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How long lasting are the effects of training on interaction skills? Teachers' sample

classroom interventions

Ketonen E, Lonka K, Talvio M.
GSID: Ydg0q1BX5TAJ
M Talvio, E Ketonen, K Lonka - Proceedings of 2014 international …, 2014 - academia.edu

Social interaction skills are emphasized as key tools in modern learning psychology. Research, however, is scarce how teachers study and learn these skills. The aim of the …

[Some answers to the nursing shortage].

Zeitschrift fur Krankenpflege. Revue suisse des infirmieres

Jones K.
PMID: 5195267
Z Krankenpfl. 1969 Sep;62(9):371-2.

No abstract available.

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Jones K. Quelques réponses au manque de personnel infirmier. [Some answers to the nursing shortage]. Z Krankenpfl. 1969;62(9):371-2
Jones, K. (1969). Quelques réponses au manque de personnel infirmier. [Some answers to the nursing shortage]. Zeitschrift fur Krankenpflege. Revue suisse des infirmieres, 62(9), 371-2.
Jones, K. "Quelques réponses au manque de personnel infirmier." [Some answers to the nursing shortage]. Zeitschrift fur Krankenpflege. Revue suisse des infirmieres vol. 62,9 (1969): 371-2.
Jones K. Quelques réponses au manque de personnel infirmier. [Some answers to the nursing shortage]. Z Krankenpfl. 1969 Sep;62(9):371-2. French. PMID: 5195267.
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Nucleopalladation triggering the oxidative Heck reaction: a general strategy to diverse β-indole ketones.

Organic letters

Wang Q, Huang L, Wu X, Jiang H.
PMID: 24237319
Org Lett. 2013 Dec 06;15(23):5940-3. doi: 10.1021/ol4027683. Epub 2013 Nov 15.

A simple and efficient palladium-catalyzed oxidative coupling between 2-alkynyl anilines and allylic alcohols is described by using cheap and green dioxygen as the oxidant. These cross-couplings have a large functional group tolerance and are of higher reactivity toward electron...

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Wang Q, Huang L, Wu X, et al. Nucleopalladation triggering the oxidative Heck reaction: a general strategy to diverse β-indole ketones. Org Lett. 2013;15(23):5940-3doi: 10.1021/ol4027683.
Wang, Q., Huang, L., Wu, X., & Jiang, H. (2013). Nucleopalladation triggering the oxidative Heck reaction: a general strategy to diverse β-indole ketones. Organic letters, 15(23), 5940-3. https://doi.org/10.1021/ol4027683
Wang, Qian, et al. "Nucleopalladation triggering the oxidative Heck reaction: a general strategy to diverse β-indole ketones." Organic letters vol. 15,23 (2013): 5940-3. doi: https://doi.org/10.1021/ol4027683
Wang Q, Huang L, Wu X, Jiang H. Nucleopalladation triggering the oxidative Heck reaction: a general strategy to diverse β-indole ketones. Org Lett. 2013 Dec 06;15(23):5940-3. doi: 10.1021/ol4027683. Epub 2013 Nov 15. PMID: 24237319.
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Metal-free nitroxyl radical-mediated β-C(sp.

Chemical communications (Cambridge, England)

Qian P, Deng Y, Mei H, Han J, Pan Y.
PMID: 28229143
Chem Commun (Camb). 2017 Mar 07;53(20):2958-2961. doi: 10.1039/c7cc00145b.

The first metal-free nitroxyl-radical-mediated β-amination of saturated ketones by using heteroaryl halides as amide precursors has been developed. This reaction proceeds through a cascade α-aminoxylation/Cope-like elimination/aza-Michael addition sequence to afford β-amino ketone derivatives with excellent yields. TEMPO plays multiple...

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Qian P, Deng Y, Mei H, et al. Metal-free nitroxyl radical-mediated β-C(sp. Chem Commun (Camb). 2017;53(20):2958-2961doi: 10.1039/c7cc00145b.
Qian, P., Deng, Y., Mei, H., Han, J., & Pan, Y. (2017). Metal-free nitroxyl radical-mediated β-C(sp. Chemical communications (Cambridge, England), 53(20), 2958-2961. https://doi.org/10.1039/c7cc00145b
Qian, Ping, et al. "Metal-free nitroxyl radical-mediated β-C(sp." Chemical communications (Cambridge, England) vol. 53,20 (2017): 2958-2961. doi: https://doi.org/10.1039/c7cc00145b
Qian P, Deng Y, Mei H, Han J, Pan Y. Metal-free nitroxyl radical-mediated β-C(sp. Chem Commun (Camb). 2017 Mar 07;53(20):2958-2961. doi: 10.1039/c7cc00145b. PMID: 28229143.
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Efficient hydroxymethylation reactions of iodoarenes using CO and 1,3-dimethylimidazol-2-ylidene borane.

Organic letters

Kawamoto T, Okada T, Curran DP, Ryu I.
PMID: 23590524
Org Lett. 2013 May 03;15(9):2144-7. doi: 10.1021/ol4006294. Epub 2013 Apr 16.

A hydroxymethylation reaction of a variety of iodoarenes proceeded effectively in the presence of CO, NHC-borane, diMeImd-BH3 (2) as a radical mediator, and a catalytic amount of AIBN. The reaction took place chemoselectively at the aryl-iodine bond but not...

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Kawamoto T, Okada T, Curran DP, et al. Efficient hydroxymethylation reactions of iodoarenes using CO and 1,3-dimethylimidazol-2-ylidene borane. Org Lett. 2013;15(9):2144-7doi: 10.1021/ol4006294.
Kawamoto, T., Okada, T., Curran, D. P., & Ryu, I. (2013). Efficient hydroxymethylation reactions of iodoarenes using CO and 1,3-dimethylimidazol-2-ylidene borane. Organic letters, 15(9), 2144-7. https://doi.org/10.1021/ol4006294
Kawamoto, Takuji, et al. "Efficient hydroxymethylation reactions of iodoarenes using CO and 1,3-dimethylimidazol-2-ylidene borane." Organic letters vol. 15,9 (2013): 2144-7. doi: https://doi.org/10.1021/ol4006294
Kawamoto T, Okada T, Curran DP, Ryu I. Efficient hydroxymethylation reactions of iodoarenes using CO and 1,3-dimethylimidazol-2-ylidene borane. Org Lett. 2013 May 03;15(9):2144-7. doi: 10.1021/ol4006294. Epub 2013 Apr 16. PMID: 23590524.
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Synthesis of novel N-cyclopentenyl-lactams using the Aubé reaction.

Beilstein journal of organic chemistry

Shinde MV, Ople RS, Sangtani E, Gonnade R, Reddy DS.
PMID: 26199661
Beilstein J Org Chem. 2015 Jun 23;11:1060-7. doi: 10.3762/bjoc.11.119. eCollection 2015.

A novel and convenient method utilizing the Aubé reaction to access a new class of compounds that are similar to carbocyclic nucleosides is reported. The azido alcohol derived from Vince lactam undergoes the Aubé reaction with various cyclic ketones...

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Shinde MV, Ople RS, Sangtani E, et al. Synthesis of novel N-cyclopentenyl-lactams using the Aubé reaction. Beilstein J Org Chem. 2015;11:1060-7doi: 10.3762/bjoc.11.119.
Shinde, M. V., Ople, R. S., Sangtani, E., Gonnade, R., & Reddy, D. S. (2015). Synthesis of novel N-cyclopentenyl-lactams using the Aubé reaction. Beilstein journal of organic chemistry, 111060-7. https://doi.org/10.3762/bjoc.11.119
Shinde, Madhuri V, et al. "Synthesis of novel N-cyclopentenyl-lactams using the Aubé reaction." Beilstein journal of organic chemistry vol. 11 (2015): 1060-7. doi: https://doi.org/10.3762/bjoc.11.119
Shinde MV, Ople RS, Sangtani E, Gonnade R, Reddy DS. Synthesis of novel N-cyclopentenyl-lactams using the Aubé reaction. Beilstein J Org Chem. 2015 Jun 23;11:1060-7. doi: 10.3762/bjoc.11.119. eCollection 2015. PMID: 26199661; PMCID: PMC4505090.
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Chemical compositions of the volatile extracts from seeds of Dendranthema nankingense and Borago officinalis.

Journal of food and drug analysis

Wu S, Xu T, Huang D.
PMID: 28911380
J Food Drug Anal. 2015 Jun;23(2):253-259. doi: 10.1016/j.jfda.2014.10.006. Epub 2014 Dec 03.

Volatile extracts from the seeds of Dendranthema nankingense Hand.-Mazz. and Borago officinalis L. were prepared using simultaneous distillation and extraction, and analyzed with gas chromatography-mass spectrometry on two capillary gas chromatography columns of different polarity. Ninety-five volatile compounds were...

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Wu S, Xu T, Huang D. Chemical compositions of the volatile extracts from seeds of Dendranthema nankingense and Borago officinalis. J Food Drug Anal. 2014;23(2):253-259doi: 10.1016/j.jfda.2014.10.006.
Wu, S., Xu, T., & Huang, D. (2015). Chemical compositions of the volatile extracts from seeds of Dendranthema nankingense and Borago officinalis. Journal of food and drug analysis, 23(2), 253-259. https://doi.org/10.1016/j.jfda.2014.10.006
Wu, Shimin, et al. "Chemical compositions of the volatile extracts from seeds of Dendranthema nankingense and Borago officinalis." Journal of food and drug analysis vol. 23,2 (2015): 253-259. doi: https://doi.org/10.1016/j.jfda.2014.10.006
Wu S, Xu T, Huang D. Chemical compositions of the volatile extracts from seeds of Dendranthema nankingense and Borago officinalis. J Food Drug Anal. 2015 Jun;23(2):253-259. doi: 10.1016/j.jfda.2014.10.006. Epub 2014 Dec 03. PMID: 28911380.
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Highly Enantioselective Construction of Fluoroalkylated Quaternary Stereocenters via Organocatalytic Dehydrated Mannich Reaction of Unprotected Hemiaminals with Ketones.

Organic letters

Zhang S, Li L, Hu Y, Li Y, Yang Y, Zha Z, Wang Z.
PMID: 26414655
Org Lett. 2015 Oct 16;17(20):5036-9. doi: 10.1021/acs.orglett.5b02514. Epub 2015 Sep 28.

A general organocatalytic asymmetric dehydrated Mannich reaction of fluoroalkyl hemiaminals with ketones is reported. In this Mannich reaction, previously less explored aryl ketones showed great reactivity. By virtue of this efficient method, a wide range of biologically active β-amino...

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Zhang S, Li L, Hu Y, et al. Highly Enantioselective Construction of Fluoroalkylated Quaternary Stereocenters via Organocatalytic Dehydrated Mannich Reaction of Unprotected Hemiaminals with Ketones. Org Lett. 2015;17(20):5036-9doi: 10.1021/acs.orglett.5b02514.
Zhang, S., Li, L., Hu, Y., Li, Y., Yang, Y., Zha, Z., & Wang, Z. (2015). Highly Enantioselective Construction of Fluoroalkylated Quaternary Stereocenters via Organocatalytic Dehydrated Mannich Reaction of Unprotected Hemiaminals with Ketones. Organic letters, 17(20), 5036-9. https://doi.org/10.1021/acs.orglett.5b02514
Zhang, Sheng, et al. "Highly Enantioselective Construction of Fluoroalkylated Quaternary Stereocenters via Organocatalytic Dehydrated Mannich Reaction of Unprotected Hemiaminals with Ketones." Organic letters vol. 17,20 (2015): 5036-9. doi: https://doi.org/10.1021/acs.orglett.5b02514
Zhang S, Li L, Hu Y, Li Y, Yang Y, Zha Z, Wang Z. Highly Enantioselective Construction of Fluoroalkylated Quaternary Stereocenters via Organocatalytic Dehydrated Mannich Reaction of Unprotected Hemiaminals with Ketones. Org Lett. 2015 Oct 16;17(20):5036-9. doi: 10.1021/acs.orglett.5b02514. Epub 2015 Sep 28. PMID: 26414655.
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Synthesis of Quinolines via a Metal-Catalyzed Dehydrogenative N-Heterocyclization.

Chemical record (New York, N.Y.)

Chelucci G, Porcheddu A.
PMID: 27524555
Chem Rec. 2017 Feb;17(2):200-216. doi: 10.1002/tcr.201600083. Epub 2016 Aug 15.

Efficient ruthenium-, rhodium-, palladium-, copper- and iridium-catalysed methodologies have been recently developed for the synthesis of quinolines by the reaction of 2-aminobenzyl alcohols with carbonyl compounds (aldehydes and ketones) or the related alcohols. The reaction is assumed to proceed...

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Chelucci G, Porcheddu A. Synthesis of Quinolines via a Metal-Catalyzed Dehydrogenative N-Heterocyclization. Chem Rec. 2016;17(2):200-216doi: 10.1002/tcr.201600083.
Chelucci, G., & Porcheddu, A. (2017). Synthesis of Quinolines via a Metal-Catalyzed Dehydrogenative N-Heterocyclization. Chemical record (New York, N.Y.), 17(2), 200-216. https://doi.org/10.1002/tcr.201600083
Chelucci, Giorgio, and Porcheddu, Andrea. "Synthesis of Quinolines via a Metal-Catalyzed Dehydrogenative N-Heterocyclization." Chemical record (New York, N.Y.) vol. 17,2 (2017): 200-216. doi: https://doi.org/10.1002/tcr.201600083
Chelucci G, Porcheddu A. Synthesis of Quinolines via a Metal-Catalyzed Dehydrogenative N-Heterocyclization. Chem Rec. 2017 Feb;17(2):200-216. doi: 10.1002/tcr.201600083. Epub 2016 Aug 15. PMID: 27524555.
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Organocatalytic Enantioselective Protonation for Photoreduction of Activated Ketones and Ketimines Induced by Visible Light.

Angewandte Chemie (International ed. in English)

Lin L, Bai X, Ye X, Zhao X, Tan CH, Jiang Z.
PMID: 28925022
Angew Chem Int Ed Engl. 2017 Oct 23;56(44):13842-13846. doi: 10.1002/anie.201707899. Epub 2017 Oct 04.

The first catalytic asymmetric photoreduction of 1,2-diketones and α-keto ketimines under visible light irradiation is reported. A transition-metal-free synergistic catalysis platform harnessing dicyanopyrazine-derived chromophore (DPZ) as the photoredox catalyst and a non-covalent chiral organocatalyst is effective for these transformations....

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Lin L, Bai X, Ye X, et al. Organocatalytic Enantioselective Protonation for Photoreduction of Activated Ketones and Ketimines Induced by Visible Light. Angew Chem Int Ed Engl. 2017;56(44):13842-13846doi: 10.1002/anie.201707899.
Lin, L., Bai, X., Ye, X., Zhao, X., Tan, C. H., & Jiang, Z. (2017). Organocatalytic Enantioselective Protonation for Photoreduction of Activated Ketones and Ketimines Induced by Visible Light. Angewandte Chemie (International ed. in English), 56(44), 13842-13846. https://doi.org/10.1002/anie.201707899
Lin, Lu, et al. "Organocatalytic Enantioselective Protonation for Photoreduction of Activated Ketones and Ketimines Induced by Visible Light." Angewandte Chemie (International ed. in English) vol. 56,44 (2017): 13842-13846. doi: https://doi.org/10.1002/anie.201707899
Lin L, Bai X, Ye X, Zhao X, Tan CH, Jiang Z. Organocatalytic Enantioselective Protonation for Photoreduction of Activated Ketones and Ketimines Induced by Visible Light. Angew Chem Int Ed Engl. 2017 Oct 23;56(44):13842-13846. doi: 10.1002/anie.201707899. Epub 2017 Oct 04. PMID: 28925022.
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Catalytic Asymmetric Electrochemical Oxidative Coupling of Tertiary Amines with Simple Ketones.

Organic letters

Fu N, Li L, Yang Q, Luo S.
PMID: 28394132
Org Lett. 2017 Apr 21;19(8):2122-2125. doi: 10.1021/acs.orglett.7b00746. Epub 2017 Apr 10.

Catalytic asymmetric electrochemical C-H functionalization of simple ketones has been developed. The transformation is realized by the combination of electrochemical oxidation and chiral primary amine catalysis. This metal- and oxidant-free method furnishes diverse C1-alkylated tetrahydroisoquinolines in high yields and...

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Fu N, Li L, Yang Q, et al. Catalytic Asymmetric Electrochemical Oxidative Coupling of Tertiary Amines with Simple Ketones. Org Lett. 2017;19(8):2122-2125doi: 10.1021/acs.orglett.7b00746.
Fu, N., Li, L., Yang, Q., & Luo, S. (2017). Catalytic Asymmetric Electrochemical Oxidative Coupling of Tertiary Amines with Simple Ketones. Organic letters, 19(8), 2122-2125. https://doi.org/10.1021/acs.orglett.7b00746
Fu, Niankai, et al. "Catalytic Asymmetric Electrochemical Oxidative Coupling of Tertiary Amines with Simple Ketones." Organic letters vol. 19,8 (2017): 2122-2125. doi: https://doi.org/10.1021/acs.orglett.7b00746
Fu N, Li L, Yang Q, Luo S. Catalytic Asymmetric Electrochemical Oxidative Coupling of Tertiary Amines with Simple Ketones. Org Lett. 2017 Apr 21;19(8):2122-2125. doi: 10.1021/acs.orglett.7b00746. Epub 2017 Apr 10. PMID: 28394132.
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Gold(I)-Catalyzed Cascade Hydroarylation/Cycloaromatization to Indolizines via Pyridine Ring Construction.

The Journal of organic chemistry

Li X, Xie X, Liu Y.
PMID: 27035285
J Org Chem. 2016 May 06;81(9):3688-99. doi: 10.1021/acs.joc.6b00346. Epub 2016 Apr 08.

An efficient and atom-economic method for the synthesis of multisubstituted indolizines via gold-catalyzed cascade hydroarylation/cycloaromatization reaction of α-(N-pyrrolyl)ketones with alkynes is described. The reaction is realized through the construction of the pyridine ring of indolizines, which allows the regioselective...

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Li X, Xie X, Liu Y. Gold(I)-Catalyzed Cascade Hydroarylation/Cycloaromatization to Indolizines via Pyridine Ring Construction. J Org Chem. 2016;81(9):3688-99doi: 10.1021/acs.joc.6b00346.
Li, X., Xie, X., & Liu, Y. (2016). Gold(I)-Catalyzed Cascade Hydroarylation/Cycloaromatization to Indolizines via Pyridine Ring Construction. The Journal of organic chemistry, 81(9), 3688-99. https://doi.org/10.1021/acs.joc.6b00346
Li, Xiangdong, et al. "Gold(I)-Catalyzed Cascade Hydroarylation/Cycloaromatization to Indolizines via Pyridine Ring Construction." The Journal of organic chemistry vol. 81,9 (2016): 3688-99. doi: https://doi.org/10.1021/acs.joc.6b00346
Li X, Xie X, Liu Y. Gold(I)-Catalyzed Cascade Hydroarylation/Cycloaromatization to Indolizines via Pyridine Ring Construction. J Org Chem. 2016 May 06;81(9):3688-99. doi: 10.1021/acs.joc.6b00346. Epub 2016 Apr 08. PMID: 27035285.
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Showing 1 to 12 of 6641 entries