Advanced Search
Display options
Filter resources
Text Availability
Article type
Publication date
Species
Language
Sex
Age
Showing 1 to 12 of 309 entries
Sorted by: Best Match Show Resources per page
Breaking bad news of cancer diagnosis - Perception of the cancer patients in a rural community in Malaysia.

South Asian journal of cancer

Bain MG, Lian CW, Thon CC.
PMID: 24818107
South Asian J Cancer. 2014 Apr;3(2):116-21. doi: 10.4103/2278-330X.130447.

CONTEXT: Breaking of bad news is an important component in the management of cancer patients.AIMS: This study aimed to assess the perceptions of breaking bad news of cancer diagnosis.SETTINGS AND DESIGN: It was a cross-sectional study using Breaking Bad...

Cite
Bain MG, Lian CW, Thon CC. Breaking bad news of cancer diagnosis - Perception of the cancer patients in a rural community in Malaysia. South Asian J Cancer. 2014;3(2):116-21doi: 10.4103/2278-330X.130447.
Bain, M. G., Lian, C. W., & Thon, C. C. (2014). Breaking bad news of cancer diagnosis - Perception of the cancer patients in a rural community in Malaysia. South Asian journal of cancer, 3(2), 116-21. https://doi.org/10.4103/2278-330X.130447
Bain, Mathew Gabriel, et al. "Breaking bad news of cancer diagnosis - Perception of the cancer patients in a rural community in Malaysia." South Asian journal of cancer vol. 3,2 (2014): 116-21. doi: https://doi.org/10.4103/2278-330X.130447
Bain MG, Lian CW, Thon CC. Breaking bad news of cancer diagnosis - Perception of the cancer patients in a rural community in Malaysia. South Asian J Cancer. 2014 Apr;3(2):116-21. doi: 10.4103/2278-330X.130447. PMID: 24818107; PMCID: PMC4014642.
Copy Download .nbib Format: NLM
Why is the Ir(III)-Mediated Amido Transfer Much Faster Than the Rh(III)-Mediated Reaction? A Combined Experimental and Computational Study.

Journal of the American Chemical Society

Park Y, Heo J, Baik MH, Chang S.
PMID: 27690406
J Am Chem Soc. 2016 Oct 26;138(42):14020-14029. doi: 10.1021/jacs.6b08211. Epub 2016 Oct 13.

The mechanism of the Ir(III)- and Rh(III)-mediated C-N coupling reaction, which is the key step for catalytic C-H amidation, was investigated in an integrated experimental and computational study. Novel amidating agents containing a 1,4,2-dioxazole moiety allowed for designing a...

Cite
Park Y, Heo J, Baik MH, et al. Why is the Ir(III)-Mediated Amido Transfer Much Faster Than the Rh(III)-Mediated Reaction? A Combined Experimental and Computational Study. J Am Chem Soc. 2016;138(42):14020-14029doi: 10.1021/jacs.6b08211.
Park, Y., Heo, J., Baik, M. H., & Chang, S. (2016). Why is the Ir(III)-Mediated Amido Transfer Much Faster Than the Rh(III)-Mediated Reaction? A Combined Experimental and Computational Study. Journal of the American Chemical Society, 138(42), 14020-14029. https://doi.org/10.1021/jacs.6b08211
Park, Yoonsu, et al. "Why is the Ir(III)-Mediated Amido Transfer Much Faster Than the Rh(III)-Mediated Reaction? A Combined Experimental and Computational Study." Journal of the American Chemical Society vol. 138,42 (2016): 14020-14029. doi: https://doi.org/10.1021/jacs.6b08211
Park Y, Heo J, Baik MH, Chang S. Why is the Ir(III)-Mediated Amido Transfer Much Faster Than the Rh(III)-Mediated Reaction? A Combined Experimental and Computational Study. J Am Chem Soc. 2016 Oct 26;138(42):14020-14029. doi: 10.1021/jacs.6b08211. Epub 2016 Oct 13. PMID: 27690406.
Copy Download .nbib Format: NLM
Structural elucidation of a mononuclear titanium methylidene.

Chemical communications (Cambridge, England)

Grant LN, Ahn S, Manor BC, Baik MH, Mindiola DJ.
PMID: 28246666
Chem Commun (Camb). 2017 Mar 25;53(24):3415-3417. doi: 10.1039/c7cc00654c. Epub 2017 Mar 01.

The first example of a structurally characterized titanium methylidene, (PN)

Cite
Grant LN, Ahn S, Manor BC, et al. Structural elucidation of a mononuclear titanium methylidene. Chem Commun (Camb). 2017;53(24):3415-3417doi: 10.1039/c7cc00654c.
Grant, L. N., Ahn, S., Manor, B. C., Baik, M. H., & Mindiola, D. J. (2017). Structural elucidation of a mononuclear titanium methylidene. Chemical communications (Cambridge, England), 53(24), 3415-3417. https://doi.org/10.1039/c7cc00654c
Grant, Lauren N, et al. "Structural elucidation of a mononuclear titanium methylidene." Chemical communications (Cambridge, England) vol. 53,24 (2017): 3415-3417. doi: https://doi.org/10.1039/c7cc00654c
Grant LN, Ahn S, Manor BC, Baik MH, Mindiola DJ. Structural elucidation of a mononuclear titanium methylidene. Chem Commun (Camb). 2017 Mar 25;53(24):3415-3417. doi: 10.1039/c7cc00654c. Epub 2017 Mar 01. PMID: 28246666.
Copy Download .nbib Format: NLM
Mechanistic Studies of Bismuth(V)-Mediated Thioglycoside Activation Reveal Differential Reactivity of Anomers.

The Journal of organic chemistry

Goswami M, Ashley DC, Baik MH, Pohl NL.
PMID: 27295299
J Org Chem. 2016 Jul 15;81(14):5949-62. doi: 10.1021/acs.joc.6b00860. Epub 2016 Jun 24.

The mechanism of bismuth(V)-mediated thioglycoside activation was examined using reaction kinetics and quantum chemical reaction models. NMR experiments show an unusual nonlinear growth/decay curve for the glycosylation reaction. Further studies suggest an anomeric inversion of the β-glycoside donor to...

Cite
Goswami M, Ashley DC, Baik MH, et al. Mechanistic Studies of Bismuth(V)-Mediated Thioglycoside Activation Reveal Differential Reactivity of Anomers. J Org Chem. 2016;81(14):5949-62doi: 10.1021/acs.joc.6b00860.
Goswami, M., Ashley, D. C., Baik, M. H., & Pohl, N. L. (2016). Mechanistic Studies of Bismuth(V)-Mediated Thioglycoside Activation Reveal Differential Reactivity of Anomers. The Journal of organic chemistry, 81(14), 5949-62. https://doi.org/10.1021/acs.joc.6b00860
Goswami, Manibarsha, et al. "Mechanistic Studies of Bismuth(V)-Mediated Thioglycoside Activation Reveal Differential Reactivity of Anomers." The Journal of organic chemistry vol. 81,14 (2016): 5949-62. doi: https://doi.org/10.1021/acs.joc.6b00860
Goswami M, Ashley DC, Baik MH, Pohl NL. Mechanistic Studies of Bismuth(V)-Mediated Thioglycoside Activation Reveal Differential Reactivity of Anomers. J Org Chem. 2016 Jul 15;81(14):5949-62. doi: 10.1021/acs.joc.6b00860. Epub 2016 Jun 24. PMID: 27295299.
Copy Download .nbib Format: NLM
A diastereoselective metal-catalyzed [2+2] cycloaddition of bis-enomes.

Journal of the American Chemical Society

Baik TG, Luis AL, Wang LC, Krische MJ.
PMID: 11439068
J Am Chem Soc. 2001 Jul 11;123(27):6716-7. doi: 10.1021/ja010800p.

No abstract available.

Cite
Baik TG, Luis AL, Wang LC, et al. A diastereoselective metal-catalyzed [2+2] cycloaddition of bis-enomes. J Am Chem Soc. 2001;123(27):6716-7doi: 10.1021/ja010800p.
Baik, T. G., Luis, A. L., Wang, L. C., & Krische, M. J. (2001). A diastereoselective metal-catalyzed [2+2] cycloaddition of bis-enomes. Journal of the American Chemical Society, 123(27), 6716-7. https://doi.org/10.1021/ja010800p
Baik, T G, et al. "A diastereoselective metal-catalyzed [2+2] cycloaddition of bis-enomes." Journal of the American Chemical Society vol. 123,27 (2001): 6716-7. doi: https://doi.org/10.1021/ja010800p
Baik TG, Luis AL, Wang LC, Krische MJ. A diastereoselective metal-catalyzed [2+2] cycloaddition of bis-enomes. J Am Chem Soc. 2001 Jul 11;123(27):6716-7. doi: 10.1021/ja010800p. PMID: 11439068.
Copy Download .nbib Format: NLM
Electronic structure of the water-oxidation catalyst [(bpy)2(OHx)RuORu(OHy)(bpy)2]z+: weak coupling between the metal centers is preferred over strong coupling.

Journal of the American Chemical Society

Yang X, Baik MH.
PMID: 15479066
J Am Chem Soc. 2004 Oct 20;126(41):13222-3. doi: 10.1021/ja0462427.

High-level DFT calculations indicate that the singlet ground state of the water-oxidizing blue Ru dimer [(bpy)2(OH2)RuIIIORuIII(OH2)(bpy)2]4+ is not due to a strong coupling of the excess electrons from each of the low-spin d5 RuIII centers across the Ru-O-Ru moiety,...

Cite
Yang X, Baik MH. Electronic structure of the water-oxidation catalyst [(bpy)2(OHx)RuORu(OHy)(bpy)2]z+: weak coupling between the metal centers is preferred over strong coupling. J Am Chem Soc. 2004;126(41):13222-3doi: 10.1021/ja0462427.
Yang, X., & Baik, M. H. (2004). Electronic structure of the water-oxidation catalyst [(bpy)2(OHx)RuORu(OHy)(bpy)2]z+: weak coupling between the metal centers is preferred over strong coupling. Journal of the American Chemical Society, 126(41), 13222-3. https://doi.org/10.1021/ja0462427
Yang, Xiaofan, and Baik, Mu-Hyun. "Electronic structure of the water-oxidation catalyst [(bpy)2(OHx)RuORu(OHy)(bpy)2]z+: weak coupling between the metal centers is preferred over strong coupling." Journal of the American Chemical Society vol. 126,41 (2004): 13222-3. doi: https://doi.org/10.1021/ja0462427
Yang X, Baik MH. Electronic structure of the water-oxidation catalyst [(bpy)2(OHx)RuORu(OHy)(bpy)2]z+: weak coupling between the metal centers is preferred over strong coupling. J Am Chem Soc. 2004 Oct 20;126(41):13222-3. doi: 10.1021/ja0462427. PMID: 15479066.
Copy Download .nbib Format: NLM
Assembly of polymer/lipid composite films on solids based on hairy rod LB-films.

European biophysics journal : EBJ

Sigl H, Brink G, Seufert M, Schulz M, Wegner G, Sackmann E.
PMID: 21188573
Eur Biophys J. 1997;25(4):249-59. doi: 10.1007/s002490050037.

The present work deals with the assembly of multilayers or rod-like polymers with hydrophobic side chains (called hairy rods) and their potential application as ultrathin polymer cushions for the build-up of self healing supported membranes on various solids (Si/SiO(2)-wafer,...

Cite
Sigl H, Brink G, Seufert M, et al. Assembly of polymer/lipid composite films on solids based on hairy rod LB-films. Eur Biophys J. 1997;25(4):249-59doi: 10.1007/s002490050037.
Sigl, H., Brink, G., Seufert, M., Schulz, M., Wegner, G., & Sackmann, E. (1997). Assembly of polymer/lipid composite films on solids based on hairy rod LB-films. European biophysics journal : EBJ, 25(4), 249-59. https://doi.org/10.1007/s002490050037
Sigl, H, et al. "Assembly of polymer/lipid composite films on solids based on hairy rod LB-films." European biophysics journal : EBJ vol. 25,4 (1997): 249-59. doi: https://doi.org/10.1007/s002490050037
Sigl H, Brink G, Seufert M, Schulz M, Wegner G, Sackmann E. Assembly of polymer/lipid composite films on solids based on hairy rod LB-films. Eur Biophys J. 1997;25(4):249-59. doi: 10.1007/s002490050037. PMID: 21188573.
Copy Download .nbib Format: NLM
The mechanism of O-O bond formation in Tanaka's water oxidation catalyst.

Angewandte Chemie (International ed. in English)

Ghosh S, Baik MH.
PMID: 22213120
Angew Chem Int Ed Engl. 2012 Jan 27;51(5):1221-4. doi: 10.1002/anie.201106337. Epub 2011 Dec 23.

No abstract available.

Cite
Ghosh S, Baik MH. The mechanism of O-O bond formation in Tanaka's water oxidation catalyst. Angew Chem Int Ed Engl. 2011;51(5):1221-4doi: 10.1002/anie.201106337.
Ghosh, S., & Baik, M. H. (2012). The mechanism of O-O bond formation in Tanaka's water oxidation catalyst. Angewandte Chemie (International ed. in English), 51(5), 1221-4. https://doi.org/10.1002/anie.201106337
Ghosh, Soumya, and Baik, Mu-Hyun. "The mechanism of O-O bond formation in Tanaka's water oxidation catalyst." Angewandte Chemie (International ed. in English) vol. 51,5 (2012): 1221-4. doi: https://doi.org/10.1002/anie.201106337
Ghosh S, Baik MH. The mechanism of O-O bond formation in Tanaka's water oxidation catalyst. Angew Chem Int Ed Engl. 2012 Jan 27;51(5):1221-4. doi: 10.1002/anie.201106337. Epub 2011 Dec 23. PMID: 22213120.
Copy Download .nbib Format: NLM
Visible-Light-Induced Pyridylation of Remote C(sp.

Angewandte Chemie (International ed. in English)

Kim I, Park B, Kang G, Kim J, Jung H, Lee H, Baik MH, Hong S.
PMID: 30277296
Angew Chem Int Ed Engl. 2018 Nov 19;57(47):15517-15522. doi: 10.1002/anie.201809879. Epub 2018 Oct 23.

Metal-free, visible-light-induced site-selective heteroarylation of remote C(sp

Cite
Kim I, Park B, Kang G, et al. Visible-Light-Induced Pyridylation of Remote C(sp. Angew Chem Int Ed Engl. 2018;57(47):15517-15522doi: 10.1002/anie.201809879.
Kim, I., Park, B., Kang, G., Kim, J., Jung, H., Lee, H., Baik, M. H., & Hong, S. (2018). Visible-Light-Induced Pyridylation of Remote C(sp. Angewandte Chemie (International ed. in English), 57(47), 15517-15522. https://doi.org/10.1002/anie.201809879
Kim, Inwon, et al. "Visible-Light-Induced Pyridylation of Remote C(sp." Angewandte Chemie (International ed. in English) vol. 57,47 (2018): 15517-15522. doi: https://doi.org/10.1002/anie.201809879
Kim I, Park B, Kang G, Kim J, Jung H, Lee H, Baik MH, Hong S. Visible-Light-Induced Pyridylation of Remote C(sp. Angew Chem Int Ed Engl. 2018 Nov 19;57(47):15517-15522. doi: 10.1002/anie.201809879. Epub 2018 Oct 23. PMID: 30277296.
Copy Download .nbib Format: NLM
Reductive Carbocyclization of Homoallylic Alcohols to syn-Cyclobutanes by a Boron-Catalyzed Dual Ring-Closing Pathway.

Angewandte Chemie (International ed. in English)

Hazra CK, Jeong J, Kim H, Baik MH, Park S, Chang S.
PMID: 29327487
Angew Chem Int Ed Engl. 2018 Mar 01;57(10):2692-2696. doi: 10.1002/anie.201713285. Epub 2018 Feb 05.

The organoborane-catalyzed reductive carbocyclization of homoallylic alcohols has been developed by using hydrosilanes as reducing reagents to provide a range of 1,2-disubstituted arylcyclobutanes. The reaction proceeds in a cis-selective manner with high efficiency under mild conditions. Mechanistic studies, including...

Cite
Hazra CK, Jeong J, Kim H, et al. Reductive Carbocyclization of Homoallylic Alcohols to syn-Cyclobutanes by a Boron-Catalyzed Dual Ring-Closing Pathway. Angew Chem Int Ed Engl. 2018;57(10):2692-2696doi: 10.1002/anie.201713285.
Hazra, C. K., Jeong, J., Kim, H., Baik, M. H., Park, S., & Chang, S. (2018). Reductive Carbocyclization of Homoallylic Alcohols to syn-Cyclobutanes by a Boron-Catalyzed Dual Ring-Closing Pathway. Angewandte Chemie (International ed. in English), 57(10), 2692-2696. https://doi.org/10.1002/anie.201713285
Hazra, Chinmoy Kumar, et al. "Reductive Carbocyclization of Homoallylic Alcohols to syn-Cyclobutanes by a Boron-Catalyzed Dual Ring-Closing Pathway." Angewandte Chemie (International ed. in English) vol. 57,10 (2018): 2692-2696. doi: https://doi.org/10.1002/anie.201713285
Hazra CK, Jeong J, Kim H, Baik MH, Park S, Chang S. Reductive Carbocyclization of Homoallylic Alcohols to syn-Cyclobutanes by a Boron-Catalyzed Dual Ring-Closing Pathway. Angew Chem Int Ed Engl. 2018 Mar 01;57(10):2692-2696. doi: 10.1002/anie.201713285. Epub 2018 Feb 05. PMID: 29327487.
Copy Download .nbib Format: NLM
Understanding the Origin of the Regioselectivity in Cyclopolymerizations of Diynes and How to Completely Switch It.

Journal of the American Chemical Society

Jung H, Jung K, Hong M, Kwon S, Kim K, Hong SH, Choi TL, Baik MH.
PMID: 29277991
J Am Chem Soc. 2018 Jan 17;140(2):834-841. doi: 10.1021/jacs.7b11968. Epub 2018 Jan 05.

Grubbs-type olefin metathesis catalysts are known to cyclopolymerize 1,6-heptadiynes to afford conjugated polyenes containing five- or six-membered carbocycles. Although high levels of regioselectivity up to >99:1 were observed previously for the formation of five-membered rings, it was neither possible...

Cite
Jung H, Jung K, Hong M, et al. Understanding the Origin of the Regioselectivity in Cyclopolymerizations of Diynes and How to Completely Switch It. J Am Chem Soc. 2018;140(2):834-841doi: 10.1021/jacs.7b11968.
Jung, H., Jung, K., Hong, M., Kwon, S., Kim, K., Hong, S. H., Choi, T. L., & Baik, M. H. (2018). Understanding the Origin of the Regioselectivity in Cyclopolymerizations of Diynes and How to Completely Switch It. Journal of the American Chemical Society, 140(2), 834-841. https://doi.org/10.1021/jacs.7b11968
Jung, Hoimin, et al. "Understanding the Origin of the Regioselectivity in Cyclopolymerizations of Diynes and How to Completely Switch It." Journal of the American Chemical Society vol. 140,2 (2018): 834-841. doi: https://doi.org/10.1021/jacs.7b11968
Jung H, Jung K, Hong M, Kwon S, Kim K, Hong SH, Choi TL, Baik MH. Understanding the Origin of the Regioselectivity in Cyclopolymerizations of Diynes and How to Completely Switch It. J Am Chem Soc. 2018 Jan 17;140(2):834-841. doi: 10.1021/jacs.7b11968. Epub 2018 Jan 05. PMID: 29277991.
Copy Download .nbib Format: NLM
Rheological properties of rice flour treated with mild solutions of citric acid.

Food science and biotechnology

Jung HJ, Choi HW, Kim BY, Baik MY.
PMID: 30263519
Food Sci Biotechnol. 2017 Feb 28;26(1):129-134. doi: 10.1007/s10068-017-0017-2. eCollection 2017.

Effects of milling methods and organic acids treatments on rheological properties of rice flour were investigated. The average particle-size of wet-milled rice flour was lower and showed lower pasting temperature, peak viscosity, and storage modulus values than those of...

Cite
Jung HJ, Choi HW, Kim BY, et al. Rheological properties of rice flour treated with mild solutions of citric acid. Food Sci Biotechnol. 2017;26(1):129-134doi: 10.1007/s10068-017-0017-2.
Jung, H. J., Choi, H. W., Kim, B. Y., & Baik, M. Y. (2017). Rheological properties of rice flour treated with mild solutions of citric acid. Food science and biotechnology, 26(1), 129-134. https://doi.org/10.1007/s10068-017-0017-2
Jung, Hee-Jung, et al. "Rheological properties of rice flour treated with mild solutions of citric acid." Food science and biotechnology vol. 26,1 (2017): 129-134. doi: https://doi.org/10.1007/s10068-017-0017-2
Jung HJ, Choi HW, Kim BY, Baik MY. Rheological properties of rice flour treated with mild solutions of citric acid. Food Sci Biotechnol. 2017 Feb 28;26(1):129-134. doi: 10.1007/s10068-017-0017-2. eCollection 2017. PMID: 30263519; PMCID: PMC6049468.
Copy Download .nbib Format: NLM
Showing 1 to 12 of 309 entries