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The Ketogenic Diet Revisited: Beyond Ketones.

Frontiers in neurology

Sourbron J, Thevissen K, Lagae L.
PMID: 34393987
Front Neurol. 2021 Jul 30;12:720073. doi: 10.3389/fneur.2021.720073. eCollection 2021.

No abstract available.

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Sourbron J, Thevissen K, Lagae L. The Ketogenic Diet Revisited: Beyond Ketones. Front Neurol. 2021;12:720073doi: 10.3389/fneur.2021.720073.
Sourbron, J., Thevissen, K., & Lagae, L. (2021). The Ketogenic Diet Revisited: Beyond Ketones. Frontiers in neurology, 12720073. https://doi.org/10.3389/fneur.2021.720073
Sourbron, Jo, et al. "The Ketogenic Diet Revisited: Beyond Ketones." Frontiers in neurology vol. 12 (2021): 720073. doi: https://doi.org/10.3389/fneur.2021.720073
Sourbron J, Thevissen K, Lagae L. The Ketogenic Diet Revisited: Beyond Ketones. Front Neurol. 2021 Jul 30;12:720073. doi: 10.3389/fneur.2021.720073. eCollection 2021. PMID: 34393987; PMCID: PMC8363000.
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Enantioselective γ-Addition-Driven Cascade of β,γ-Unsaturated Ketones by Ion-Pair Catalysis: Access to Chiral 1,3-Dioxolochroman Scaffolds.

Organic letters

Wang X, Zhou L, Zhang H, Ren X, Gao G, Wang T.
PMID: 34932357
Org Lett. 2022 Jan 14;24(1):38-42. doi: 10.1021/acs.orglett.1c03567. Epub 2021 Dec 21.

A highly enantioselective γ-addition-driven cascade of β,γ-unsaturated carbonyl compounds by bifunctional ion-pair catalysis has been developed. With this protocol, a range of functionalized chiral 1,3-dioxolochroman derivatives were prepared in high yields with superior stereoselectivities (>99%

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Wang X, Zhou L, Zhang H, et al. Enantioselective γ-Addition-Driven Cascade of β,γ-Unsaturated Ketones by Ion-Pair Catalysis: Access to Chiral 1,3-Dioxolochroman Scaffolds. Org Lett. 2021;24(1):38-42doi: 10.1021/acs.orglett.1c03567.
Wang, X., Zhou, L., Zhang, H., Ren, X., Gao, G., & Wang, T. (2022). Enantioselective γ-Addition-Driven Cascade of β,γ-Unsaturated Ketones by Ion-Pair Catalysis: Access to Chiral 1,3-Dioxolochroman Scaffolds. Organic letters, 24(1), 38-42. https://doi.org/10.1021/acs.orglett.1c03567
Wang, Xuemei, et al. "Enantioselective γ-Addition-Driven Cascade of β,γ-Unsaturated Ketones by Ion-Pair Catalysis: Access to Chiral 1,3-Dioxolochroman Scaffolds." Organic letters vol. 24,1 (2022): 38-42. doi: https://doi.org/10.1021/acs.orglett.1c03567
Wang X, Zhou L, Zhang H, Ren X, Gao G, Wang T. Enantioselective γ-Addition-Driven Cascade of β,γ-Unsaturated Ketones by Ion-Pair Catalysis: Access to Chiral 1,3-Dioxolochroman Scaffolds. Org Lett. 2022 Jan 14;24(1):38-42. doi: 10.1021/acs.orglett.1c03567. Epub 2021 Dec 21. PMID: 34932357.
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Bioengineering human placentas: social implications of an advancing field.

Trends in biotechnology

Dalziell J, Keaney J, Kearnes M, Thierry B, Winter M.
PMID: 34844773
Trends Biotechnol. 2022 Feb;40(2):137-140. doi: 10.1016/j.tibtech.2021.10.011. Epub 2021 Nov 26.

Technological advances in bioengineering, especially in microphysiological systems and organoids, are changing the way in which placental tissue is used and perceived. These advances raise important questions surrounding consent, privacy, biobanking, and research ethics. We explore emerging technologies which...

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Dalziell J, Keaney J, Kearnes M, et al. Bioengineering human placentas: social implications of an advancing field. Trends Biotechnol. 2021;40(2):137-140doi: 10.1016/j.tibtech.2021.10.011.
Dalziell, J., Keaney, J., Kearnes, M., Thierry, B., & Winter, M. (2022). Bioengineering human placentas: social implications of an advancing field. Trends in biotechnology, 40(2), 137-140. https://doi.org/10.1016/j.tibtech.2021.10.011
Dalziell, Jacqueline, et al. "Bioengineering human placentas: social implications of an advancing field." Trends in biotechnology vol. 40,2 (2022): 137-140. doi: https://doi.org/10.1016/j.tibtech.2021.10.011
Dalziell J, Keaney J, Kearnes M, Thierry B, Winter M. Bioengineering human placentas: social implications of an advancing field. Trends Biotechnol. 2022 Feb;40(2):137-140. doi: 10.1016/j.tibtech.2021.10.011. Epub 2021 Nov 26. PMID: 34844773.
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α- and β-Functionalized Ketones from 1,3-Dienes and Aldehydes: Control of Regio- and Enantioselectivity in Hydroacylation of 1,3-Dienes.

Journal of the American Chemical Society

Parsutkar MM, RajanBabu TV.
PMID: 34351138
J Am Chem Soc. 2021 Aug 18;143(32):12825-12835. doi: 10.1021/jacs.1c06245. Epub 2021 Aug 05.

Ketones are among the most widely used intermediates in organic synthesis, and their synthesis from inexpensive feedstocks could be quite impactful. Regio- and enantioselective hydroacylation reactions of dienes provide facile entry into useful ketone-bearing chiral motifs with an additional...

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Parsutkar MM, RajanBabu TV. α- and β-Functionalized Ketones from 1,3-Dienes and Aldehydes: Control of Regio- and Enantioselectivity in Hydroacylation of 1,3-Dienes. J Am Chem Soc. 2021;143(32):12825-12835doi: 10.1021/jacs.1c06245.
Parsutkar, M. M., & RajanBabu, T. V. (2021). α- and β-Functionalized Ketones from 1,3-Dienes and Aldehydes: Control of Regio- and Enantioselectivity in Hydroacylation of 1,3-Dienes. Journal of the American Chemical Society, 143(32), 12825-12835. https://doi.org/10.1021/jacs.1c06245
Parsutkar, Mahesh M, and RajanBabu, T V. "α- and β-Functionalized Ketones from 1,3-Dienes and Aldehydes: Control of Regio- and Enantioselectivity in Hydroacylation of 1,3-Dienes." Journal of the American Chemical Society vol. 143,32 (2021): 12825-12835. doi: https://doi.org/10.1021/jacs.1c06245
Parsutkar MM, RajanBabu TV. α- and β-Functionalized Ketones from 1,3-Dienes and Aldehydes: Control of Regio- and Enantioselectivity in Hydroacylation of 1,3-Dienes. J Am Chem Soc. 2021 Aug 18;143(32):12825-12835. doi: 10.1021/jacs.1c06245. Epub 2021 Aug 05. PMID: 34351138; PMCID: PMC8554466.
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IRES: International Chemistry Research Experience for Students in Vietnam.

[No authors listed]
UIID-NSF: 984

OISE-0744375 (Pratt, L.M. - Fisk University) IRES: International Chemistry Research Experience for Students in Vietnam Over a three-year period this International Research Experience for Students (IRES) project will annually provide nine U.S. undergraduate and graduate students with a nine-week...

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IRES: International Chemistry Research Experience for Students in Vietnam. ;
(). IRES: International Chemistry Research Experience for Students in Vietnam. .
"IRES: International Chemistry Research Experience for Students in Vietnam." vol. ().
IRES: International Chemistry Research Experience for Students in Vietnam. UIID-NSF: 984.
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Showing 6637 to 6641 of 6641 entries