Relevant bibliographies by topics / Lysergol

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  1. Journal articles

Academic literature on the topic 'Lysergol'

Author: Grafiati
Published: 24 April 2022

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Journal articles on the topic "Lysergol"

1

Merkel, Stefan, Robert Köppen, Matthias Koch, Franziska Emmerling, and Irene Nehls. "Lysergol monohydrate." Acta Crystallographica Section E Structure Reports Online 68, no. 2 (2012): o523. http://dx.doi.org/10.1107/s1600536812002632.

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2

Patil, Shrikant, Manish Nivsarkar, and Sheetal Anandajiwala. "Isolation and TLC Densitometric Quantification of Lysergol from the Seeds of Ipomoea muricata (Linn.) Jacq." ISRN Chromatography 2013 (January 22, 2013): 1–6. http://dx.doi.org/10.1155/2013/134586.

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Seeds of Ipomoea muricata, well known in Ayurveda for its purgative action, contains mainly indole alkaloids. Lysergol (major alkaloid) exhibits hypotensive, psychotropic, and uterus and intestine-stimulating properties. TLC fingerprint profile of I. muricata seeds was developed using chloroform : methanol (95 : 5 v/v) as the mobile phase. Plate was visualized under UV 254 nm and UV 366 nm and after derivatization with Van Urk reagent. Lysergol resolved at . Further, TLC-densitometric method was developed and validated for quantification of Lysergol avoiding derivatization step. Ethyl acetate
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3

Harris, J. R., and D. C. Horwellt. "Conversion of Agroclavine to Lysergol." Synthetic Communications 22, no. 7 (1992): 995–99. http://dx.doi.org/10.1080/00397919208019288.

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4

Shukla, M., M. Y. Malik, S. Jaiswal, et al. "A mechanistic investigation of the bioavailability enhancing potential of lysergol, a novel bioenhancer, using curcumin." RSC Advances 6, no. 64 (2016): 58933–42. http://dx.doi.org/10.1039/c6ra09307h.

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5

Stevenson, David E., Vladimír Křen, Petr Halada та Petr Sedmera. "Enzymatic Preparation of Lysergol β-D-Glucuronide". Collection of Czechoslovak Chemical Communications 65, № 1 (2000): 117–21. http://dx.doi.org/10.1135/cccc20000117.

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6

Křen, Vladimír, and Petr Sedmera. "N-1-Trimethylsilyl Derivatives of Ergot Alkaloids." Collection of Czechoslovak Chemical Communications 61, no. 8 (1996): 1248–53. http://dx.doi.org/10.1135/cccc19961248.

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N-1-Trimethylsilyl derivatives of five different suitably protected parent ergot (clavine) alkaloids (agroclavine 1a, elymoclavine 2a, lysergol 3a, lysergene 4a, and 9,10-dihydrolysergol 5a) were prepared in 47-94% yields by refluxing the (protected) parent compounds with N-methyl-N-(trimethylsilyl)trifluoroacetamide in acetonitrile under nitrogen atmosphere.
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7

Patil, Shrikant, Ranjeet Prasad Dash, Sheetal Anandjiwala, and Manish Nivsarkar. "Simultaneous quantification of berberine and lysergol by HPLC-UV: evidence that lysergol enhances the oral bioavailability of berberine in rats." Biomedical Chromatography 26, no. 10 (2011): 1170–75. http://dx.doi.org/10.1002/bmc.2674.

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8

Stevenson, David E., Vladimir Kren, Petr Halada та Petr Sedmera. "ChemInform Abstract: Enzymatic Preparation of Lysergol β-D-Glucuronide." ChemInform 31, № 17 (2010): no. http://dx.doi.org/10.1002/chin.200017214.

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9

Inuki, Shinsuke, Shinya Oishi, Nobutaka Fujii, and Hiroaki Ohno. "Total Synthesis of (±)-Lysergic Acid, Lysergol, and Isolysergol by Palladium-Catalyzed Domino Cyclization of Amino Allenes Bearing a Bromoindolyl Group." Organic Letters 13, no. 8 (2011): 2145. http://dx.doi.org/10.1021/ol200375v.

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10

Inuki, Shinsuke, Shinya Oishi, Nobutaka Fujii, and Hiroaki Ohno. "Total Synthesis of (±)-Lysergic Acid, Lysergol, and Isolysergol by Palladium-Catalyzed Domino Cyclization of Amino Allenes Bearing a Bromoindolyl Group." Organic Letters 10, no. 22 (2008): 5239–42. http://dx.doi.org/10.1021/ol8022648.

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