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Hydrogen-bonding alcohol-water interactions in binary ethanol, 1-propanol, and structure II clathrate hydrates

pipeline programs

Alavi S, Takeya S, Woo TK.
GSID: 6h509nW49bIJ
S Alavi, S Takeya, R Ohmura, TK Woo… - The Journal of …, 2010 - aip.scitation.org

The small alcohols ethanol, 1-propanol, and 2-propanol are miscible in water, form strong hydrogen bonds with water molecules, and are usually known as inhibitors for clathrate …

Electrochemical synthesis of carbon nanodots directly from alcohols.

Chemistry (Weinheim an der Bergstrasse, Germany)

Deng J, Lu Q, Mi N, Li H, Liu M, Xu M, Tan L, Xie Q, Zhang Y, Yao S.
PMID: 24623706
Chemistry. 2014 Apr 22;20(17):4993-9. doi: 10.1002/chem.201304869. Epub 2014 Mar 12.

Carbon nanodots (C-dots) show great potential as an important material for biochemical sensing, energy conversion, photocatalysis, and optoelectronics because of their water solubility, chemical inertness, low toxicity, and photo- and electronic properties. Numerous methods have been proposed for the...

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Deng J, Lu Q, Mi N, et al. Electrochemical synthesis of carbon nanodots directly from alcohols. Chemistry. 2014;20(17):4993-9doi: 10.1002/chem.201304869.
Deng, J., Lu, Q., Mi, N., Li, H., Liu, M., Xu, M., Tan, L., Xie, Q., Zhang, Y., & Yao, S. (2014). Electrochemical synthesis of carbon nanodots directly from alcohols. Chemistry (Weinheim an der Bergstrasse, Germany), 20(17), 4993-9. https://doi.org/10.1002/chem.201304869
Deng, Jianhui, et al. "Electrochemical synthesis of carbon nanodots directly from alcohols." Chemistry (Weinheim an der Bergstrasse, Germany) vol. 20,17 (2014): 4993-9. doi: https://doi.org/10.1002/chem.201304869
Deng J, Lu Q, Mi N, Li H, Liu M, Xu M, Tan L, Xie Q, Zhang Y, Yao S. Electrochemical synthesis of carbon nanodots directly from alcohols. Chemistry. 2014 Apr 22;20(17):4993-9. doi: 10.1002/chem.201304869. Epub 2014 Mar 12. PMID: 24623706.
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First practical cross-alkylation of primary alcohols with a new and recyclable impregnated iridium on magnetite catalyst.

Chemical communications (Cambridge, England)

Cano R, Yus M, Ramón DJ.
PMID: 22732869
Chem Commun (Camb). 2012 Aug 07;48(61):7628-30. doi: 10.1039/c2cc33101b. Epub 2012 Jun 26.

A new impregnated iridium on magnetite catalyst has been prepared, characterized, used and recycled, up to ten times with practically the same activity, for the first practical cross-alkylation of primary alcohols. The catalyst showed a wide reaction scope, is...

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Cano R, Yus M, Ramón DJ. First practical cross-alkylation of primary alcohols with a new and recyclable impregnated iridium on magnetite catalyst. Chem Commun (Camb). 2012;48(61):7628-30doi: 10.1039/c2cc33101b.
Cano, R., Yus, M., & Ramón, D. J. (2012). First practical cross-alkylation of primary alcohols with a new and recyclable impregnated iridium on magnetite catalyst. Chemical communications (Cambridge, England), 48(61), 7628-30. https://doi.org/10.1039/c2cc33101b
Cano, Rafael, et al. "First practical cross-alkylation of primary alcohols with a new and recyclable impregnated iridium on magnetite catalyst." Chemical communications (Cambridge, England) vol. 48,61 (2012): 7628-30. doi: https://doi.org/10.1039/c2cc33101b
Cano R, Yus M, Ramón DJ. First practical cross-alkylation of primary alcohols with a new and recyclable impregnated iridium on magnetite catalyst. Chem Commun (Camb). 2012 Aug 07;48(61):7628-30. doi: 10.1039/c2cc33101b. Epub 2012 Jun 26. PMID: 22732869.
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Cloning and characterization of Pfl_1841, a 2-methylenebornane synthase in Pseudomonas fluorescens PfO-1.

Tetrahedron

Chou WK, Ikeda H, Cane DE.
PMID: 21804650
Tetrahedron. 2011 Sep 02;67(35):6627-6632. doi: 10.1016/j.tet.2011.05.084.

The pfl_1841 gene from Pseudomonas fluorescens PfO-1 is the only gene in any of the three sequenced genomes of the Gram-negative bacterium Pseudomonas fluorescens that is annotated as a putative terpene synthase. The predicted Pfl_1841 protein, which harbors the...

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Chou WK, Ikeda H, Cane DE. Cloning and characterization of Pfl_1841, a 2-methylenebornane synthase in Pseudomonas fluorescens PfO-1. Tetrahedron. 2011;67(35):6627-6632doi: 10.1016/j.tet.2011.05.084.
Chou, W. K., Ikeda, H., & Cane, D. E. (2011). Cloning and characterization of Pfl_1841, a 2-methylenebornane synthase in Pseudomonas fluorescens PfO-1. Tetrahedron, 67(35), 6627-6632. https://doi.org/10.1016/j.tet.2011.05.084
Chou, Wayne K W, et al. "Cloning and characterization of Pfl_1841, a 2-methylenebornane synthase in Pseudomonas fluorescens PfO-1." Tetrahedron vol. 67,35 (2011): 6627-6632. doi: https://doi.org/10.1016/j.tet.2011.05.084
Chou WK, Ikeda H, Cane DE. Cloning and characterization of Pfl_1841, a 2-methylenebornane synthase in Pseudomonas fluorescens PfO-1. Tetrahedron. 2011 Sep 02;67(35):6627-6632. doi: 10.1016/j.tet.2011.05.084. PMID: 21804650; PMCID: PMC3144570.
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Reaction-based and single fluorescent emitter decorated ratiometric nanoprobe to detect hydrogen peroxide.

Chemistry (Weinheim an der Bergstrasse, Germany)

Chen CY, Chen CT.
PMID: 24123627
Chemistry. 2013 Nov 18;19(47):16050-7. doi: 10.1002/chem.201302342. Epub 2013 Oct 10.

A novel reaction-based cross-linked polymeric nanoprobe with a self-calibrating ratiometric fluorescence readout to selectively detect H2O2 is reported. The polymeric nanoprobe is fabricated by using hydrophobic H2O2-reactive boronic ester groups, crosslinker units, and environmentally sensitive 3-hydroxyflavone fluorophores through a...

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Chen CY, Chen CT. Reaction-based and single fluorescent emitter decorated ratiometric nanoprobe to detect hydrogen peroxide. Chemistry. 2013;19(47):16050-7doi: 10.1002/chem.201302342.
Chen, C. Y., & Chen, C. T. (2013). Reaction-based and single fluorescent emitter decorated ratiometric nanoprobe to detect hydrogen peroxide. Chemistry (Weinheim an der Bergstrasse, Germany), 19(47), 16050-7. https://doi.org/10.1002/chem.201302342
Chen, Chun-Yen, and Chen, Chao-Tsen. "Reaction-based and single fluorescent emitter decorated ratiometric nanoprobe to detect hydrogen peroxide." Chemistry (Weinheim an der Bergstrasse, Germany) vol. 19,47 (2013): 16050-7. doi: https://doi.org/10.1002/chem.201302342
Chen CY, Chen CT. Reaction-based and single fluorescent emitter decorated ratiometric nanoprobe to detect hydrogen peroxide. Chemistry. 2013 Nov 18;19(47):16050-7. doi: 10.1002/chem.201302342. Epub 2013 Oct 10. PMID: 24123627.
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Gold(I)-catalyzed synthesis of γ-vinylbutyrolactones by intramolecular oxaallylic alkylation with alcohols.

Beilstein journal of organic chemistry

Chiarucci M, Locritani M, Cera G, Bandini M.
PMID: 21977203
Beilstein J Org Chem. 2011;7:1198-204. doi: 10.3762/bjoc.7.139. Epub 2011 Sep 01.

Gold(I)-N-heterocyclic carbene (NHC) complexes proved to be a reliable catalytic system for the direct synthesis of functionalized γ-vinylbutyrolactones by intramolecular oxaallylic alkylation with primary alcohols. Good isolated chemical yields were obtained for a range of malonyl and acetate derivatives....

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Chiarucci M, Locritani M, Cera G, et al. Gold(I)-catalyzed synthesis of γ-vinylbutyrolactones by intramolecular oxaallylic alkylation with alcohols. Beilstein J Org Chem. 2011;7:1198-204doi: 10.3762/bjoc.7.139.
Chiarucci, M., Locritani, M., Cera, G., & Bandini, M. (2011). Gold(I)-catalyzed synthesis of γ-vinylbutyrolactones by intramolecular oxaallylic alkylation with alcohols. Beilstein journal of organic chemistry, 71198-204. https://doi.org/10.3762/bjoc.7.139
Chiarucci, Michel, et al. "Gold(I)-catalyzed synthesis of γ-vinylbutyrolactones by intramolecular oxaallylic alkylation with alcohols." Beilstein journal of organic chemistry vol. 7 (2011): 1198-204. doi: https://doi.org/10.3762/bjoc.7.139
Chiarucci M, Locritani M, Cera G, Bandini M. Gold(I)-catalyzed synthesis of γ-vinylbutyrolactones by intramolecular oxaallylic alkylation with alcohols. Beilstein J Org Chem. 2011;7:1198-204. doi: 10.3762/bjoc.7.139. Epub 2011 Sep 01. PMID: 21977203; PMCID: PMC3182428.
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Convenient photooxidation of alcohols using dye sensitised semiconductors in combination with silver nitrate and TEMPO--an electron paramagnetic resonance study.

Dalton transactions (Cambridge, England : 2003)

Jeena V, Robinson RS.
PMID: 22278171
Dalton Trans. 2012 Mar 21;41(11):3134-7. doi: 10.1039/c2dt12030e. Epub 2012 Jan 25.

A mechanistic investigation into the photooxidation of alcohols using dye sensitised titanium dioxide and dye sensitised zinc oxide is described. The varying yields using the two photocatalysts have been explained using electron paramagnetic resonance (EPR) spectroscopy, which indicated that...

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Jeena V, Robinson RS. Convenient photooxidation of alcohols using dye sensitised semiconductors in combination with silver nitrate and TEMPO--an electron paramagnetic resonance study. Dalton Trans. 2012;41(11):3134-7doi: 10.1039/c2dt12030e.
Jeena, V., & Robinson, R. S. (2012). Convenient photooxidation of alcohols using dye sensitised semiconductors in combination with silver nitrate and TEMPO--an electron paramagnetic resonance study. Dalton transactions (Cambridge, England : 2003), 41(11), 3134-7. https://doi.org/10.1039/c2dt12030e
Jeena, Vineet, and Robinson, Ross S. "Convenient photooxidation of alcohols using dye sensitised semiconductors in combination with silver nitrate and TEMPO--an electron paramagnetic resonance study." Dalton transactions (Cambridge, England : 2003) vol. 41,11 (2012): 3134-7. doi: https://doi.org/10.1039/c2dt12030e
Jeena V, Robinson RS. Convenient photooxidation of alcohols using dye sensitised semiconductors in combination with silver nitrate and TEMPO--an electron paramagnetic resonance study. Dalton Trans. 2012 Mar 21;41(11):3134-7. doi: 10.1039/c2dt12030e. Epub 2012 Jan 25. PMID: 22278171.
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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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Assessing the chemotaxis behavior of Physarum polycephalum to a range of simple volatile organic chemicals.

Communicative & integrative biology

de Lacy Costello BP, Adamatzky AI.
PMID: 24265848
Commun Integr Biol. 2013 Sep 01;6(5):e25030. doi: 10.4161/cib.25030. Epub 2013 Jun 14.

The chemotaxis behavior of the plasmodial stage of the true slime mold Physarum Polycephalum was assessed when given a binary choice between two volatile organic chemicals (VOCs) placed in its environment. All possible binary combinations were tested between 19...

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de Lacy Costello BP, Adamatzky AI. Assessing the chemotaxis behavior of Physarum polycephalum to a range of simple volatile organic chemicals. Commun Integr Biol. 2013;6(5):e25030doi: 10.4161/cib.25030.
de Lacy Costello, B. P., & Adamatzky, A. I. (2013). Assessing the chemotaxis behavior of Physarum polycephalum to a range of simple volatile organic chemicals. Communicative & integrative biology, 6(5), e25030. https://doi.org/10.4161/cib.25030
de Lacy Costello, Ben P J, and Adamatzky, Andrew I. "Assessing the chemotaxis behavior of Physarum polycephalum to a range of simple volatile organic chemicals." Communicative & integrative biology vol. 6,5 (2013): e25030. doi: https://doi.org/10.4161/cib.25030
de Lacy Costello BP, Adamatzky AI. Assessing the chemotaxis behavior of Physarum polycephalum to a range of simple volatile organic chemicals. Commun Integr Biol. 2013 Sep 01;6(5):e25030. doi: 10.4161/cib.25030. Epub 2013 Jun 14. PMID: 24265848; PMCID: PMC3829954.
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Towards a rapid near-infrared technique for prediction of resistance to sugarcane borerEldana saccharina walker (Lepidoptera: Pyralidae) using stalk surface wax.

Journal of chemical ecology

Rutherford RS, van Staden J.
PMID: 24227577
J Chem Ecol. 1996 Apr;22(4):681-94. doi: 10.1007/BF02033578.

Multiple regression predictive models based on data acquired by near-infrared (NIR) spectrophotometry suggest that stalk surface wax components contribute towards resistance toEldana saccharina Walker in sugarcane. At least 35 sugarcane clones of known resistance were required to calibrate a...

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Rutherford RS, van Staden J. Towards a rapid near-infrared technique for prediction of resistance to sugarcane borerEldana saccharina walker (Lepidoptera: Pyralidae) using stalk surface wax. J Chem Ecol. 1996;22(4):681-94doi: 10.1007/BF02033578.
Rutherford, R. S., & van Staden, J. (1996). Towards a rapid near-infrared technique for prediction of resistance to sugarcane borerEldana saccharina walker (Lepidoptera: Pyralidae) using stalk surface wax. Journal of chemical ecology, 22(4), 681-94. https://doi.org/10.1007/BF02033578
Rutherford, R S, and van Staden, J. "Towards a rapid near-infrared technique for prediction of resistance to sugarcane borerEldana saccharina walker (Lepidoptera: Pyralidae) using stalk surface wax." Journal of chemical ecology vol. 22,4 (1996): 681-94. doi: https://doi.org/10.1007/BF02033578
Rutherford RS, van Staden J. Towards a rapid near-infrared technique for prediction of resistance to sugarcane borerEldana saccharina walker (Lepidoptera: Pyralidae) using stalk surface wax. J Chem Ecol. 1996 Apr;22(4):681-94. doi: 10.1007/BF02033578. PMID: 24227577.
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Mammalian exocrine secretions: X. constituents of preorbital secretion of grysbok,Raphicerus melanotis.

Journal of chemical ecology

Burger BV, Tien FC, Le Roux M, Mo WP.
PMID: 24227582
J Chem Ecol. 1996 Apr;22(4):739-64. doi: 10.1007/BF02033583.

Using electron impact and chemical ionization mass spectrometry with methane and nitric oxide as reactant gases in conjunction with mass spectral analysis of the dimethyl disulfide derivatives of unsaturated constituents, 51 compounds have been identified in addition to the...

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Burger BV, Tien FC, Le Roux M, et al. Mammalian exocrine secretions: X. constituents of preorbital secretion of grysbok,Raphicerus melanotis. J Chem Ecol. 1996;22(4):739-64doi: 10.1007/BF02033583.
Burger, B. V., Tien, F. C., Le Roux, M., & Mo, W. P. (1996). Mammalian exocrine secretions: X. constituents of preorbital secretion of grysbok,Raphicerus melanotis. Journal of chemical ecology, 22(4), 739-64. https://doi.org/10.1007/BF02033583
Burger, B V, et al. "Mammalian exocrine secretions: X. constituents of preorbital secretion of grysbok,Raphicerus melanotis." Journal of chemical ecology vol. 22,4 (1996): 739-64. doi: https://doi.org/10.1007/BF02033583
Burger BV, Tien FC, Le Roux M, Mo WP. Mammalian exocrine secretions: X. constituents of preorbital secretion of grysbok,Raphicerus melanotis. J Chem Ecol. 1996 Apr;22(4):739-64. doi: 10.1007/BF02033583. PMID: 24227582.
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Novel carbocationic rearrangements of 1-styrylpropargyl alcohols.

Beilstein journal of organic chemistry

Basmadjian C, Zhang F, Désaubry L.
PMID: 26199656
Beilstein J Org Chem. 2015 Jun 15;11:1017-22. doi: 10.3762/bjoc.11.114. eCollection 2015.

The dehydration and subsequent cyclization reactions of 1-styrylpropargyl alcohols was examined. In the course of these studies, numerous scaffolds were synthesized, including a furan, a cyclopentenone, an acyclic enone and even a naphthalenone. The diversity of these structural motifs...

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Basmadjian C, Zhang F, Désaubry L. Novel carbocationic rearrangements of 1-styrylpropargyl alcohols. Beilstein J Org Chem. 2015;11:1017-22doi: 10.3762/bjoc.11.114.
Basmadjian, C., Zhang, F., & Désaubry, L. (2015). Novel carbocationic rearrangements of 1-styrylpropargyl alcohols. Beilstein journal of organic chemistry, 111017-22. https://doi.org/10.3762/bjoc.11.114
Basmadjian, Christine, et al. "Novel carbocationic rearrangements of 1-styrylpropargyl alcohols." Beilstein journal of organic chemistry vol. 11 (2015): 1017-22. doi: https://doi.org/10.3762/bjoc.11.114
Basmadjian C, Zhang F, Désaubry L. Novel carbocationic rearrangements of 1-styrylpropargyl alcohols. Beilstein J Org Chem. 2015 Jun 15;11:1017-22. doi: 10.3762/bjoc.11.114. eCollection 2015. PMID: 26199656; PMCID: PMC4505300.
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Showing 1 to 12 of 9631 entries