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Showing 1 to 12 of 299 entries
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Occupant evaluation of commercial office lighting: Volume 2, Preliminary data analysis

field stations

Brown MA, Marans RW.
GSID: E5Kqgl9Co_4J
RW Marans, MA Brown - 1987 - osti.gov

This report presents the preliminary results of a post-occupancy evaluation of office lighting environments. It explores the relationship between quantitative measures of lighting in …

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Marans, R. W., & Brown, M. A. (1987). Occupant evaluation of commercial office lighting: Volume 2, Preliminary data analysis (No. ORNL/TM-10264/V2). Michigan Univ., Ann Arbor (USA).
Marans, Robert W., and Marilyn A. Brown. Occupant evaluation of commercial office lighting: Volume 2, Preliminary data analysis. No. ORNL/TM-10264/V2. Michigan Univ., Ann Arbor (USA), 1987.
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Budgeting for beginners: outstanding commitments.

Nursing times

Bryans W.
PMID: 3853195
Nurs Times. 1985 Dec 11-17;81(50):40-2.

No abstract available.

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Bryans W. Budgeting for beginners: outstanding commitments. Nurs Times. 1985;81(50):40-2
Bryans, W. (1985). Budgeting for beginners: outstanding commitments. Nursing times, 81(50), 40-2.
Bryans, W. "Budgeting for beginners: outstanding commitments." Nursing times vol. 81,50 (1985): 40-2.
Bryans W. Budgeting for beginners: outstanding commitments. Nurs Times. 1985 Dec 11-17;81(50):40-2. PMID: 3853195.
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Cooperative Catalysis: Calcium and Camphorsulfonic Acid Catalyzed Cycloisomerization of Diynols.

Chemistry (Weinheim an der Bergstrasse, Germany)

Rauser M, Schroeder S, Niggemann M.
PMID: 26403228
Chemistry. 2015 Nov 02;21(45):15929-33. doi: 10.1002/chem.201503293. Epub 2015 Sep 25.

The first transition metal-free cycloisomerization of easily accessible diynols is presented as a novel approach to bicyclic 2H-pyrans. As a one-step protocol, the reaction proceeds in a single reaction cascade by intertwining mechanistic fragments borrowed from transition metal-catalyzed Claisen...

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Rauser M, Schroeder S, Niggemann M. Cooperative Catalysis: Calcium and Camphorsulfonic Acid Catalyzed Cycloisomerization of Diynols. Chemistry. 2015;21(45):15929-33doi: 10.1002/chem.201503293.
Rauser, M., Schroeder, S., & Niggemann, M. (2015). Cooperative Catalysis: Calcium and Camphorsulfonic Acid Catalyzed Cycloisomerization of Diynols. Chemistry (Weinheim an der Bergstrasse, Germany), 21(45), 15929-33. https://doi.org/10.1002/chem.201503293
Rauser, Marian, et al. "Cooperative Catalysis: Calcium and Camphorsulfonic Acid Catalyzed Cycloisomerization of Diynols." Chemistry (Weinheim an der Bergstrasse, Germany) vol. 21,45 (2015): 15929-33. doi: https://doi.org/10.1002/chem.201503293
Rauser M, Schroeder S, Niggemann M. Cooperative Catalysis: Calcium and Camphorsulfonic Acid Catalyzed Cycloisomerization of Diynols. Chemistry. 2015 Nov 02;21(45):15929-33. doi: 10.1002/chem.201503293. Epub 2015 Sep 25. PMID: 26403228.
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Absentee patients: managing negative influences.

Perspectives in public health

Bryans W.
PMID: 27161273
Perspect Public Health. 2016 May;136(3):127-9. doi: 10.1177/1757913916638235.

No abstract available.

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Bryans W. Absentee patients: managing negative influences. Perspect Public Health. 2016;136(3):127-9doi: 10.1177/1757913916638235.
Bryans, W. (2016). Absentee patients: managing negative influences. Perspectives in public health, 136(3), 127-9. https://doi.org/10.1177/1757913916638235
Bryans, William. "Absentee patients: managing negative influences." Perspectives in public health vol. 136,3 (2016): 127-9. doi: https://doi.org/10.1177/1757913916638235
Bryans W. Absentee patients: managing negative influences. Perspect Public Health. 2016 May;136(3):127-9. doi: 10.1177/1757913916638235. PMID: 27161273.
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Bioequivalence and tolerability study of two brands of clopidogrel tablets, using inhibition of platelet aggregation and pharmacodynamic measures.

Current therapeutic research, clinical and experimental

Rao TR, Usha PR, Naidu MU, Gogtay JA, Meena M.
PMID: 24944416
Curr Ther Res Clin Exp. 2003 Nov;64(9):685-96. doi: 10.1016/j.curtheres.2003.09.014.

BACKGROUND: The role of platelets in acute cardiovascular atherothrombotic events has been well established and attention has focused on platelet inhibition therapy. Clopidogrel is a novel thienopyridine inhibitor of adenosine diphosphate-induced platelet activation. Recent studies have shown that in...

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Rao TR, Usha PR, Naidu MU, et al. Bioequivalence and tolerability study of two brands of clopidogrel tablets, using inhibition of platelet aggregation and pharmacodynamic measures. Curr Ther Res Clin Exp. 2003;64(9):685-96doi: 10.1016/j.curtheres.2003.09.014.
Rao, T. R., Usha, P. R., Naidu, M. U., Gogtay, J. A., & Meena, M. (2003). Bioequivalence and tolerability study of two brands of clopidogrel tablets, using inhibition of platelet aggregation and pharmacodynamic measures. Current therapeutic research, clinical and experimental, 64(9), 685-96. https://doi.org/10.1016/j.curtheres.2003.09.014
Rao, Takallapalli Ramesh Kumar, et al. "Bioequivalence and tolerability study of two brands of clopidogrel tablets, using inhibition of platelet aggregation and pharmacodynamic measures." Current therapeutic research, clinical and experimental vol. 64,9 (2003): 685-96. doi: https://doi.org/10.1016/j.curtheres.2003.09.014
Rao TR, Usha PR, Naidu MU, Gogtay JA, Meena M. Bioequivalence and tolerability study of two brands of clopidogrel tablets, using inhibition of platelet aggregation and pharmacodynamic measures. Curr Ther Res Clin Exp. 2003 Nov;64(9):685-96. doi: 10.1016/j.curtheres.2003.09.014. PMID: 24944416; PMCID: PMC4053054.
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Nickel-Catalyzed Reactions Directed toward the Formation of Heterocycles.

Accounts of chemical research

Kurahashi T, Matsubara S.
PMID: 25989256
Acc Chem Res. 2015 Jun 16;48(6):1703-16. doi: 10.1021/acs.accounts.5b00041. Epub 2015 May 19.

Heterocycles have garnered significant attention because they are important functional building blocks in various useful molecules, such as pharmaceuticals, agricultural chemicals, pesticides, and materials. Several studies have been conducted regarding the preparation of heterocyclic skeletons with an emphasis on...

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Kurahashi T, Matsubara S. Nickel-Catalyzed Reactions Directed toward the Formation of Heterocycles. Acc Chem Res. 2015;48(6):1703-16doi: 10.1021/acs.accounts.5b00041.
Kurahashi, T., & Matsubara, S. (2015). Nickel-Catalyzed Reactions Directed toward the Formation of Heterocycles. Accounts of chemical research, 48(6), 1703-16. https://doi.org/10.1021/acs.accounts.5b00041
Kurahashi, Takuya, and Matsubara, Seijiro. "Nickel-Catalyzed Reactions Directed toward the Formation of Heterocycles." Accounts of chemical research vol. 48,6 (2015): 1703-16. doi: https://doi.org/10.1021/acs.accounts.5b00041
Kurahashi T, Matsubara S. Nickel-Catalyzed Reactions Directed toward the Formation of Heterocycles. Acc Chem Res. 2015 Jun 16;48(6):1703-16. doi: 10.1021/acs.accounts.5b00041. Epub 2015 May 19. PMID: 25989256.
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EMAS position statement: Non-hormonal management of menopausal vasomotor symptoms.

Maturitas

Hunter MS.
PMID: 26351144
Maturitas. 2015 Dec;82(4):443. doi: 10.1016/j.maturitas.2015.08.012. Epub 2015 Sep 05.

No abstract available.

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Hunter MS. EMAS position statement: Non-hormonal management of menopausal vasomotor symptoms. Maturitas. 2015;82(4):443doi: 10.1016/j.maturitas.2015.08.012.
Hunter, M. S. (2015). EMAS position statement: Non-hormonal management of menopausal vasomotor symptoms. Maturitas, 82(4), 443. https://doi.org/10.1016/j.maturitas.2015.08.012
Hunter, Myra S. "EMAS position statement: Non-hormonal management of menopausal vasomotor symptoms." Maturitas vol. 82,4 (2015): 443. doi: https://doi.org/10.1016/j.maturitas.2015.08.012
Hunter MS. EMAS position statement: Non-hormonal management of menopausal vasomotor symptoms. Maturitas. 2015 Dec;82(4):443. doi: 10.1016/j.maturitas.2015.08.012. Epub 2015 Sep 05. PMID: 26351144.
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Changes in the Peripheral Blood Gene Expression Profile Induced by 3 Months of Valproate Treatment in Patients with Newly Diagnosed Epilepsy.

Frontiers in neurology

Rakitin A, Kõks S, Reimann E, Prans E, Haldre S.
PMID: 26379622
Front Neurol. 2015 Aug 31;6:188. doi: 10.3389/fneur.2015.00188. eCollection 2015.

Valproic acid (VPA) is a widely used antiepileptic drug with a broad range of effects and broad clinical efficacy. As a well-known histone deacetylase (HDAC) inhibitor, VPA regulates epigenetic programming by altering the expression of many genes. The aim...

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Rakitin A, Kõks S, Reimann E, et al. Changes in the Peripheral Blood Gene Expression Profile Induced by 3 Months of Valproate Treatment in Patients with Newly Diagnosed Epilepsy. Front Neurol. 2015;6:188doi: 10.3389/fneur.2015.00188.
Rakitin, A., Kõks, S., Reimann, E., Prans, E., & Haldre, S. (2015). Changes in the Peripheral Blood Gene Expression Profile Induced by 3 Months of Valproate Treatment in Patients with Newly Diagnosed Epilepsy. Frontiers in neurology, 6188. https://doi.org/10.3389/fneur.2015.00188
Rakitin, Aleksei, et al. "Changes in the Peripheral Blood Gene Expression Profile Induced by 3 Months of Valproate Treatment in Patients with Newly Diagnosed Epilepsy." Frontiers in neurology vol. 6 (2015): 188. doi: https://doi.org/10.3389/fneur.2015.00188
Rakitin A, Kõks S, Reimann E, Prans E, Haldre S. Changes in the Peripheral Blood Gene Expression Profile Induced by 3 Months of Valproate Treatment in Patients with Newly Diagnosed Epilepsy. Front Neurol. 2015 Aug 31;6:188. doi: 10.3389/fneur.2015.00188. eCollection 2015. PMID: 26379622; PMCID: PMC4553897.
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The stereoselective formation of highly substituted CF3-dihydropyrans as versatile building blocks.

Chemical communications (Cambridge, England)

Donslund BS, Monleón A, Larsen J, Ibsen L, Jørgensen KA.
PMID: 26225818
Chem Commun (Camb). 2015 Sep 14;51(71):13666-9. doi: 10.1039/c5cc04874e.

The highly enantioselective dienamine-mediated formation of 5-bromo-6-(trifluoromethyl)-3,4-dihydro-2H-pyrans from α,β-unsaturated aldehydes and α-bromo-(trifluoromethyl)-enones employing a C2-symmetric aminocatalyst is described. The products are demonstrated to be applicable in coupling reactions directly onto the ring, thereby granting access to a broad scope...

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Donslund BS, Monleón A, Larsen J, et al. The stereoselective formation of highly substituted CF3-dihydropyrans as versatile building blocks. Chem Commun (Camb). 2015;51(71):13666-9doi: 10.1039/c5cc04874e.
Donslund, B. S., Monleón, A., Larsen, J., Ibsen, L., & Jørgensen, K. A. (2015). The stereoselective formation of highly substituted CF3-dihydropyrans as versatile building blocks. Chemical communications (Cambridge, England), 51(71), 13666-9. https://doi.org/10.1039/c5cc04874e
Donslund, Bjarke S, et al. "The stereoselective formation of highly substituted CF3-dihydropyrans as versatile building blocks." Chemical communications (Cambridge, England) vol. 51,71 (2015): 13666-9. doi: https://doi.org/10.1039/c5cc04874e
Donslund BS, Monleón A, Larsen J, Ibsen L, Jørgensen KA. The stereoselective formation of highly substituted CF3-dihydropyrans as versatile building blocks. Chem Commun (Camb). 2015 Sep 14;51(71):13666-9. doi: 10.1039/c5cc04874e. PMID: 26225818.
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Ceria-Vanadia/Silica-Catalyzed Cascade for C-C and C-O Bond Activation: Green One-Pot Synthesis of 2-Amino-3-cyano-4H-pyrans.

ChemistryOpen

Maddila SN, Maddila S, van Zyl WE, Jonnalagadda SB.
PMID: 27308209
ChemistryOpen. 2015 Aug 19;5(1):38-42. doi: 10.1002/open.201500159. eCollection 2016 Feb.

We designed a ceria-vanadia/silica (Ce-V/SiO2) heterogeneous catalyst and used it for the green and efficient synthesis of 2-amino-3-cyano-4H-pyran derivatives. The green reaction was a multicomponent one-pot condensation of 5,5-dimethylcyclohexane-1,3-dione, aromatic aldehyde, and malononitrile in an eco-compatible solvent (ethanol). The...

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Maddila SN, Maddila S, van Zyl WE, et al. Ceria-Vanadia/Silica-Catalyzed Cascade for C-C and C-O Bond Activation: Green One-Pot Synthesis of 2-Amino-3-cyano-4H-pyrans. ChemistryOpen. 2015;5(1):38-42doi: 10.1002/open.201500159.
Maddila, S. N., Maddila, S., van Zyl, W. E., & Jonnalagadda, S. B. (2016). Ceria-Vanadia/Silica-Catalyzed Cascade for C-C and C-O Bond Activation: Green One-Pot Synthesis of 2-Amino-3-cyano-4H-pyrans. ChemistryOpen, 5(1), 38-42. https://doi.org/10.1002/open.201500159
Maddila, Surya Narayana, et al. "Ceria-Vanadia/Silica-Catalyzed Cascade for C-C and C-O Bond Activation: Green One-Pot Synthesis of 2-Amino-3-cyano-4H-pyrans." ChemistryOpen vol. 5,1 (2016): 38-42. doi: https://doi.org/10.1002/open.201500159
Maddila SN, Maddila S, van Zyl WE, Jonnalagadda SB. Ceria-Vanadia/Silica-Catalyzed Cascade for C-C and C-O Bond Activation: Green One-Pot Synthesis of 2-Amino-3-cyano-4H-pyrans. ChemistryOpen. 2015 Aug 19;5(1):38-42. doi: 10.1002/open.201500159. eCollection 2016 Feb. PMID: 27308209; PMCID: PMC4906492.
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Quality of Labor Epidural Analgesia and Maternal Outcome With Levobupivacaine and Ropivacaine: A Double-Blinded Randomized Trial.

Anesthesia, essays and researches

Kumar TS, Rani P, Hemanth Kumar VR, Samal S, Parthasarathy S, Ravishankar M.
PMID: 28298752
Anesth Essays Res. 2017 Jan-Mar;11(1):28-33. doi: 10.4103/0259-1162.194573.

BACKGROUND: Quality of labor analgesia plays a vital role in the maternal outcome. Very few literature are available analyzing the quality of epidural labor analgesia.AIM: The aim of this study was to compare the effectiveness of 0.1% levobupivacaine and...

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Kumar TS, Rani P, Hemanth Kumar VR, et al. Quality of Labor Epidural Analgesia and Maternal Outcome With Levobupivacaine and Ropivacaine: A Double-Blinded Randomized Trial. Anesth Essays Res. 2017;11(1):28-33doi: 10.4103/0259-1162.194573.
Kumar, T. S., Rani, P., Hemanth Kumar, V. R., Samal, S., Parthasarathy, S., & Ravishankar, M. (2017). Quality of Labor Epidural Analgesia and Maternal Outcome With Levobupivacaine and Ropivacaine: A Double-Blinded Randomized Trial. Anesthesia, essays and researches, 11(1), 28-33. https://doi.org/10.4103/0259-1162.194573
Kumar, T Senthil, et al. "Quality of Labor Epidural Analgesia and Maternal Outcome With Levobupivacaine and Ropivacaine: A Double-Blinded Randomized Trial." Anesthesia, essays and researches vol. 11,1 (2017): 28-33. doi: https://doi.org/10.4103/0259-1162.194573
Kumar TS, Rani P, Hemanth Kumar VR, Samal S, Parthasarathy S, Ravishankar M. Quality of Labor Epidural Analgesia and Maternal Outcome With Levobupivacaine and Ropivacaine: A Double-Blinded Randomized Trial. Anesth Essays Res. 2017 Jan-Mar;11(1):28-33. doi: 10.4103/0259-1162.194573. PMID: 28298752; PMCID: PMC5341640.
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Addition-Rearrangement of Aryl- and Alkoxysulfonyl Isocyanates with 5-Methyl-Substituted 3,4-Dihydro-2-methoxy-2H-pyrans. Selective Synthesis of Functionalized 2-Piperidones(1).

The Journal of organic chemistry

Jao E, Slifer PB, Lalancette R, Hall SS.
PMID: 11667125
J Org Chem. 1996 Apr 19;61(8):2865-2870. doi: 10.1021/jo951868o.

3,4-Dihydro-2-methoxy-5-methyl-2H-pyran and 3,4-dihydro-2-methoxy-5,6-dimethyl-2H-pyran undergo addition-rearrangement reactions with arylsulfonyl isocyanates to generate the corresponding 3-formyl- and 3-acetyl-6-methoxy-3-methyl-1-(arylsulfonyl)-2-piperidones. For example, 3,4-dihydro-2-methoxy-5-methyl-2H-pyran and phenylsulfonyl isocyanate afforded 3-formyl-6-methoxy-3-methyl-1-(phenylsulfonyl)-2-piperidone as a separable trans/cis mixture in high yield. The more reactive phenoxysulfonyl and alkoxysulfonyl isocyanates...

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Jao E, Slifer PB, Lalancette R, et al. Addition-Rearrangement of Aryl- and Alkoxysulfonyl Isocyanates with 5-Methyl-Substituted 3,4-Dihydro-2-methoxy-2H-pyrans. Selective Synthesis of Functionalized 2-Piperidones(1). J Org Chem. 1996;61(8):2865-2870doi: 10.1021/jo951868o.
Jao, E., Slifer, P. B., Lalancette, R., & Hall, S. S. (1996). Addition-Rearrangement of Aryl- and Alkoxysulfonyl Isocyanates with 5-Methyl-Substituted 3,4-Dihydro-2-methoxy-2H-pyrans. Selective Synthesis of Functionalized 2-Piperidones(1). The Journal of organic chemistry, 61(8), 2865-2870. https://doi.org/10.1021/jo951868o
Jao, Edwin, et al. "Addition-Rearrangement of Aryl- and Alkoxysulfonyl Isocyanates with 5-Methyl-Substituted 3,4-Dihydro-2-methoxy-2H-pyrans. Selective Synthesis of Functionalized 2-Piperidones(1)." The Journal of organic chemistry vol. 61,8 (1996): 2865-2870. doi: https://doi.org/10.1021/jo951868o
Jao E, Slifer PB, Lalancette R, Hall SS. Addition-Rearrangement of Aryl- and Alkoxysulfonyl Isocyanates with 5-Methyl-Substituted 3,4-Dihydro-2-methoxy-2H-pyrans. Selective Synthesis of Functionalized 2-Piperidones(1). J Org Chem. 1996 Apr 19;61(8):2865-2870. doi: 10.1021/jo951868o. PMID: 11667125.
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Showing 1 to 12 of 299 entries