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Collect. Czech. Chem. Commun. 1969, 34, 1025-1032
https://doi.org/10.1135/cccc19691025

Properties of sodium bis-(2-methoxyethoxy)aluminium hydride. III. Reduction of carboxylic acids and their derivatives

M. Černý, J. Málek, M. Čapka and V. Chvalovský

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  • Kotha Sambasivarao, Misra Shilpi, Srinivas Venu: Diversity Oriented Approach to Polycyclic Compounds through the Diels–Alder Reaction and the Suzuki Coupling. Eur J Org Chem 2012, 2012, 4052. <https://doi.org/10.1002/ejoc.201200484>
  • Parthasarathy Rajasekaran, Jenniefer Samson Jegan, Muthiah Packianathan Thomas, Sulochana Nagarajan: 2,6,6-Trimethylcyclohexene-1-carbaldehyde oxime. Acta Crystallogr E Struct Rep Online 2011, 67, o2732. <https://doi.org/10.1107/S1600536811037895>
  • Pasumansky Lubov, Goralski Christian T., Singaram Bakthan: Lithium Aminoborohydrides:  Powerful, Selective, Air-Stable Reducing Agents. Org. Process Res. Dev. 2006, 10, 959. <https://doi.org/10.1021/op0600759>
  • Miyachi Hiroyuki, Kiyota Hiromi, Uchiki Hideharu, Segawa Mitsuru: Synthesis and antimuscarinic activity of a Series of 4-(1-Imidazolyl)-2,2-diphenylbutyramides: discovery of potent and subtype-selective antimuscarinic agents. Bioorganic & Medicinal Chemistry 1999, 7, 1151. <https://doi.org/10.1016/S0968-0896(99)00003-6>
  • Yang Cangming, Pittman Charles U.: Dechlorination of Pentachlorophenol and 1,2,4-Trichlorobenzene Using NaBH4and NaBH4/LiCl AT 125–315°C in Glyme Solvents. Synthetic Communications 1998, 28, 517. <https://doi.org/10.1080/00397919808005107>
  • Bandgar B. P., Modhave R. K., Wadgaonkar P. P., Sande A. R.: Selective reduction of mixed anhydrides of carboxylic acids to alcohols using borohydride exchange resin (BER)–nickel acetate. J. Chem. Soc., Perkin Trans. 1 1996, 1993. <https://doi.org/10.1039/P19960001993>
  • Wells Andy: Sodium BIS(2-Methoxyethoxy)Aluminium Hydride in Petroleum Ether; A Reagent for the Selective Reduction of Brominated Fatty Esters to Bromo Alcohols. Synthetic Communications 1996, 26, 1143. <https://doi.org/10.1080/00397919608003721>
  • Robyr P., Tomaselli M., Straka J., Grob-Pisano C., Suter U.W., Meier B.H., Ernst R.R.: RF-driven and proton-driven NMR polarization transfer for investigating local order. Molecular Physics 1995, 84, 995. <https://doi.org/10.1080/00268979500100691>
  • Patwardhan Sarita A.: SYNTHESIS OF α,ω-ALKANEDIOLS. A REVIEW. Organic Preparations and Procedures International 1994, 26, 645. <https://doi.org/10.1080/00304949409458163>
  • Fisher Gary B., Harrison John, Fuller Joseph C., Goralski Christian T., Singaram Bakthan: Synthesis and characterization of lithium aminoborohydrides: A new class of powerful reducing agents. Tetrahedron Letters 1992, 33, 4533. <https://doi.org/10.1016/S0040-4039(00)61305-9>
  • Takahashi Kyoko, Shibagaki Makoto, Matsushita Hajime: Reduction of Dicarboxylic Acid Anhydride with 2-Propanol over Hydrous Zirconium Oxide. Bulletin of the Chemical Society of Japan 1992, 65, 262. <https://doi.org/10.1246/bcsj.65.262>
  • Kamochi Yasuko, Kudo Tadahiro: Lanthanoids in Organic Synthesis. I. The Novel Reduction of Carboxylic Acids with Samarium Diiodide-Base System. Bulletin of the Chemical Society of Japan 1992, 65, 3049. <https://doi.org/10.1246/bcsj.65.3049>
  • Kamochi Yasuko, Kudo Tadahiro: Novel Reduction of Carboxylic Acids with Samarium Diiodide. Chemistry Letters 1991, 20, 893. <https://doi.org/10.1246/cl.1991.893>
  • Kirchner Eike, Thiem Frauke, Dernick Rudolt, Heukeshoven Jochen, Thieina Joachim: Studies on the Glycosylation ofN-Acetylneuraminic Acid. Journal of Carbohydrate Chemistry 1988, 7, 453. <https://doi.org/10.1080/07328308808058936>
  • Prelog Vladimir, Bedeković Davor: Chirale 2,2′‐Polyoxaalkano‐9,9′‐spirobifluorene. Helvetica Chimica Acta 1979, 62, 2285. <https://doi.org/10.1002/hlca.19790620725>
  • Balba H. M., Still Gerald G.: Synthesis of 14C-coniferyl alcohol (4-hydroxy-3-methoxycinnamyl alcohol). J Label Compd Radiopharm 1978, 15, 309. <https://doi.org/10.1002/jlcr.2580150136>
  • Hallgren Bo, Ställberg Gunnel, Boeryd Bernt: Occurrence, synthesis and biological effects of substituted glycerol ethers. Progress in the Chemistry of Fats and other Lipids 1978, 16, 45. <https://doi.org/10.1016/0079-6832(78)90036-8>
  • Angelo Helle Riis, Christensen Jytte Molin: Gas chromatographic method for the determination of dextropropoxyphene and nordextropropoxyphene in human plasma, serum and urine. Journal of Chromatography A 1977, 140, 280. <https://doi.org/10.1016/S0021-9673(00)93591-X>
  • Storck Winfried, Manecke Georg: Modellsubstanzen für polymere Redoxsysteme, 8. Tetra‐ und hexavalente Redoxsysteme vom 1,4‐Benzochinon‐Typus. Makromol. Chem. 1975, 176, 97. <https://doi.org/10.1002/macp.1975.021760108>
  • Herz J. E., Cruz S. M.: THE SYNTHESIS OF STEROLS WITH MODIFIED SIDE CHAINS BY THE WITTIG REACTION. Organic Preparations and Procedures International 1975, 7, 16. <https://doi.org/10.1080/00304947509356807>
  • KIRSCHNER Kasper, WISKOCIL Robert L., FOEHN Martha, REZEAU Laurel: The Tryptophan Synthase from Escherichia coli. European Journal of Biochemistry 1975, 60, 513. <https://doi.org/10.1111/j.1432-1033.1975.tb21030.x>
  • Klásek A., Šantavý F., Duffield M. A., Reichstein T.: Alkaloide aus Evonymus europaea L. Helvetica Chimica Acta 1971, 54, 2144. <https://doi.org/10.1002/hlca.19710540749>