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Phytochemical composition, antiparasitic and α-glucosidase inhibition activities from .

Chemistry Central journal

López D, Cherigo L, Spadafora C, Loza-Mejía MA, Martínez-Luis S.
PMID: 26435737
Chem Cent J. 2015 Sep 28;9(1):53. doi: 10.1186/s13065-015-0130-3. eCollection 2015 Dec.

BACKGROUND: Panama has an extensive mangrove area and it is one of the countries with the highest biodiversity in America. Mangroves are widely used in traditional medicine, nevertheless, there are very few studies that validates their medicinal properties in...

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López D, Cherigo L, Spadafora C, et al. Phytochemical composition, antiparasitic and α-glucosidase inhibition activities from . Chem Cent J. 2015;9(1):53doi: 10.1186/s13065-015-0130-3.
López, D., Cherigo, L., Spadafora, C., Loza-Mejía, M. A., & Martínez-Luis, S. (2015). Phytochemical composition, antiparasitic and α-glucosidase inhibition activities from . Chemistry Central journal, 9(1), 53. https://doi.org/10.1186/s13065-015-0130-3
López, Dioxelis, et al. "Phytochemical composition, antiparasitic and α-glucosidase inhibition activities from ." Chemistry Central journal vol. 9,1 (2015): 53. doi: https://doi.org/10.1186/s13065-015-0130-3
López D, Cherigo L, Spadafora C, Loza-Mejía MA, Martínez-Luis S. Phytochemical composition, antiparasitic and α-glucosidase inhibition activities from . Chem Cent J. 2015 Sep 28;9(1):53. doi: 10.1186/s13065-015-0130-3. eCollection 2015 Dec. PMID: 26435737; PMCID: PMC4586009.
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Formal gas-phase polar [4 + 1+] cycloaddition of ionized methylene to alpha-dicarbonyl compounds: synthesis of 2-unsubstituted 1,3-dioxoles.

Journal of mass spectrometry : JMS

Meurer EC, Cabrini LG, Gozzo FC, Eberlin MN.
PMID: 16604574
J Mass Spectrom. 2006 Jun;41(6):735-40. doi: 10.1002/jms.1029.

Ion/molecule reactions of +CH2OCH2. with alpha-dicarbonyl compounds were performed via pentaquadrupole mass spectrometry. Besides the previously known [3+ + 2] 1,3-cycloaddition reaction that forms cyclic 1,3-dioxonium ions, an unprecedented reaction proceeding formally by [4 + 1+] cycloaddition of ionized...

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Meurer EC, Cabrini LG, Gozzo FC, et al. Formal gas-phase polar [4 + 1+] cycloaddition of ionized methylene to alpha-dicarbonyl compounds: synthesis of 2-unsubstituted 1,3-dioxoles. J Mass Spectrom. 2006;41(6):735-40doi: 10.1002/jms.1029.
Meurer, E. C., Cabrini, L. G., Gozzo, F. C., & Eberlin, M. N. (2006). Formal gas-phase polar [4 + 1+] cycloaddition of ionized methylene to alpha-dicarbonyl compounds: synthesis of 2-unsubstituted 1,3-dioxoles. Journal of mass spectrometry : JMS, 41(6), 735-40. https://doi.org/10.1002/jms.1029
Meurer, Eduardo C, et al. "Formal gas-phase polar [4 + 1+] cycloaddition of ionized methylene to alpha-dicarbonyl compounds: synthesis of 2-unsubstituted 1,3-dioxoles." Journal of mass spectrometry : JMS vol. 41,6 (2006): 735-40. doi: https://doi.org/10.1002/jms.1029
Meurer EC, Cabrini LG, Gozzo FC, Eberlin MN. Formal gas-phase polar [4 + 1+] cycloaddition of ionized methylene to alpha-dicarbonyl compounds: synthesis of 2-unsubstituted 1,3-dioxoles. J Mass Spectrom. 2006 Jun;41(6):735-40. doi: 10.1002/jms.1029. PMID: 16604574.
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Facile conversion of o-quinones into 1,3-dioxoles.

Organic letters

Batanero B, Barba F.
PMID: 15957892
Org Lett. 2005 Jun 23;7(13):2567-9. doi: 10.1021/ol050614e.

[reaction: see text] o-Quinones are transformed into the corresponding 1,3-dioxoles in a single-step process by cathodic reduction in dichloromethane.

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Batanero B, Barba F. Facile conversion of o-quinones into 1,3-dioxoles. Org Lett. 2005;7(13):2567-9doi: 10.1021/ol050614e.
Batanero, B., & Barba, F. (2005). Facile conversion of o-quinones into 1,3-dioxoles. Organic letters, 7(13), 2567-9. https://doi.org/10.1021/ol050614e
Batanero, Belen, and Barba, Fructuoso. "Facile conversion of o-quinones into 1,3-dioxoles." Organic letters vol. 7,13 (2005): 2567-9. doi: https://doi.org/10.1021/ol050614e
Batanero B, Barba F. Facile conversion of o-quinones into 1,3-dioxoles. Org Lett. 2005 Jun 23;7(13):2567-9. doi: 10.1021/ol050614e. PMID: 15957892.
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α-Glucosidase inhibitors from a mangrove associated fungus, .

BMC chemistry

Lopéz D, Cherigo L, Mejia LC, Loza-Mejía MA, Martínez-Luis S.
PMID: 31384771
BMC Chem. 2019 Feb 07;13(1):22. doi: 10.1186/s13065-019-0540-8. eCollection 2019 Dec.

No abstract available.

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Lopéz D, Cherigo L, Mejia LC, et al. α-Glucosidase inhibitors from a mangrove associated fungus, . BMC Chem. 2019;13(1):22doi: 10.1186/s13065-019-0540-8.
Lopéz, D., Cherigo, L., Mejia, L. C., Loza-Mejía, M. A., & Martínez-Luis, S. (2019). α-Glucosidase inhibitors from a mangrove associated fungus, . BMC chemistry, 13(1), 22. https://doi.org/10.1186/s13065-019-0540-8
Lopéz, Dioxelis, et al. "α-Glucosidase inhibitors from a mangrove associated fungus, ." BMC chemistry vol. 13,1 (2019): 22. doi: https://doi.org/10.1186/s13065-019-0540-8
Lopéz D, Cherigo L, Mejia LC, Loza-Mejía MA, Martínez-Luis S. α-Glucosidase inhibitors from a mangrove associated fungus, . BMC Chem. 2019 Feb 07;13(1):22. doi: 10.1186/s13065-019-0540-8. eCollection 2019 Dec. PMID: 31384771; PMCID: PMC6661824.
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An Approach Toward Oxidopyrylium Ylides Using Rh(II)-Catalyzed Cyclization Chemistry.

Tetrahedron letters

Padwa A, Boonsombat J, Rashatasakhon P.
PMID: 20953288
Tetrahedron Lett. 2007 Aug 20;48(34):5938-5941. doi: 10.1016/j.tetlet.2007.06.118.

The Rh(II)-catalyzed reaction of the E-isomer of 2-diazo-3,6-dioxo-6-phenyl-hex-enoic acid methyl ester was carried out in the presence of various carbonyl compounds and was found to give 1,3-dioxoles in moderate to good yield. In an attempt to prepare the starting...

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Padwa A, Boonsombat J, Rashatasakhon P. An Approach Toward Oxidopyrylium Ylides Using Rh(II)-Catalyzed Cyclization Chemistry. Tetrahedron Lett. 2007;48(34):5938-5941doi: 10.1016/j.tetlet.2007.06.118.
Padwa, A., Boonsombat, J., & Rashatasakhon, P. (2007). An Approach Toward Oxidopyrylium Ylides Using Rh(II)-Catalyzed Cyclization Chemistry. Tetrahedron letters, 48(34), 5938-5941. https://doi.org/10.1016/j.tetlet.2007.06.118
Padwa, Albert, et al. "An Approach Toward Oxidopyrylium Ylides Using Rh(II)-Catalyzed Cyclization Chemistry." Tetrahedron letters vol. 48,34 (2007): 5938-5941. doi: https://doi.org/10.1016/j.tetlet.2007.06.118
Padwa A, Boonsombat J, Rashatasakhon P. An Approach Toward Oxidopyrylium Ylides Using Rh(II)-Catalyzed Cyclization Chemistry. Tetrahedron Lett. 2007 Aug 20;48(34):5938-5941. doi: 10.1016/j.tetlet.2007.06.118. PMID: 20953288; PMCID: PMC2955265.
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A facile construction of oxygen heterocycles by the reaction of benzoxepine-4-carboxylates with dihaloalkanes and activated alkynes.

Organic & biomolecular chemistry

Kasagani VP, Kurma SH, Bhimapaka CR.
PMID: 31237599
Org Biomol Chem. 2019 Jul 21;17(27):6645-6653. doi: 10.1039/c9ob00769e. Epub 2019 Jun 25.

This manuscript describes the preparation of heterocyclic compounds such as naphtho[1,3]-dioxoles (3a-h), [1,4]-dioxines (4a-h), [1,4]-dioxepines (5a-c), [1,4]-dioxocines (6a-c) and diethyl 2-(2-ethoxy-2-oxoethyl)naphtho[1,3]dioxoles (8a-f). These heterocyclic compounds have been achieved by the reaction of benzoxepine-4-carboxylates (1a-h) with dihaloalkanes (2a-e) and activated...

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Kasagani VP, Kurma SH, Bhimapaka CR. A facile construction of oxygen heterocycles by the reaction of benzoxepine-4-carboxylates with dihaloalkanes and activated alkynes. Org Biomol Chem. 2019;17(27):6645-6653doi: 10.1039/c9ob00769e.
Kasagani, V. P., Kurma, S. H., & Bhimapaka, C. R. (2019). A facile construction of oxygen heterocycles by the reaction of benzoxepine-4-carboxylates with dihaloalkanes and activated alkynes. Organic & biomolecular chemistry, 17(27), 6645-6653. https://doi.org/10.1039/c9ob00769e
Kasagani, Veera Prasad, et al. "A facile construction of oxygen heterocycles by the reaction of benzoxepine-4-carboxylates with dihaloalkanes and activated alkynes." Organic & biomolecular chemistry vol. 17,27 (2019): 6645-6653. doi: https://doi.org/10.1039/c9ob00769e
Kasagani VP, Kurma SH, Bhimapaka CR. A facile construction of oxygen heterocycles by the reaction of benzoxepine-4-carboxylates with dihaloalkanes and activated alkynes. Org Biomol Chem. 2019 Jul 21;17(27):6645-6653. doi: 10.1039/c9ob00769e. Epub 2019 Jun 25. PMID: 31237599.
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Experimental Evidence of Dioxole Unimolecular Decay Pathway for Isoprene-Derived Criegee Intermediates.

The journal of physical chemistry. A

Vansco MF, Caravan RL, Zuraski K, Winiberg FAF, Au K, Trongsiriwat N, Walsh PJ, Osborn DL, Percival CJ, Khan MAH, Shallcross DE, Taatjes CA, Lester MI.
PMID: 32255634
J Phys Chem A. 2020 May 07;124(18):3542-3554. doi: 10.1021/acs.jpca.0c02138. Epub 2020 Apr 22.

Ozonolysis of isoprene, one of the most abundant volatile organic compounds emitted into the Earth's atmosphere, generates two four-carbon unsaturated Criegee intermediates, methyl vinyl ketone oxide (MVK-oxide) and methacrolein oxide (MACR-oxide). The extended conjugation between the vinyl substituent and...

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Vansco MF, Caravan RL, Zuraski K, et al. Experimental Evidence of Dioxole Unimolecular Decay Pathway for Isoprene-Derived Criegee Intermediates. J Phys Chem A. 2020;124(18):3542-3554doi: 10.1021/acs.jpca.0c02138.
Vansco, M. F., Caravan, R. L., Zuraski, K., Winiberg, F. A. F., Au, K., Trongsiriwat, N., Walsh, P. J., Osborn, D. L., Percival, C. J., Khan, M. A. H., Shallcross, D. E., Taatjes, C. A., & Lester, M. I. (2020). Experimental Evidence of Dioxole Unimolecular Decay Pathway for Isoprene-Derived Criegee Intermediates. The journal of physical chemistry. A, 124(18), 3542-3554. https://doi.org/10.1021/acs.jpca.0c02138
Vansco, Michael F, et al. "Experimental Evidence of Dioxole Unimolecular Decay Pathway for Isoprene-Derived Criegee Intermediates." The journal of physical chemistry. A vol. 124,18 (2020): 3542-3554. doi: https://doi.org/10.1021/acs.jpca.0c02138
Vansco MF, Caravan RL, Zuraski K, Winiberg FAF, Au K, Trongsiriwat N, Walsh PJ, Osborn DL, Percival CJ, Khan MAH, Shallcross DE, Taatjes CA, Lester MI. Experimental Evidence of Dioxole Unimolecular Decay Pathway for Isoprene-Derived Criegee Intermediates. J Phys Chem A. 2020 May 07;124(18):3542-3554. doi: 10.1021/acs.jpca.0c02138. Epub 2020 Apr 22. PMID: 32255634.
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Showing 1 to 7 of 7 entries