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An econometric analysis of the major choice of first-generation college students

first generation college student

Trejo S.
GSID: HHJD5ZizD4IJ
S Trejo - The Developing Economist, 2016 - inquiriesjournal.com

… that first-generation college students select that major relative to otherwise identical non-first generation students. … , the likelihood that first-generation college students select that major …

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Trejo, S. (2016). An econometric analysis of the major choice of first-generation college students. The Developing Economist, 3(1).
Trejo, Sam. "An econometric analysis of the major choice of first-generation college students." The Developing Economist 3.1 (2016).
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Copper-catalyzed hydroallylation of allenes employing hydrosilanes and allyl chlorides.

Chemical communications (Cambridge, England)

Fujihara T, Yokota K, Terao J, Tsuji Y.
PMID: 28513657
Chem Commun (Camb). 2017 Jul 11;53(56):7898-7900. doi: 10.1039/c7cc02816d.

The hydroallylation of allenes was developed by employing a hydrosilane and allyl chlorides in the presence of a copper catalyst. The reaction provided (E)-1,5-dienes mainly in good to high yields.

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Fujihara T, Yokota K, Terao J, et al. Copper-catalyzed hydroallylation of allenes employing hydrosilanes and allyl chlorides. Chem Commun (Camb). 2017;53(56):7898-7900doi: 10.1039/c7cc02816d.
Fujihara, T., Yokota, K., Terao, J., & Tsuji, Y. (2017). Copper-catalyzed hydroallylation of allenes employing hydrosilanes and allyl chlorides. Chemical communications (Cambridge, England), 53(56), 7898-7900. https://doi.org/10.1039/c7cc02816d
Fujihara, Tetsuaki, et al. "Copper-catalyzed hydroallylation of allenes employing hydrosilanes and allyl chlorides." Chemical communications (Cambridge, England) vol. 53,56 (2017): 7898-7900. doi: https://doi.org/10.1039/c7cc02816d
Fujihara T, Yokota K, Terao J, Tsuji Y. Copper-catalyzed hydroallylation of allenes employing hydrosilanes and allyl chlorides. Chem Commun (Camb). 2017 Jul 11;53(56):7898-7900. doi: 10.1039/c7cc02816d. PMID: 28513657.
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Copper-catalyzed C-C bond-forming transformation of CO2 to alcohol oxidation level: selective synthesis of homoallylic alcohols from allenes, CO2, and hydrosilanes.

Chemical communications (Cambridge, England)

Tani Y, Kuga K, Fujihara T, Terao J, Tsuji Y.
PMID: 26179158
Chem Commun (Camb). 2015 Aug 21;51(65):13020-3. doi: 10.1039/c5cc03932k.

A highly selective carbon-carbon bond-forming transformation of carbon dioxide (CO2) to alcohol oxidation level has been disclosed. By employing a copper/bisphosphine catalyst system and hydrosilanes as mild and easy-to-handle reducing agents, various allenes can be reacted with CO2 to...

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Tani Y, Kuga K, Fujihara T, et al. Copper-catalyzed C-C bond-forming transformation of CO2 to alcohol oxidation level: selective synthesis of homoallylic alcohols from allenes, CO2, and hydrosilanes. Chem Commun (Camb). 2015;51(65):13020-3doi: 10.1039/c5cc03932k.
Tani, Y., Kuga, K., Fujihara, T., Terao, J., & Tsuji, Y. (2015). Copper-catalyzed C-C bond-forming transformation of CO2 to alcohol oxidation level: selective synthesis of homoallylic alcohols from allenes, CO2, and hydrosilanes. Chemical communications (Cambridge, England), 51(65), 13020-3. https://doi.org/10.1039/c5cc03932k
Tani, Yosuke, et al. "Copper-catalyzed C-C bond-forming transformation of CO2 to alcohol oxidation level: selective synthesis of homoallylic alcohols from allenes, CO2, and hydrosilanes." Chemical communications (Cambridge, England) vol. 51,65 (2015): 13020-3. doi: https://doi.org/10.1039/c5cc03932k
Tani Y, Kuga K, Fujihara T, Terao J, Tsuji Y. Copper-catalyzed C-C bond-forming transformation of CO2 to alcohol oxidation level: selective synthesis of homoallylic alcohols from allenes, CO2, and hydrosilanes. Chem Commun (Camb). 2015 Aug 21;51(65):13020-3. doi: 10.1039/c5cc03932k. PMID: 26179158.
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Hetero Face-to-Face Porphyrin Array with Cooperative Effects of Coordination and Host-Guest Complexation.

Chemistry, an Asian journal

Chiba Y, Liu M, Tachibana Y, Fujihara T, Tsuji Y, Terao J.
PMID: 28544526
Chem Asian J. 2017 Aug 04;12(15):1900-1904. doi: 10.1002/asia.201700738. Epub 2017 Jul 03.

We successfully synthesized a hetero face-to-face porphyrin array composed of ZnTPP and RuTPP(DABCO)

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Chiba Y, Liu M, Tachibana Y, et al. Hetero Face-to-Face Porphyrin Array with Cooperative Effects of Coordination and Host-Guest Complexation. Chem Asian J. 2017;12(15):1900-1904doi: 10.1002/asia.201700738.
Chiba, Y., Liu, M., Tachibana, Y., Fujihara, T., Tsuji, Y., & Terao, J. (2017). Hetero Face-to-Face Porphyrin Array with Cooperative Effects of Coordination and Host-Guest Complexation. Chemistry, an Asian journal, 12(15), 1900-1904. https://doi.org/10.1002/asia.201700738
Chiba, Yusuke, et al. "Hetero Face-to-Face Porphyrin Array with Cooperative Effects of Coordination and Host-Guest Complexation." Chemistry, an Asian journal vol. 12,15 (2017): 1900-1904. doi: https://doi.org/10.1002/asia.201700738
Chiba Y, Liu M, Tachibana Y, Fujihara T, Tsuji Y, Terao J. Hetero Face-to-Face Porphyrin Array with Cooperative Effects of Coordination and Host-Guest Complexation. Chem Asian J. 2017 Aug 04;12(15):1900-1904. doi: 10.1002/asia.201700738. Epub 2017 Jul 03. PMID: 28544526.
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Cobalt-catalyzed carboxylation of propargyl acetates with carbon dioxide.

Chemical communications (Cambridge, England)

Nogi K, Fujihara T, Terao J, Tsuji Y.
PMID: 24966094
Chem Commun (Camb). 2014 Nov 07;50(86):13052-5. doi: 10.1039/c4cc03644a.

The cobalt-catalyzed carboxylation of propargyl acetates with CO2 (1 atm) is described. The reaction proceeds at room temperature in the presence of Mn powder as a reducing reagent. Various propargyl acetates are converted to the corresponding carboxylic acids in...

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Nogi K, Fujihara T, Terao J, et al. Cobalt-catalyzed carboxylation of propargyl acetates with carbon dioxide. Chem Commun (Camb). 2014;50(86):13052-5doi: 10.1039/c4cc03644a.
Nogi, K., Fujihara, T., Terao, J., & Tsuji, Y. (2014). Cobalt-catalyzed carboxylation of propargyl acetates with carbon dioxide. Chemical communications (Cambridge, England), 50(86), 13052-5. https://doi.org/10.1039/c4cc03644a
Nogi, Keisuke, et al. "Cobalt-catalyzed carboxylation of propargyl acetates with carbon dioxide." Chemical communications (Cambridge, England) vol. 50,86 (2014): 13052-5. doi: https://doi.org/10.1039/c4cc03644a
Nogi K, Fujihara T, Terao J, Tsuji Y. Cobalt-catalyzed carboxylation of propargyl acetates with carbon dioxide. Chem Commun (Camb). 2014 Nov 07;50(86):13052-5. doi: 10.1039/c4cc03644a. PMID: 24966094.
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Palladium-catalyzed formal arylacylation of allenes employing acid chlorides and arylboronic acids.

Chemical communications (Cambridge, England)

Tatsumi K, Fujihara T, Terao J, Tsuji Y.
PMID: 24871994
Chem Commun (Camb). 2014 Aug 11;50(62):8476-9. doi: 10.1039/c4cc03173c.

Palladium-catalyzed formal arylacylation of allenes using acid chlorides and arylboronic acids has been achieved. The reaction afforded the corresponding α,β-unsaturated ketones regio- and stereoselectively.

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Tatsumi K, Fujihara T, Terao J, et al. Palladium-catalyzed formal arylacylation of allenes employing acid chlorides and arylboronic acids. Chem Commun (Camb). 2014;50(62):8476-9doi: 10.1039/c4cc03173c.
Tatsumi, K., Fujihara, T., Terao, J., & Tsuji, Y. (2014). Palladium-catalyzed formal arylacylation of allenes employing acid chlorides and arylboronic acids. Chemical communications (Cambridge, England), 50(62), 8476-9. https://doi.org/10.1039/c4cc03173c
Tatsumi, Kenta, et al. "Palladium-catalyzed formal arylacylation of allenes employing acid chlorides and arylboronic acids." Chemical communications (Cambridge, England) vol. 50,62 (2014): 8476-9. doi: https://doi.org/10.1039/c4cc03173c
Tatsumi K, Fujihara T, Terao J, Tsuji Y. Palladium-catalyzed formal arylacylation of allenes employing acid chlorides and arylboronic acids. Chem Commun (Camb). 2014 Aug 11;50(62):8476-9. doi: 10.1039/c4cc03173c. PMID: 24871994.
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Synthesis of an organic-soluble π-conjugated [3]rotaxane via rotation of glucopyranose units in permethylated β-cyclodextrin.

Beilstein journal of organic chemistry

Terao J, Konoshima Y, Matono A, Masai H, Fujihara T, Tsuji Y.
PMID: 25550746
Beilstein J Org Chem. 2014 Nov 28;10:2800-8. doi: 10.3762/bjoc.10.297. eCollection 2014.

We synthesized symmetrically insulated oligo(para-phenylene) and oligothiophene with a pseudo-linked [3]rotaxane structure by full rotation of glucopyranose units via a flipping (tumbling) mechanism in the π-conjugated guest having two permethylated β-cyclodextrin units at both ends. We also succeeded in...

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Terao J, Konoshima Y, Matono A, et al. Synthesis of an organic-soluble π-conjugated [3]rotaxane via rotation of glucopyranose units in permethylated β-cyclodextrin. Beilstein J Org Chem. 2014;10:2800-8doi: 10.3762/bjoc.10.297.
Terao, J., Konoshima, Y., Matono, A., Masai, H., Fujihara, T., & Tsuji, Y. (2014). Synthesis of an organic-soluble π-conjugated [3]rotaxane via rotation of glucopyranose units in permethylated β-cyclodextrin. Beilstein journal of organic chemistry, 102800-8. https://doi.org/10.3762/bjoc.10.297
Terao, Jun, et al. "Synthesis of an organic-soluble π-conjugated [3]rotaxane via rotation of glucopyranose units in permethylated β-cyclodextrin." Beilstein journal of organic chemistry vol. 10 (2014): 2800-8. doi: https://doi.org/10.3762/bjoc.10.297
Terao J, Konoshima Y, Matono A, Masai H, Fujihara T, Tsuji Y. Synthesis of an organic-soluble π-conjugated [3]rotaxane via rotation of glucopyranose units in permethylated β-cyclodextrin. Beilstein J Org Chem. 2014 Nov 28;10:2800-8. doi: 10.3762/bjoc.10.297. eCollection 2014. PMID: 25550746; PMCID: PMC4273295.
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Form birefringence in Kerr media: analytical formulation and rigorous theory.

Optics letters

Bej S, Tervo J, Svirko YP, Turunen J.
PMID: 26076294
Opt Lett. 2015 Jun 15;40(12):2913-6. doi: 10.1364/OL.40.002913.

Employing the first-order effective medium theory, we develop an analytical model that governs light propagation inside a form birefringent medium with isotropic dielectric Kerr nonlinear material. This analytical model is found to be in excellent agreement with the recently...

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Bej S, Tervo J, Svirko YP, et al. Form birefringence in Kerr media: analytical formulation and rigorous theory. Opt Lett. 2015;40(12):2913-6doi: 10.1364/OL.40.002913.
Bej, S., Tervo, J., Svirko, Y. P., & Turunen, J. (2015). Form birefringence in Kerr media: analytical formulation and rigorous theory. Optics letters, 40(12), 2913-6. https://doi.org/10.1364/OL.40.002913
Bej, Subhajit, et al. "Form birefringence in Kerr media: analytical formulation and rigorous theory." Optics letters vol. 40,12 (2015): 2913-6. doi: https://doi.org/10.1364/OL.40.002913
Bej S, Tervo J, Svirko YP, Turunen J. Form birefringence in Kerr media: analytical formulation and rigorous theory. Opt Lett. 2015 Jun 15;40(12):2913-6. doi: 10.1364/OL.40.002913. PMID: 26076294.
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A Typical Metal-Ion-Responsive Color-Tunable Emitting Insulated π-Conjugated Polymer Film.

Angewandte Chemie (International ed. in English)

Hosomi T, Masai H, Fujihara T, Tsuji Y, Terao J.
PMID: 27383238
Angew Chem Int Ed Engl. 2016 Oct 17;55(43):13427-13431. doi: 10.1002/anie.201603160. Epub 2016 Jul 07.

We report the synthesis of an insulated π-conjugated polymer containing 2,2'-bipyridine moieties as metal coordination sites. Metal coordination to the polymer enabled easy and reversible tuning of the luminescent color without changes to the main chain skeleton. The permethylated...

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Hosomi T, Masai H, Fujihara T, et al. A Typical Metal-Ion-Responsive Color-Tunable Emitting Insulated π-Conjugated Polymer Film. Angew Chem Int Ed Engl. 2016;55(43):13427-13431doi: 10.1002/anie.201603160.
Hosomi, T., Masai, H., Fujihara, T., Tsuji, Y., & Terao, J. (2016). A Typical Metal-Ion-Responsive Color-Tunable Emitting Insulated π-Conjugated Polymer Film. Angewandte Chemie (International ed. in English), 55(43), 13427-13431. https://doi.org/10.1002/anie.201603160
Hosomi, Takuro, et al. "A Typical Metal-Ion-Responsive Color-Tunable Emitting Insulated π-Conjugated Polymer Film." Angewandte Chemie (International ed. in English) vol. 55,43 (2016): 13427-13431. doi: https://doi.org/10.1002/anie.201603160
Hosomi T, Masai H, Fujihara T, Tsuji Y, Terao J. A Typical Metal-Ion-Responsive Color-Tunable Emitting Insulated π-Conjugated Polymer Film. Angew Chem Int Ed Engl. 2016 Oct 17;55(43):13427-13431. doi: 10.1002/anie.201603160. Epub 2016 Jul 07. PMID: 27383238.
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Coupling of spatially partially coherent beams into planar waveguides.

Optics express

Partanen H, Tervo J, Turunen J.
PMID: 25837126
Opt Express. 2015 Mar 23;23(6):7879-93. doi: 10.1364/OE.23.007879.

The second-order coherence theory of partially spatially coherent light and the overlap integral method are applied to study the end-coupling of stationary multimode light beams into planar waveguides. A method is presented for the determination of the cross-spectral density...

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Partanen H, Tervo J, Turunen J. Coupling of spatially partially coherent beams into planar waveguides. Opt Express. 2015;23(6):7879-93doi: 10.1364/OE.23.007879.
Partanen, H., Tervo, J., & Turunen, J. (2015). Coupling of spatially partially coherent beams into planar waveguides. Optics express, 23(6), 7879-93. https://doi.org/10.1364/OE.23.007879
Partanen, Henri, et al. "Coupling of spatially partially coherent beams into planar waveguides." Optics express vol. 23,6 (2015): 7879-93. doi: https://doi.org/10.1364/OE.23.007879
Partanen H, Tervo J, Turunen J. Coupling of spatially partially coherent beams into planar waveguides. Opt Express. 2015 Mar 23;23(6):7879-93. doi: 10.1364/OE.23.007879. PMID: 25837126.
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Imaging with partially coherent light: elementary-field approach.

Optics express

Singh M, Lajunen H, Tervo J, Turunen J.
PMID: 26561084
Opt Express. 2015 Nov 02;23(22):28132-40. doi: 10.1364/OE.23.028132.

Numerical modeling of bright-field and dark-field imaging with spatially partially coherent light is considered. The illuminating field is expressed as a superposition of transversely shifted fully coherent elementary fields of identical form. Examples of imaging under variable coherence conditions...

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Singh M, Lajunen H, Tervo J, et al. Imaging with partially coherent light: elementary-field approach. Opt Express. 2015;23(22):28132-40doi: 10.1364/OE.23.028132.
Singh, M., Lajunen, H., Tervo, J., & Turunen, J. (2015). Imaging with partially coherent light: elementary-field approach. Optics express, 23(22), 28132-40. https://doi.org/10.1364/OE.23.028132
Singh, Manisha, et al. "Imaging with partially coherent light: elementary-field approach." Optics express vol. 23,22 (2015): 28132-40. doi: https://doi.org/10.1364/OE.23.028132
Singh M, Lajunen H, Tervo J, Turunen J. Imaging with partially coherent light: elementary-field approach. Opt Express. 2015 Nov 02;23(22):28132-40. doi: 10.1364/OE.23.028132. PMID: 26561084.
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Nickel-catalyzed cross-coupling reaction of grignard reagents with alkyl halides and tosylates: remarkable effect of 1,3-butadienes.

Journal of the American Chemical Society

Terao J, Watanabe H, Ikumi A, Kuniyasu H, Kambe N.
PMID: 11960446
J Am Chem Soc. 2002 Apr 24;124(16):4222-3. doi: 10.1021/ja025828v.

A new method for the cross-coupling reaction of Grignard reagents with alkyl chlorides, bromides, and tosylates has been developed by the use of a nickel catalyst in the presence of a diene as an additive. This reaction proceeds efficiently...

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Terao J, Watanabe H, Ikumi A, et al. Nickel-catalyzed cross-coupling reaction of grignard reagents with alkyl halides and tosylates: remarkable effect of 1,3-butadienes. J Am Chem Soc. 2002;124(16):4222-3doi: 10.1021/ja025828v.
Terao, J., Watanabe, H., Ikumi, A., Kuniyasu, H., & Kambe, N. (2002). Nickel-catalyzed cross-coupling reaction of grignard reagents with alkyl halides and tosylates: remarkable effect of 1,3-butadienes. Journal of the American Chemical Society, 124(16), 4222-3. https://doi.org/10.1021/ja025828v
Terao, Jun, et al. "Nickel-catalyzed cross-coupling reaction of grignard reagents with alkyl halides and tosylates: remarkable effect of 1,3-butadienes." Journal of the American Chemical Society vol. 124,16 (2002): 4222-3. doi: https://doi.org/10.1021/ja025828v
Terao J, Watanabe H, Ikumi A, Kuniyasu H, Kambe N. Nickel-catalyzed cross-coupling reaction of grignard reagents with alkyl halides and tosylates: remarkable effect of 1,3-butadienes. J Am Chem Soc. 2002 Apr 24;124(16):4222-3. doi: 10.1021/ja025828v. PMID: 11960446.
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Showing 1 to 12 of 280 entries