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Stereospecific Synthesis of Tetrahydronaphtho[2,3-b]furans Enabled by a Nickel-Promoted Tandem Reductive Cyclization.

Organic letters

Peng Y, Xiao J, Xu XB, Duan SM, Ren L, Shao YL, Wang YW.
PMID: 27658859
Org Lett. 2016 Oct 07;18(19):5170-5173. doi: 10.1021/acs.orglett.6b02665. Epub 2016 Sep 23.

A Ni-mediated cascade to a stereoselective synthesis of trans-tetrahydronaphtho[2,3-b]furans is efficiently achieved for the first time. The mild reductive system can be easily generated from inexpensive and air-stable materials and shows a broad positional tolerance of substituents that were...

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Peng Y, Xiao J, Xu XB, et al. Stereospecific Synthesis of Tetrahydronaphtho[2,3-b]furans Enabled by a Nickel-Promoted Tandem Reductive Cyclization. Org Lett. 2016;18(19):5170-5173doi: 10.1021/acs.orglett.6b02665.
Peng, Y., Xiao, J., Xu, X. B., Duan, S. M., Ren, L., Shao, Y. L., & Wang, Y. W. (2016). Stereospecific Synthesis of Tetrahydronaphtho[2,3-b]furans Enabled by a Nickel-Promoted Tandem Reductive Cyclization. Organic letters, 18(19), 5170-5173. https://doi.org/10.1021/acs.orglett.6b02665
Peng, Yu, et al. "Stereospecific Synthesis of Tetrahydronaphtho[2,3-b]furans Enabled by a Nickel-Promoted Tandem Reductive Cyclization." Organic letters vol. 18,19 (2016): 5170-5173. doi: https://doi.org/10.1021/acs.orglett.6b02665
Peng Y, Xiao J, Xu XB, Duan SM, Ren L, Shao YL, Wang YW. Stereospecific Synthesis of Tetrahydronaphtho[2,3-b]furans Enabled by a Nickel-Promoted Tandem Reductive Cyclization. Org Lett. 2016 Oct 07;18(19):5170-5173. doi: 10.1021/acs.orglett.6b02665. Epub 2016 Sep 23. PMID: 27658859.
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Kinetic and Thermodynamic Control of Structure Transformations in a Family of Cobalt(II)-Organic Frameworks.

ACS applied materials & interfaces

Chen Q, Feng R, Xu J, Jia YY, Wang TT, Chang Z, Bu XH.
PMID: 28920665
ACS Appl Mater Interfaces. 2017 Oct 11;9(40):35141-35149. doi: 10.1021/acsami.7b12925. Epub 2017 Oct 02.

Dynamic metal-organic frameworks (MOFs) that respond to external stimuli have recently attracted great attention. However, the subtle control of dynamic processes as well as the illustration of the underlying mechanism, which is crucial for the targeted construction and modulation...

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Chen Q, Feng R, Xu J, et al. Kinetic and Thermodynamic Control of Structure Transformations in a Family of Cobalt(II)-Organic Frameworks. ACS Appl Mater Interfaces. 2017;9(40):35141-35149doi: 10.1021/acsami.7b12925.
Chen, Q., Feng, R., Xu, J., Jia, Y. Y., Wang, T. T., Chang, Z., & Bu, X. H. (2017). Kinetic and Thermodynamic Control of Structure Transformations in a Family of Cobalt(II)-Organic Frameworks. ACS applied materials & interfaces, 9(40), 35141-35149. https://doi.org/10.1021/acsami.7b12925
Chen, Qiang, et al. "Kinetic and Thermodynamic Control of Structure Transformations in a Family of Cobalt(II)-Organic Frameworks." ACS applied materials & interfaces vol. 9,40 (2017): 35141-35149. doi: https://doi.org/10.1021/acsami.7b12925
Chen Q, Feng R, Xu J, Jia YY, Wang TT, Chang Z, Bu XH. Kinetic and Thermodynamic Control of Structure Transformations in a Family of Cobalt(II)-Organic Frameworks. ACS Appl Mater Interfaces. 2017 Oct 11;9(40):35141-35149. doi: 10.1021/acsami.7b12925. Epub 2017 Oct 02. PMID: 28920665.
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DBU-promoted carboxylative cyclization of o-hydroxy- and o-acetamidoacetophenone.

Beilstein journal of organic chemistry

Zhang WZ, Liu S, Lu XB.
PMID: 26124893
Beilstein J Org Chem. 2015 May 29;11:906-12. doi: 10.3762/bjoc.11.102. eCollection 2015.

The carboxylative cyclization of o-hydroxy- and o-acetamidoacetophenone with carbon dioxide promoted by the organic base 1,8-diazabicycloundec-7-ene (DBU) is reported. This reaction provides convenient access to the biologically important compounds 4-hydroxy-2H-chromen-2-one and 4-hydroxy-2(1H)-quinolinone in moderate to good yields using carbon...

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Zhang WZ, Liu S, Lu XB. DBU-promoted carboxylative cyclization of o-hydroxy- and o-acetamidoacetophenone. Beilstein J Org Chem. 2015;11:906-12doi: 10.3762/bjoc.11.102.
Zhang, W. Z., Liu, S., & Lu, X. B. (2015). DBU-promoted carboxylative cyclization of o-hydroxy- and o-acetamidoacetophenone. Beilstein journal of organic chemistry, 11906-12. https://doi.org/10.3762/bjoc.11.102
Zhang, Wen-Zhen, et al. "DBU-promoted carboxylative cyclization of o-hydroxy- and o-acetamidoacetophenone." Beilstein journal of organic chemistry vol. 11 (2015): 906-12. doi: https://doi.org/10.3762/bjoc.11.102
Zhang WZ, Liu S, Lu XB. DBU-promoted carboxylative cyclization of o-hydroxy- and o-acetamidoacetophenone. Beilstein J Org Chem. 2015 May 29;11:906-12. doi: 10.3762/bjoc.11.102. eCollection 2015. PMID: 26124893; PMCID: PMC4464362.
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A heterometallic strategy to achieve a large magnetocaloric effect in polymeric 3d complexes.

Chemical communications (Cambridge, England)

Zhao JP, Han SD, Jiang X, Liu SJ, Zhao R, Chang Z, Bu XH.
PMID: 25877906
Chem Commun (Camb). 2015 May 14;51(39):8288-91. doi: 10.1039/c5cc00915d.

Metal formate frameworks [A][CrMn(HCOO)6] (A = CH3NH2CH3(+) for 1 and CH3NH3(+) for 2) with a large MCE were obtained, directed by the heterometallic strategy in which very weak magnetic interactions were achieved. A switch from antiferromagnetism to ferromagnetism occurs...

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Zhao JP, Han SD, Jiang X, et al. A heterometallic strategy to achieve a large magnetocaloric effect in polymeric 3d complexes. Chem Commun (Camb). 2015;51(39):8288-91doi: 10.1039/c5cc00915d.
Zhao, J. P., Han, S. D., Jiang, X., Liu, S. J., Zhao, R., Chang, Z., & Bu, X. H. (2015). A heterometallic strategy to achieve a large magnetocaloric effect in polymeric 3d complexes. Chemical communications (Cambridge, England), 51(39), 8288-91. https://doi.org/10.1039/c5cc00915d
Zhao, Jiong-Peng, et al. "A heterometallic strategy to achieve a large magnetocaloric effect in polymeric 3d complexes." Chemical communications (Cambridge, England) vol. 51,39 (2015): 8288-91. doi: https://doi.org/10.1039/c5cc00915d
Zhao JP, Han SD, Jiang X, Liu SJ, Zhao R, Chang Z, Bu XH. A heterometallic strategy to achieve a large magnetocaloric effect in polymeric 3d complexes. Chem Commun (Camb). 2015 May 14;51(39):8288-91. doi: 10.1039/c5cc00915d. PMID: 25877906.
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Copper-Catalyzed Cross-Coupling Reaction of Allyl Boron Ester with 1°/2°/3°-Halogenated Alkanes.

Organic letters

Wang GZ, Jiang J, Bu XS, Dai JJ, Xu J, Fu Y, Xu HJ.
PMID: 26181828
Org Lett. 2015 Aug 07;17(15):3682-5. doi: 10.1021/acs.orglett.5b01612. Epub 2015 Jul 16.

The cross-coupling reaction of allyl boron ester with 1°/2°/3°-halogenated alkanes in the presence of copper has been developed for the first time, which provides a mild and efficient method for the construction of saturated C(sp(3))-C(sp(3)) bonds. This protocol shows...

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Wang GZ, Jiang J, Bu XS, et al. Copper-Catalyzed Cross-Coupling Reaction of Allyl Boron Ester with 1°/2°/3°-Halogenated Alkanes. Org Lett. 2015;17(15):3682-5doi: 10.1021/acs.orglett.5b01612.
Wang, G. Z., Jiang, J., Bu, X. S., Dai, J. J., Xu, J., Fu, Y., & Xu, H. J. (2015). Copper-Catalyzed Cross-Coupling Reaction of Allyl Boron Ester with 1°/2°/3°-Halogenated Alkanes. Organic letters, 17(15), 3682-5. https://doi.org/10.1021/acs.orglett.5b01612
Wang, Guang-Zu, et al. "Copper-Catalyzed Cross-Coupling Reaction of Allyl Boron Ester with 1°/2°/3°-Halogenated Alkanes." Organic letters vol. 17,15 (2015): 3682-5. doi: https://doi.org/10.1021/acs.orglett.5b01612
Wang GZ, Jiang J, Bu XS, Dai JJ, Xu J, Fu Y, Xu HJ. Copper-Catalyzed Cross-Coupling Reaction of Allyl Boron Ester with 1°/2°/3°-Halogenated Alkanes. Org Lett. 2015 Aug 07;17(15):3682-5. doi: 10.1021/acs.orglett.5b01612. Epub 2015 Jul 16. PMID: 26181828.
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Pore space partition by symmetry-matching regulated ligand insertion and dramatic tuning on carbon dioxide uptake.

Journal of the American Chemical Society

Zhao X, Bu X, Zhai QG, Tran H, Feng P.
PMID: 25621414
J Am Chem Soc. 2015 Feb 04;137(4):1396-9. doi: 10.1021/ja512137t. Epub 2015 Jan 26.

Metal-organic frameworks (MOFs) with the highest CO(2) uptake capacity are usually those equipped with open metal sites. Here we seek alternative strategies and mechanisms for developing high-performance CO(2) adsorbents. We demonstrate that through a ligand insertion pore space partition...

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Zhao X, Bu X, Zhai QG, et al. Pore space partition by symmetry-matching regulated ligand insertion and dramatic tuning on carbon dioxide uptake. J Am Chem Soc. 2015;137(4):1396-9doi: 10.1021/ja512137t.
Zhao, X., Bu, X., Zhai, Q. G., Tran, H., & Feng, P. (2015). Pore space partition by symmetry-matching regulated ligand insertion and dramatic tuning on carbon dioxide uptake. Journal of the American Chemical Society, 137(4), 1396-9. https://doi.org/10.1021/ja512137t
Zhao, Xiang, et al. "Pore space partition by symmetry-matching regulated ligand insertion and dramatic tuning on carbon dioxide uptake." Journal of the American Chemical Society vol. 137,4 (2015): 1396-9. doi: https://doi.org/10.1021/ja512137t
Zhao X, Bu X, Zhai QG, Tran H, Feng P. Pore space partition by symmetry-matching regulated ligand insertion and dramatic tuning on carbon dioxide uptake. J Am Chem Soc. 2015 Feb 04;137(4):1396-9. doi: 10.1021/ja512137t. Epub 2015 Jan 26. PMID: 25621414.
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Concentration-driven phase control for low temperature synthesis of phase-pure anatase and rutile titanium oxide.

Journal of colloid and interface science

Wang Z, Xiao C, Yamada S, Yoshinaga K, Bu XR, Zhang M, Anshari M, Alas Y.
PMID: 25746180
J Colloid Interface Sci. 2015 Jun 15;448:280-6. doi: 10.1016/j.jcis.2015.02.001. Epub 2015 Feb 09.

It is highly desirable to develop controlled synthetic methods at low temperature (

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Wang Z, Xiao C, Yamada S, et al. Concentration-driven phase control for low temperature synthesis of phase-pure anatase and rutile titanium oxide. J Colloid Interface Sci. 2015;448:280-6doi: 10.1016/j.jcis.2015.02.001.
Wang, Z., Xiao, C., Yamada, S., Yoshinaga, K., Bu, X. R., Zhang, M., Anshari, M., & Alas, Y. (2015). Concentration-driven phase control for low temperature synthesis of phase-pure anatase and rutile titanium oxide. Journal of colloid and interface science, 448280-6. https://doi.org/10.1016/j.jcis.2015.02.001
Wang, Zhifeng, et al. "Concentration-driven phase control for low temperature synthesis of phase-pure anatase and rutile titanium oxide." Journal of colloid and interface science vol. 448 (2015): 280-6. doi: https://doi.org/10.1016/j.jcis.2015.02.001
Wang Z, Xiao C, Yamada S, Yoshinaga K, Bu XR, Zhang M, Anshari M, Alas Y. Concentration-driven phase control for low temperature synthesis of phase-pure anatase and rutile titanium oxide. J Colloid Interface Sci. 2015 Jun 15;448:280-6. doi: 10.1016/j.jcis.2015.02.001. Epub 2015 Feb 09. PMID: 25746180.
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Pathway-related modules involved in the application of sevoflurane or propofol in off-pump coronary artery bypass graft surgery.

Experimental and therapeutic medicine

Bu X, Wang B, Wang Y, Wang Z, Gong C, Qi F, Zhang C.
PMID: 28672899
Exp Ther Med. 2017 Jul;14(1):97-106. doi: 10.3892/etm.2017.4504. Epub 2017 May 23.

Off-pump coronary artery bypass graft (CABG) surgery has recently emerged as a means to avoid the sequelae of extracorporeal circulation, including the whole-body inflammatory response, coagulation disorders and multiple organ dysfunction. At present, gas anesthesia, sevoflurane and intravenous anesthesia...

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Bu X, Wang B, Wang Y, et al. Pathway-related modules involved in the application of sevoflurane or propofol in off-pump coronary artery bypass graft surgery. Exp Ther Med. 2017;14(1):97-106doi: 10.3892/etm.2017.4504.
Bu, X., Wang, B., Wang, Y., Wang, Z., Gong, C., Qi, F., & Zhang, C. (2017). Pathway-related modules involved in the application of sevoflurane or propofol in off-pump coronary artery bypass graft surgery. Experimental and therapeutic medicine, 14(1), 97-106. https://doi.org/10.3892/etm.2017.4504
Bu, Xiangmei, et al. "Pathway-related modules involved in the application of sevoflurane or propofol in off-pump coronary artery bypass graft surgery." Experimental and therapeutic medicine vol. 14,1 (2017): 97-106. doi: https://doi.org/10.3892/etm.2017.4504
Bu X, Wang B, Wang Y, Wang Z, Gong C, Qi F, Zhang C. Pathway-related modules involved in the application of sevoflurane or propofol in off-pump coronary artery bypass graft surgery. Exp Ther Med. 2017 Jul;14(1):97-106. doi: 10.3892/etm.2017.4504. Epub 2017 May 23. PMID: 28672899; PMCID: PMC5488504.
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Serum thymidine kinase 1 levels correlate with clinical characteristics of esophageal squamous cell carcinoma.

International journal of clinical and experimental medicine

Ji Y, Wu XB, Chen JY, Hu B, Zhu QK, Zhu XF, Zheng MF.
PMID: 26550200
Int J Clin Exp Med. 2015 Aug 15;8(8):12850-7. eCollection 2015.

Patients with esophageal cancer are often diagnosed at advanced stages, leading to poor prognosis. Biomarkers are needed to enable earlier detection as well as to aid in the prediction of prognosis, but to date these tools remain scarce. Thymidine...

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Ji Y, Wu XB, Chen JY, et al. Serum thymidine kinase 1 levels correlate with clinical characteristics of esophageal squamous cell carcinoma. Int J Clin Exp Med. 2015;8(8):12850-7
Ji, Y., Wu, X. B., Chen, J. Y., Hu, B., Zhu, Q. K., Zhu, X. F., & Zheng, M. F. (2015). Serum thymidine kinase 1 levels correlate with clinical characteristics of esophageal squamous cell carcinoma. International journal of clinical and experimental medicine, 8(8), 12850-7.
Ji, Yong, et al. "Serum thymidine kinase 1 levels correlate with clinical characteristics of esophageal squamous cell carcinoma." International journal of clinical and experimental medicine vol. 8,8 (2015): 12850-7.
Ji Y, Wu XB, Chen JY, Hu B, Zhu QK, Zhu XF, Zheng MF. Serum thymidine kinase 1 levels correlate with clinical characteristics of esophageal squamous cell carcinoma. Int J Clin Exp Med. 2015 Aug 15;8(8):12850-7. eCollection 2015. PMID: 26550200; PMCID: PMC4612885.
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Antibacterial activity and mode of action of totarol against .

Journal of food science and technology

Shi C, Che M, Zhang X, Liu Z, Meng R, Bu X, Ye H, Guo N.
PMID: 29487434
J Food Sci Technol. 2018 Mar;55(3):924-934. doi: 10.1007/s13197-017-3000-2. Epub 2018 Feb 03.

Food contaminated with pathogenic bacteria such as

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Shi C, Che M, Zhang X, et al. Antibacterial activity and mode of action of totarol against . J Food Sci Technol. 2018;55(3):924-934doi: 10.1007/s13197-017-3000-2.
Shi, C., Che, M., Zhang, X., Liu, Z., Meng, R., Bu, X., Ye, H., & Guo, N. (2018). Antibacterial activity and mode of action of totarol against . Journal of food science and technology, 55(3), 924-934. https://doi.org/10.1007/s13197-017-3000-2
Shi, Ce, et al. "Antibacterial activity and mode of action of totarol against ." Journal of food science and technology vol. 55,3 (2018): 924-934. doi: https://doi.org/10.1007/s13197-017-3000-2
Shi C, Che M, Zhang X, Liu Z, Meng R, Bu X, Ye H, Guo N. Antibacterial activity and mode of action of totarol against . J Food Sci Technol. 2018 Mar;55(3):924-934. doi: 10.1007/s13197-017-3000-2. Epub 2018 Feb 03. PMID: 29487434; PMCID: PMC5821648.
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MIL-100 derived nitrogen-embodied carbon shells embedded with iron nanoparticles.

Nanoscale

Mao C, Kong A, Wang Y, Bu X, Feng P.
PMID: 26037013
Nanoscale. 2015 Jun 28;7(24):10817-22. doi: 10.1039/c5nr02346g. Epub 2015 Jun 03.

The use of metal-organic frameworks (MOFs) as templates and precursors to synthesize new carbon materials with controllable morphology and pre-selected heteroatom doping holds promise for applications as efficient non-precious metal catalysts. Here, we report a facile pyrolysis pathway to...

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Mao C, Kong A, Wang Y, et al. MIL-100 derived nitrogen-embodied carbon shells embedded with iron nanoparticles. Nanoscale. 2015;7(24):10817-22doi: 10.1039/c5nr02346g.
Mao, C., Kong, A., Wang, Y., Bu, X., & Feng, P. (2015). MIL-100 derived nitrogen-embodied carbon shells embedded with iron nanoparticles. Nanoscale, 7(24), 10817-22. https://doi.org/10.1039/c5nr02346g
Mao, Chengyu, et al. "MIL-100 derived nitrogen-embodied carbon shells embedded with iron nanoparticles." Nanoscale vol. 7,24 (2015): 10817-22. doi: https://doi.org/10.1039/c5nr02346g
Mao C, Kong A, Wang Y, Bu X, Feng P. MIL-100 derived nitrogen-embodied carbon shells embedded with iron nanoparticles. Nanoscale. 2015 Jun 28;7(24):10817-22. doi: 10.1039/c5nr02346g. Epub 2015 Jun 03. PMID: 26037013.
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Cooperative Crystallization of Heterometallic Indium-Chromium Metal-Organic Polyhedra and Their Fast Proton Conductivity.

Angewandte Chemie (International ed. in English)

Zhai QG, Mao C, Zhao X, Lin Q, Bu F, Chen X, Bu X, Feng P.
PMID: 25981827
Angew Chem Int Ed Engl. 2015 Jun 26;54(27):7886-90. doi: 10.1002/anie.201503095. Epub 2015 May 15.

Metal-organic polyhedra (MOPs) or frameworks (MOFs) based on Cr(3+) are notoriously difficult to synthesize, especially as crystals large enough to be suitable for characterization of the structure or properties. It is now shown that the co-existence of In(3+) and...

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Zhai QG, Mao C, Zhao X, et al. Cooperative Crystallization of Heterometallic Indium-Chromium Metal-Organic Polyhedra and Their Fast Proton Conductivity. Angew Chem Int Ed Engl. 2015;54(27):7886-90doi: 10.1002/anie.201503095.
Zhai, Q. G., Mao, C., Zhao, X., Lin, Q., Bu, F., Chen, X., Bu, X., & Feng, P. (2015). Cooperative Crystallization of Heterometallic Indium-Chromium Metal-Organic Polyhedra and Their Fast Proton Conductivity. Angewandte Chemie (International ed. in English), 54(27), 7886-90. https://doi.org/10.1002/anie.201503095
Zhai, Quan-Guo, et al. "Cooperative Crystallization of Heterometallic Indium-Chromium Metal-Organic Polyhedra and Their Fast Proton Conductivity." Angewandte Chemie (International ed. in English) vol. 54,27 (2015): 7886-90. doi: https://doi.org/10.1002/anie.201503095
Zhai QG, Mao C, Zhao X, Lin Q, Bu F, Chen X, Bu X, Feng P. Cooperative Crystallization of Heterometallic Indium-Chromium Metal-Organic Polyhedra and Their Fast Proton Conductivity. Angew Chem Int Ed Engl. 2015 Jun 26;54(27):7886-90. doi: 10.1002/anie.201503095. Epub 2015 May 15. PMID: 25981827.
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Showing 1 to 12 of 1073 entries