed. in English), 38(16), 2424-2426. https://doi.org/10.1002/(sici)1521-3773(19990816)38:16<2424::aid-anie2424>3.0.co;2-9
Boger, et al. "Total Synthesis of Quinoxapeptin A-C: Establishment of Absolute Stereochemistry." Angewandte Chemie (International ed. in English) vol. 38,16 (1999): 2424-2426. doi: https://doi.org/10.1002/(sici)1521-3773(19990816)38:16<2424::aid-anie2424>3.0.co;2-9
Boger DL, Ledeboer MW, Kume M, Jin Q. Total Synthesis of Quinoxapeptin A-C: Establishment of Absolute Stereochemistry. Angew Chem Int Ed Engl. 1999 Aug;38(16):2424-2426. doi: 10.1002/(sici)1521-3773(19990816)38:16<2424::aid-anie2424>3.0.co;2-9. PMID: 10458810.
Copy Download .nbib Format: NLM
A Six-Coordinate Tris(3,5-dimethyl-1-pyrazolyl)methane-Thallium(I) Complex with a Stereochemically Inactive Lone Pair: Syntheses and Solid State Structures of {[HC(3,5-Me(2)pz)(3)](2)Tl}PF(6) and {[HC(3,5-Me(2)pz)(3)]Tl}PF(6) (pz = Pyrazolyl).

Inorganic chemistry

Reger DL, Collins JE, Layland R, Adams RD.
PMID: 11666335
Inorg Chem. 1996 Feb 28;35(5):1372-1376. doi: 10.1021/ic951167+.

The addition of the tris(pyrazolyl)methane ligand HC(3,5-Me(2)pz)(3) (pz = pyrazolyl ring) to a THF solution of TlPF(6) results in the immediate precipitation of {[HC(3,5-Me(2)pz)(3)](2)Tl}PF(6). The structure has been determined crystallographically. The arrangement of the nitrogen donor atoms about the...

Cite
Reger DL, Collins JE, Layland R, et al. A Six-Coordinate Tris(3,5-dimethyl-1-pyrazolyl)methane-Thallium(I) Complex with a Stereochemically Inactive Lone Pair: Syntheses and Solid State Structures of {[HC(3,5-Me(2)pz)(3)](2)Tl}PF(6) and {[HC(3,5-Me(2)pz)(3)]Tl}PF(6) (pz = Pyrazolyl). Inorg Chem. 1996;35(5):1372-1376doi: 10.1021/ic951167+.
Reger, D. L., Collins, J. E., Layland, R., & Adams, R. D. (1996). A Six-Coordinate Tris(3,5-dimethyl-1-pyrazolyl)methane-Thallium(I) Complex with a Stereochemically Inactive Lone Pair: Syntheses and Solid State Structures of {[HC(3,5-Me(2)pz)(3)](2)Tl}PF(6) and {[HC(3,5-Me(2)pz)(3)]Tl}PF(6) (pz = Pyrazolyl). Inorganic chemistry, 35(5), 1372-1376. https://doi.org/10.1021/ic951167+
Reger, Daniel L., et al. "A Six-Coordinate Tris(3,5-dimethyl-1-pyrazolyl)methane-Thallium(I) Complex with a Stereochemically Inactive Lone Pair: Syntheses and Solid State Structures of {[HC(3,5-Me(2)pz)(3)](2)Tl}PF(6) and {[HC(3,5-Me(2)pz)(3)]Tl}PF(6) (pz = Pyrazolyl)." Inorganic chemistry vol. 35,5 (1996): 1372-1376. doi: https://doi.org/10.1021/ic951167+
Reger DL, Collins JE, Layland R, Adams RD. A Six-Coordinate Tris(3,5-dimethyl-1-pyrazolyl)methane-Thallium(I) Complex with a Stereochemically Inactive Lone Pair: Syntheses and Solid State Structures of {[HC(3,5-Me(2)pz)(3)](2)Tl}PF(6) and {[HC(3,5-Me(2)pz)(3)]Tl}PF(6) (pz = Pyrazolyl). Inorg Chem. 1996 Feb 28;35(5):1372-1376. doi: 10.1021/ic951167+. PMID: 11666335.
Copy Download .nbib Format: NLM
Supramolecular structures of cadmium(II) coordination polymers: a new class of ligands formed by linking tripodal tris(pyrazolyl)methane units.

Inorganic chemistry

Reger DL, Wright TD, Semeniuc RF, Grattan TC, Smith MD.
PMID: 11703122
Inorg Chem. 2001 Nov 19;40(24):6212-9. doi: 10.1021/ic010574k.

The new ligands C(6)H(4)[CH(2)OCH(2)C(pz)(3)](2) (pz = pyrazolyl ring), 1 (ortho), 2 (meta), and 3 (para), that can potentially bond two or more metal centers were obtained in a single step from the reaction of the appropriate dibromoxylene, 2 equiv...

Cite
Reger DL, Wright TD, Semeniuc RF, et al. Supramolecular structures of cadmium(II) coordination polymers: a new class of ligands formed by linking tripodal tris(pyrazolyl)methane units. Inorg Chem. 2001;40(24):6212-9doi: 10.1021/ic010574k.
Reger, D. L., Wright, T. D., Semeniuc, R. F., Grattan, T. C., & Smith, M. D. (2001). Supramolecular structures of cadmium(II) coordination polymers: a new class of ligands formed by linking tripodal tris(pyrazolyl)methane units. Inorganic chemistry, 40(24), 6212-9. https://doi.org/10.1021/ic010574k
Reger, D L, et al. "Supramolecular structures of cadmium(II) coordination polymers: a new class of ligands formed by linking tripodal tris(pyrazolyl)methane units." Inorganic chemistry vol. 40,24 (2001): 6212-9. doi: https://doi.org/10.1021/ic010574k
Reger DL, Wright TD, Semeniuc RF, Grattan TC, Smith MD. Supramolecular structures of cadmium(II) coordination polymers: a new class of ligands formed by linking tripodal tris(pyrazolyl)methane units. Inorg Chem. 2001 Nov 19;40(24):6212-9. doi: 10.1021/ic010574k. PMID: 11703122.
Copy Download .nbib Format: NLM
Are the Duocarmycin and CC-1065 DNA Alkylation Reactions Acid-Catalyzed? Solvolysis pH-Rate Profiles Suggest They Are Not.

The Journal of organic chemistry

Boger DL, Garbaccio RM.
PMID: 11674637
J Org Chem. 1999 Jul 23;64(15):5666-5669. doi: 10.1021/jo990762g.

A study of the solvolysis pH-rate profiles for two key reactive CC-1065/duocarmycin alkylation subunit analogues is detailed. Unlike the authentic alkylation subunits and N-BOC-CBI (4) which are too stable to establish complete solvolysis pH-rate profiles, the analogues N-BOC-CBQ (5)...

Cite
Boger DL, Garbaccio RM. Are the Duocarmycin and CC-1065 DNA Alkylation Reactions Acid-Catalyzed? Solvolysis pH-Rate Profiles Suggest They Are Not. J Org Chem. 1999;64(15):5666-5669doi: 10.1021/jo990762g.
Boger, D. L., & Garbaccio, R. M. (1999). Are the Duocarmycin and CC-1065 DNA Alkylation Reactions Acid-Catalyzed? Solvolysis pH-Rate Profiles Suggest They Are Not. The Journal of organic chemistry, 64(15), 5666-5669. https://doi.org/10.1021/jo990762g
Boger, Dale L., and Garbaccio, Robert M.. "Are the Duocarmycin and CC-1065 DNA Alkylation Reactions Acid-Catalyzed? Solvolysis pH-Rate Profiles Suggest They Are Not." The Journal of organic chemistry vol. 64,15 (1999): 5666-5669. doi: https://doi.org/10.1021/jo990762g
Boger DL, Garbaccio RM. Are the Duocarmycin and CC-1065 DNA Alkylation Reactions Acid-Catalyzed? Solvolysis pH-Rate Profiles Suggest They Are Not. J Org Chem. 1999 Jul 23;64(15):5666-5669. doi: 10.1021/jo990762g. PMID: 11674637.
Copy Download .nbib Format: NLM
CC-1065 and the Duocarmycins: Synthetic Studies.

Chemical reviews

Boger DL, Boyce CW, Garbaccio RM, Goldberg JA.
PMID: 11848889
Chem Rev. 1997 May 08;97(3):787-828. doi: 10.1021/cr960095g.

No abstract available.

Cite
Boger DL, Boyce CW, Garbaccio RM, et al. CC-1065 and the Duocarmycins: Synthetic Studies. Chem Rev. 1997;97(3):787-828doi: 10.1021/cr960095g.
Boger, D. L., Boyce, C. W., Garbaccio, R. M., & Goldberg, J. A. (1997). CC-1065 and the Duocarmycins: Synthetic Studies. Chemical reviews, 97(3), 787-828. https://doi.org/10.1021/cr960095g
Boger, Dale L., et al. "CC-1065 and the Duocarmycins: Synthetic Studies." Chemical reviews vol. 97,3 (1997): 787-828. doi: https://doi.org/10.1021/cr960095g
Boger DL, Boyce CW, Garbaccio RM, Goldberg JA. CC-1065 and the Duocarmycins: Synthetic Studies. Chem Rev. 1997 May 08;97(3):787-828. doi: 10.1021/cr960095g. PMID: 11848889.
Copy Download .nbib Format: NLM
A stereoselective intramolecular 1,3-dipolar nitrone cycloaddition for the synthesis of substituted chromanes.

The Journal of organic chemistry

Zhao Q, Han F, Romero DL.
PMID: 12003541
J Org Chem. 2002 May 17;67(10):3317-22. doi: 10.1021/jo011015y.

A stereoselective intramolecular 1,3-dipolar nitrone cycloaddition useful in the synthesis of chromanes is described. The reaction relies on the use of a chiral auxiliary on the nitrone partner. Key to the success of the reaction is the choice of...

Cite
Zhao Q, Han F, Romero DL. A stereoselective intramolecular 1,3-dipolar nitrone cycloaddition for the synthesis of substituted chromanes. J Org Chem. 2002;67(10):3317-22doi: 10.1021/jo011015y.
Zhao, Q., Han, F., & Romero, D. L. (2002). A stereoselective intramolecular 1,3-dipolar nitrone cycloaddition for the synthesis of substituted chromanes. The Journal of organic chemistry, 67(10), 3317-22. https://doi.org/10.1021/jo011015y
Zhao, Qian, et al. "A stereoselective intramolecular 1,3-dipolar nitrone cycloaddition for the synthesis of substituted chromanes." The Journal of organic chemistry vol. 67,10 (2002): 3317-22. doi: https://doi.org/10.1021/jo011015y
Zhao Q, Han F, Romero DL. A stereoselective intramolecular 1,3-dipolar nitrone cycloaddition for the synthesis of substituted chromanes. J Org Chem. 2002 May 17;67(10):3317-22. doi: 10.1021/jo011015y. PMID: 12003541.
Copy Download .nbib Format: NLM
Showing 1 to 12 of 283 entries