Relevant bibliographies by topics / Hydrure de diisobutylaluminium [DIBAL-H]

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  1. Journal articles
  2. Dissertations / Theses

Academic literature on the topic 'Hydrure de diisobutylaluminium [DIBAL-H]'

Author: Grafiati
Published: 4 June 2021
Last updated: 1 February 2022

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Journal articles on the topic "Hydrure de diisobutylaluminium [DIBAL-H]"

1

Xia, Yamu, Zhen Mo, Lin Sun, et al. "First total synthesis of quiquesetinerviusin A." Journal of Chemical Research 41, no. 5 (2017): 296–300. http://dx.doi.org/10.3184/174751917x14931195075599.

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The first total synthesis of the dihydrobenzofuran neolignan quiquesetinerviusin A and its related structure have been described. Phenolic coupling is the key step to constructing the dihydrobenzofuran skeleton with vanillin as the raw material. The hydroxyl group was protected with dihydropyran (DHP) and the ester group was reduced with diisobutylaluminium hydride (DIBAL-H) in order to obtain the crucial intermediate diol, which was then condensed with an acid ligand to give the desired compounds following removal of the protecting groups.
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Meng, Xiangbao, Yongmin Zhang, Matthieu Sollogoub, and Pierre Sinaÿ. "Diisobutylaluminium hydride (DIBAL-H) as a molecular scalpel: a new mechanistic proposal for a spiroketal rearrangement." Tetrahedron Letters 45, no. 44 (2004): 8165–68. http://dx.doi.org/10.1016/j.tetlet.2004.09.030.

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Xiao, Sulong, Ming Yang, Pierre Sinaÿ, Yves Blériot, Matthieu Sollogoub та Yongmin Zhang. "Diisobutylaluminium Hydride (DIBAL-H) Promoted Secondary Rim Regioselective Demethylations of Permethylated β-Cyclodextrin: A Mechanistic Proposal". European Journal of Organic Chemistry 2010, № 8 (2010): 1510–16. http://dx.doi.org/10.1002/ejoc.200901230.

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4

Zaborova, Elena, Yves Blériot та Matthieu Sollogoub. "μ-Waves avoid large excesses of diisobutylaluminium-hydride (DIBAL-H) in the debenzylation of perbenzylated α-cyclodextrin". Tetrahedron Letters 51, № 9 (2010): 1254–56. http://dx.doi.org/10.1016/j.tetlet.2009.12.037.

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Bistri, Olivia, Pierre Sinaÿ та Matthieu Sollogoub. "Diisobutylaluminium hydride (DIBAL-H) is promoting a selective clockwise debenzylation of perbenzylated 6A,6D-dideoxy-α-cyclodextrin". Tetrahedron Letters 46, № 45 (2005): 7757–60. http://dx.doi.org/10.1016/j.tetlet.2005.09.046.

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6

Fernández-Bachiller, Isabel. "Diisobutylaluminun Hydride (DIBAL-H)." Synlett 2002, no. 01 (2002): 0179–80. http://dx.doi.org/10.1055/s-2002-19347.

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Hayashi, Masahiko, Tomoko Yoshiga, Kanako Nakatani, Kazuyuki Ono та Nobuki Oguni. "Reduction of α-trialkylsiloxy nitriles with diisobutylaluminium hydride (DIBAH): A facile preparation of α-trialkylsiloxy aldehydes and their derivatives". Tetrahedron 50, № 9 (1994): 2821–30. http://dx.doi.org/10.1016/s0040-4020(01)86995-7.

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HAYASHI, M., T. YOSHIGA, K. NAKATANI, K. ONO та N. OGUNI. "ChemInform Abstract: Reduction of α-Trialkylsiloxy Nitriles with Diisobutylaluminum Hydride (DIBAH): A Facile Preparation of α-Trialkylsiloxy Aldehydes and Their Derivatives". ChemInform 25, № 27 (2010): no. http://dx.doi.org/10.1002/chin.199427059.

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9

Dezember, Thomas, and Helmut Sitzmann. "Die Fulven-Route zum Pentaisopropylcyclopentadienid / The Fulvene Route to Pentaisopropylcyclopentadienide." Zeitschrift für Naturforschung B 52, no. 8 (1997): 911–18. http://dx.doi.org/10.1515/znb-1997-0805.

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Sodium tetraisopropylcyclopentadienide (2) is attacked selectively in 5-position by tosyl azide with formation of 5-diazo-1,2,3,4-tetraisopropylcyclopentadiene (1) and also by the iminium salt [Me2NC(H)OMe]+ MeOSO3- to yield 1,2,3,4-tetraisopropyl-6-dimethylamino-pentafulvene (3) with concomitant methanol elimination. In a one pot reaction 3 adds methyllithium to form a cyclopentadienide intermediate (4) which is converted in situ to 1,2,3,4- tetraisopropyl-6-methyl-pentafulvene (5) with dimethylchlorosilane. By the same procedure with 1,4-dilithiobutane instead of methyllithium two tetraisoproylfulvene moieties are linked to the bis-fulvene 8 with a -(CH2)4- backbone. 3 can be converted directly to 1,2,3,4- tetraisopropylpentafulvene (7) with diisobutylaluminum hydride. 5 again adds methyllithium to give lithium pentaisopropylcyclopentadienide (6) or can be deprotonated at the 6-methyl group with potassium hydride. The intermediate potassium salt gives 1,2,3,4-tetraisopropyl- 6-trimethylsilylmethyl-pentafulvene (9) with trimethylchlorosilane. The fulvene 7 could be η6-coordinated to the tricarbonyl chromium complex 10 with [Cr(CO)3(NCEt)3], 5 and 7 yield the molybdenum analogues 11 and 12 with [Mo(CO)3(NCEt)3].
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Friebe, Lars, Oskar Nuyken, Heike Windisch, and Werner Obrecht. "Polymerization of 1,3-Butadiene Initiated by Neodymium Versatate/Diisobutylaluminium Hydride/Ethylaluminium Sesquichloride: Kinetics and Conclusions About the Reaction Mechanism." Macromolecular Chemistry and Physics 203, no. 8 (2002): 1055. http://dx.doi.org/10.1002/1521-3935(20020501)203:8<1055::aid-macp1055>3.0.co;2-h.

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Dissertations / Theses on the topic "Hydrure de diisobutylaluminium [DIBAL-H]"

1

Lecourt, Thomas. "Débenzylation régiosélective des cyclodextrines : mécanisme réactionnel et application à la synthèse d'oligomères cycliques." Paris 6, 2003. http://www.theses.fr/2003PA066183.

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