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Showing 1 to 9 of 9 entries
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Organic chemistry: A cure for catalyst poisoning.

Nature

Farmer ME, Baran PS.
PMID: 26268186
Nature. 2015 Aug 13;524(7564):164-5. doi: 10.1038/524164a.

No abstract available.

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Farmer ME, Baran PS. Organic chemistry: A cure for catalyst poisoning. Nature. 2015;524(7564):164-5doi: 10.1038/524164a.
Farmer, M. E., & Baran, P. S. (2015). Organic chemistry: A cure for catalyst poisoning. Nature, 524(7564), 164-5. https://doi.org/10.1038/524164a
Farmer, Marcus E, and Baran, Phil S. "Organic chemistry: A cure for catalyst poisoning." Nature vol. 524,7564 (2015): 164-5. doi: https://doi.org/10.1038/524164a
Farmer ME, Baran PS. Organic chemistry: A cure for catalyst poisoning. Nature. 2015 Aug 13;524(7564):164-5. doi: 10.1038/524164a. PMID: 26268186.
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Pattern transformation with DNA circuits.

Nature chemistry

Chirieleison SM, Allen PB, Simpson ZB, Ellington AD, Chen X.
PMID: 24256862
Nat Chem. 2013 Dec;5(12):1000-5. doi: 10.1038/nchem.1764. Epub 2013 Sep 29.

Readily programmable chemical networks are important tools as the scope of chemistry expands from individual molecules to larger molecular systems. Although many complex systems are constructed using conventional organic and inorganic chemistry, the programmability of biological molecules such as...

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Chirieleison SM, Allen PB, Simpson ZB, et al. Pattern transformation with DNA circuits. Nat Chem. 2013;5(12):1000-5doi: 10.1038/nchem.1764.
Chirieleison, S. M., Allen, P. B., Simpson, Z. B., Ellington, A. D., & Chen, X. (2013). Pattern transformation with DNA circuits. Nature chemistry, 5(12), 1000-5. https://doi.org/10.1038/nchem.1764
Chirieleison, Steven M, et al. "Pattern transformation with DNA circuits." Nature chemistry vol. 5,12 (2013): 1000-5. doi: https://doi.org/10.1038/nchem.1764
Chirieleison SM, Allen PB, Simpson ZB, Ellington AD, Chen X. Pattern transformation with DNA circuits. Nat Chem. 2013 Dec;5(12):1000-5. doi: 10.1038/nchem.1764. Epub 2013 Sep 29. PMID: 24256862; PMCID: PMC3970425.
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Parallel lines.

Nature

[No authors listed]
PMID: 24579098
Nature. 2014 Feb 27;506(7489):407-8. doi: 10.1038/506407b.

No abstract available.

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Parallel lines. Nature. 2014;506(7489):407-8doi: 10.1038/506407b.
(2014). Parallel lines. Nature, 506(7489), 407-8. https://doi.org/10.1038/506407b
"Parallel lines." Nature vol. 506,7489 (2014): 407-8. doi: https://doi.org/10.1038/506407b
Parallel lines. Nature. 2014 Feb 27;506(7489):407-8. doi: 10.1038/506407b. PMID: 24579098.
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Novel Methodologies for Chemical Activation in Organic Synthesis under Solvent-Free Reaction Conditions.

Molecules (Basel, Switzerland)

Avila-Ortiz CG, Juaristi E.
PMID: 32781678
Molecules. 2020 Aug 06;25(16). doi: 10.3390/molecules25163579.

One central challenge for XXI century chemists is the development of sustainable processes that do not represent a risk either to humanity or to the environment. In this regard, the search for more efficient and clean alternatives to achieve...

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Avila-Ortiz CG, Juaristi E. Novel Methodologies for Chemical Activation in Organic Synthesis under Solvent-Free Reaction Conditions. Molecules. 2020;25(16)doi: 10.3390/molecules25163579.
Avila-Ortiz, C. G., & Juaristi, E. (2020). Novel Methodologies for Chemical Activation in Organic Synthesis under Solvent-Free Reaction Conditions. Molecules (Basel, Switzerland), 25(16), . https://doi.org/10.3390/molecules25163579
Avila-Ortiz, Claudia Gabriela, and Juaristi, Eusebio. "Novel Methodologies for Chemical Activation in Organic Synthesis under Solvent-Free Reaction Conditions." Molecules (Basel, Switzerland) vol. 25,16 (2020). doi: https://doi.org/10.3390/molecules25163579
Avila-Ortiz CG, Juaristi E. Novel Methodologies for Chemical Activation in Organic Synthesis under Solvent-Free Reaction Conditions. Molecules. 2020 Aug 06;25(16). doi: 10.3390/molecules25163579. PMID: 32781678; PMCID: PMC7464687.
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Editorial.

Bioconjugate chemistry

van Hest J, Lavik EB, Smith BD, Zheng G, Rotello VM.
PMID: 25588645
Bioconjug Chem. 2015 Feb 18;26(2):163-5. doi: 10.1021/acs.bioconjchem.5b00002. Epub 2015 Jan 15.

No abstract available.

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van Hest J, Lavik EB, Smith BD, et al. Editorial. Bioconjug Chem. 2015;26(2):163-5doi: 10.1021/acs.bioconjchem.5b00002.
van Hest, J., Lavik, E. B., Smith, B. D., Zheng, G., & Rotello, V. M. (2015). Editorial. Bioconjugate chemistry, 26(2), 163-5. https://doi.org/10.1021/acs.bioconjchem.5b00002
van Hest, Jan, et al. "Editorial." Bioconjugate chemistry vol. 26,2 (2015): 163-5. doi: https://doi.org/10.1021/acs.bioconjchem.5b00002
van Hest J, Lavik EB, Smith BD, Zheng G, Rotello VM. Editorial. Bioconjug Chem. 2015 Feb 18;26(2):163-5. doi: 10.1021/acs.bioconjchem.5b00002. Epub 2015 Jan 15. PMID: 25588645.
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Next generation diversity-oriented synthesis: a paradigm shift from chemical diversity to biological diversity.

Organic & biomolecular chemistry

Pavlinov I, Gerlach EM, Aldrich LN.
PMID: 30328455
Org Biomol Chem. 2019 Feb 13;17(7):1608-1623. doi: 10.1039/c8ob02327a.

Diversity-oriented synthesis has historically focused on the generation of small-molecule collections with considerable scaffold, stereochemical, and appendage diversity. Recently, this focus has begun to shift to the production of small-molecule libraries with diverse biological activities. It is currently not...

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Pavlinov I, Gerlach EM, Aldrich LN. Next generation diversity-oriented synthesis: a paradigm shift from chemical diversity to biological diversity. Org Biomol Chem. 2019;17(7):1608-1623doi: 10.1039/c8ob02327a.
Pavlinov, I., Gerlach, E. M., & Aldrich, L. N. (2019). Next generation diversity-oriented synthesis: a paradigm shift from chemical diversity to biological diversity. Organic & biomolecular chemistry, 17(7), 1608-1623. https://doi.org/10.1039/c8ob02327a
Pavlinov, Ivan, et al. "Next generation diversity-oriented synthesis: a paradigm shift from chemical diversity to biological diversity." Organic & biomolecular chemistry vol. 17,7 (2019): 1608-1623. doi: https://doi.org/10.1039/c8ob02327a
Pavlinov I, Gerlach EM, Aldrich LN. Next generation diversity-oriented synthesis: a paradigm shift from chemical diversity to biological diversity. Org Biomol Chem. 2019 Feb 13;17(7):1608-1623. doi: 10.1039/c8ob02327a. PMID: 30328455.
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Predicting Retrosynthetic Reactions Using Self-Corrected Transformer Neural Networks.

Journal of chemical information and modeling

Zheng S, Rao J, Zhang Z, Xu J, Yang Y.
PMID: 31825611
J Chem Inf Model. 2020 Jan 27;60(1):47-55. doi: 10.1021/acs.jcim.9b00949. Epub 2019 Dec 24.

Synthesis planning is the process of recursively decomposing target molecules into available precursors. Computer-aided retrosynthesis can potentially assist chemists in designing synthetic routes; however, at present, it is cumbersome and cannot provide satisfactory results. In this study, we have...

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Zheng S, Rao J, Zhang Z, et al. Predicting Retrosynthetic Reactions Using Self-Corrected Transformer Neural Networks. J Chem Inf Model. 2019;60(1):47-55doi: 10.1021/acs.jcim.9b00949.
Zheng, S., Rao, J., Zhang, Z., Xu, J., & Yang, Y. (2020). Predicting Retrosynthetic Reactions Using Self-Corrected Transformer Neural Networks. Journal of chemical information and modeling, 60(1), 47-55. https://doi.org/10.1021/acs.jcim.9b00949
Zheng, Shuangjia, et al. "Predicting Retrosynthetic Reactions Using Self-Corrected Transformer Neural Networks." Journal of chemical information and modeling vol. 60,1 (2020): 47-55. doi: https://doi.org/10.1021/acs.jcim.9b00949
Zheng S, Rao J, Zhang Z, Xu J, Yang Y. Predicting Retrosynthetic Reactions Using Self-Corrected Transformer Neural Networks. J Chem Inf Model. 2020 Jan 27;60(1):47-55. doi: 10.1021/acs.jcim.9b00949. Epub 2019 Dec 24. PMID: 31825611.
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High-throughput development of amphiphile self-assembly materials: fast-tracking synthesis, characterization, formulation, application, and understanding.

Accounts of chemical research

Mulet X, Conn CE, Fong C, Kennedy DF, Moghaddam MJ, Drummond CJ.
PMID: 23427836
Acc Chem Res. 2013 Jul 16;46(7):1497-505. doi: 10.1021/ar300285u. Epub 2013 Feb 21.

Amphiphile self-assembly materials, which contain both a hydrophilic and a hydrophobic domain, have great potential in high-throughput and combinatorial approaches to discovery and development. However, the materials chemistry community has not embraced these ideas to anywhere near the extent...

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Mulet X, Conn CE, Fong C, et al. High-throughput development of amphiphile self-assembly materials: fast-tracking synthesis, characterization, formulation, application, and understanding. Acc Chem Res. 2013;46(7):1497-505doi: 10.1021/ar300285u.
Mulet, X., Conn, C. E., Fong, C., Kennedy, D. F., Moghaddam, M. J., & Drummond, C. J. (2013). High-throughput development of amphiphile self-assembly materials: fast-tracking synthesis, characterization, formulation, application, and understanding. Accounts of chemical research, 46(7), 1497-505. https://doi.org/10.1021/ar300285u
Mulet, Xavier, et al. "High-throughput development of amphiphile self-assembly materials: fast-tracking synthesis, characterization, formulation, application, and understanding." Accounts of chemical research vol. 46,7 (2013): 1497-505. doi: https://doi.org/10.1021/ar300285u
Mulet X, Conn CE, Fong C, Kennedy DF, Moghaddam MJ, Drummond CJ. High-throughput development of amphiphile self-assembly materials: fast-tracking synthesis, characterization, formulation, application, and understanding. Acc Chem Res. 2013 Jul 16;46(7):1497-505. doi: 10.1021/ar300285u. Epub 2013 Feb 21. PMID: 23427836.
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Deep eutectic solvents in polymerizations: a greener alternative to conventional syntheses.

ChemSusChem

del Monte F, Carriazo D, Serrano MC, Gutiérrez MC, Ferrer ML.
PMID: 24376090
ChemSusChem. 2014 Apr;7(4):999-1009. doi: 10.1002/cssc.201300864. Epub 2013 Dec 27.

The use of deep eutectic solvents (DESs) that act as all-in-one solvent-template-reactant systems offers an interesting green alternative to conventional syntheses in materials science. This Review aims to provide a comprehensive overview to emphasize the similarities and discrepancies between...

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del Monte F, Carriazo D, Serrano MC, et al. Deep eutectic solvents in polymerizations: a greener alternative to conventional syntheses. ChemSusChem. 2013;7(4):999-1009doi: 10.1002/cssc.201300864.
del Monte, F., Carriazo, D., Serrano, M. C., Gutiérrez, M. C., & Ferrer, M. L. (2014). Deep eutectic solvents in polymerizations: a greener alternative to conventional syntheses. ChemSusChem, 7(4), 999-1009. https://doi.org/10.1002/cssc.201300864
del Monte, Francisco, et al. "Deep eutectic solvents in polymerizations: a greener alternative to conventional syntheses." ChemSusChem vol. 7,4 (2014): 999-1009. doi: https://doi.org/10.1002/cssc.201300864
del Monte F, Carriazo D, Serrano MC, Gutiérrez MC, Ferrer ML. Deep eutectic solvents in polymerizations: a greener alternative to conventional syntheses. ChemSusChem. 2014 Apr;7(4):999-1009. doi: 10.1002/cssc.201300864. Epub 2013 Dec 27. PMID: 24376090.
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Showing 1 to 9 of 9 entries