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Synthetic Communications
An International Journal for Rapid Communication of Synthetic Organic Chemistry
Volume 28, 1998 - Issue 1
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Original Articles

Synthesis of (25R)-5α-Spirostan-2α,3α,6β-triol TriacetateFootnote#

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Pages 75-81 | Received 02 Jun 1997, Published online: 20 Aug 2006

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Read on this site (2)

MartínA. Iglesias Arteaga, Roxana Perez Gil, CarlosS. Pérez Martínez & Francisco Coll Manchado. (2000) Synthetic Steroidal Sapogenins. Part III1 23-Ketohecogenin and 23-Ketoisochiapagenin. Synthetic Communications 30:1, pages 163-170.
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MartinA. IglesiasArteaga, Roxana PérezGil, Vivian LeliebreLara, Francisco CollManchado & CarlosS. PérezMartínez.. (1998) Synthesis of (25R)-2α,3α-Epoxy-5α-Spirostan-6,23-Dione. Synthetic Communications 28:23, pages 4387-4392.
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Articles from other publishers (12)

Vanessa Aitken, Katy Diaz, Mauricio Soto, Andrés F. Olea, Mauricio A. Cuellar, Maria Nuñez & Luis Espinoza-Catalán. (2023) New Brassinosteroid Analogs with 23,24-Dinorcholan Side Chain, and Benzoate Function at C-22: Synthesis, Assessment of Bioactivity on Plant Growth, and Molecular Docking Study. International Journal of Molecular Sciences 25:1, pages 419.
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Daylin Fernández Pacheco, Leonardo González Ceballos, Armando Zaldo Castro, Marcos R. Conde González, Laura González de la Torre, Lia Pérez Rostgaard, Luis Espinoza, Katy Díaz, Andrés F. Olea & Yamilet Coll García. (2021) Synthesis of New Steroidal Carbamates with Plant-Growth-Promoting Activity: Theoretical and Experimental Evidence. International Journal of Molecular Sciences 22:5, pages 2330.
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Katy Díaz, Luis Espinoza, Rodrigo Carvajal, Marcos Conde-González, Vladimir Niebla, Andrés F. Olea & Yamilet Coll. (2020) Biological Activities and Molecular Docking of Brassinosteroids 24-Norcholane Type Analogs. International Journal of Molecular Sciences 21:5, pages 1832.
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Jocelyn Oyarce, Vanessa Aitken, César González, Karoll Ferrer, Andrés F. Olea, Teodor Parella & Luis Espinoza Catalán. (2019) Synthesis and Structural Determination of New Brassinosteroid 24-Nor-5α-Cholane Type Analogs. Molecules 24:24, pages 4612.
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Reyna Zeferino-Diaz, J. Ciciolil Hilario-Martinez, Maricela Rodriguez-Acosta, Alan Carrasco-Carballo, Maria Guadalupe Hernandez-Linares, Jesus Sandoval-Ramirez & Maria A. Fernandez-Herrera. (2017) Mimicking natural phytohormones. 26-Hydroxycholestan-22-one derivatives as plant growth promoters. Steroids 125, pages 20-26.
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Lai-King Sy, Chun-Nam Lok, Juan-Yu Wang, Yungen Liu, Lu Cheng, Pui-Ki Wan, Chi-Ting Leung, Bei Cao, Wai-Lun Kwong, Raymond Chuen-Chung Chang & Chi-Ming Che. (2016) Identification of “sarsasapogenin-aglyconed” timosaponins as novel Aβ-lowering modulators of amyloid precursor protein processing. Chemical Science 7:5, pages 3206-3214.
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Anielka Rosado-Abon, Nuria Esturau-Escofet, Marcos Flores-Álamo, Rafael Moreno-Esparza & Martín A. Iglesias-Arteaga. (2013) The Crystal Structure of Diosgenin Acetate and Its 23-Oxygenated Derivatives. Journal of Chemical Crystallography 43:4, pages 187-196.
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Susana Rincón, Rebeca Yépez, M. Eugenia Ochoa, Yliana López, Rosa Santillan & Norberto Farfán. (2012) (25 R )-16β-Acetoxy-3β-bromo-23′,26-epoxy-23′,25-dimethyl-5α-cholest-23,23′-en-6-one dichloromethane monosolvate . Acta Crystallographica Section E Structure Reports Online 68:12, pages o3260-o3261.
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Martı́n A Iglesias-Arteaga, Carlos Pérez Martı́nez & Francisco Coll Manchado. (2002) Spirostanic analogues of castasterone. Steroids 67:3-4, pages 159-163.
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Martin A. Iglesias-Arteaga, Carlos Pérez Martínez & Francisco Coll Manchado. (2019) Main NMR Characteristics of Synthetic (25r)-5α-furostanes. Journal of Chemical Research 2001:1, pages 34-35.
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O. Au-Alvarez, R.C. Peterson, M. A. Iglesias Arteagas, R. Perez Gil, F. Coll Manchado & R. Pomes Hernandez. (2000) The crystal structure of (23R, 25S)-3β-bromo-6β-acetoxy-5α-spirostan-23-ol monohydrate. Zeitschrift für Kristallographie - Crystalline Materials 215:3, pages 179-181.
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M. A. IGLESIAS ARTEAGA, R. PEREZ GIL, V. LELIEBRE LARA, F. COLL MANCHADO & C. S. PEREZ MARTINEZ. (2010) ChemInform Abstract: Synthesis of (25R)‐5α‐Spirostan‐2α,3α,6β‐triol Triacetate.. ChemInform 29:21.
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