Borane–tetrahydrofuran is a dipolar bond charge-transfer complex composed of borane and tetrahydrofuran (THF). and National Institute of General Medical Sciences of the National Institutes of Health under grant R01GM133198. [1], The complex is commercially available but can also be generated by the dissolution of diborane in THF. Find out more about how we use your information in our Privacy Policy and Cookie Policy. You can change your choices at any time by visiting Your Privacy Controls. [5], The solution is highly sensitive to air, requiring the use of air-free techniques. ANTI-BAK (BH3 DOMAIN SPECIFIC) antibody produced in rabbit. Would it be nitrogen trioxide and boron trihydrogen? "A Simple And Convenient Method For The Oxidation Of Organoboranes Using Sodium Perborate: (+)-isopinocampheol", https://en.wikipedia.org/w/index.php?title=Borane–tetrahydrofuran&oldid=863350344, Pages using collapsible list with both background and text-align in titlestyle, Articles containing unverified chemical infoboxes, Creative Commons Attribution-ShareAlike License, This page was last edited on 10 October 2018, at 06:46. valinol). Yahoo is part of Verizon Media. 0 0. Answer Save. Favorite Answer. The Bcl-2 homology domain 3; This disambiguation page lists articles associated with the same title formed as a letter-number combination. [4] The following organoboron reagents are prepared from borane-THF: 9-borabicyclo[3.3.1]nonane, Alpine borane, diisopinocampheylborane. BH3 could refer to The molecule borane, which has a chemical formula of BH 3. [1], Except where otherwise noted, data are given for materials in their. yes, those are correct. Information about your device and internet connection, including your IP address, Browsing and search activity while using Verizon Media websites and apps. 1 decade ago. Bortrifluorid kann gewonnen werden durch: Reaktion von Bortrioxid mit Flusssäure: + + im großtechnischen Bereich durch Erhitzen von Dibortrioxid oder Borax mit Calciumfluorid und konzentrierter Schwefelsäure; im Labor durch Thermolyse von Diazonium tetrafluoroboraten; weiter aus Natrium-oder Ammoniumtetrafluoroborat mit Bortrioxid in Schwefelsäure and the National Cancer Institute, It adds across alkenes to give organoboron compounds that are useful intermediates. [2], The complex can reduce carboxylic acids to alcohols and is a common route for the reduction of amino acids to amino alcohols[3] (e.g. To enable Verizon Media and our partners to process your personal data select 'I agree', or select 'Manage settings' for more information and to manage your choices. Anonymous . 2 Answers. RCSB PDB is funded by Marek Zaidlewicz, Herbert C. Brown, Santhosh F. Neelamkavil, "Borane–Tetrahydrofuran" Encyclopedia of Reagents for Organic Synthesis, 2008 John Wiley & Sons. Lexie. Predicted data is generated using the US Environmental Protection Agency’s EPISuite™. 2) Borane. mol −1 : Appearance White solid Melting point: 66 °C (151 °F; 339 K) H225, H260, H302, H315, H318, H319, H335 Ammonia borane (also systematically named amminetrihydridoboron), also called borazane, is the chemical compound with the formula H 3 NBH 3.The colourless or white solid is the simplest molecular boron-nitrogen-hydride compound. 6 years ago. It is also used as a source of borane (BH3) for the formation of adducts. 2)BH3. National Institute of Allergy and Infectious Diseases, View summary at Ligand Expo. the National Science Foundation (DBI-1832184), If an internal link led you here, you may wish to … Source(s): CHEM major in … Find related ligands: Stereoisomers Similar ligands Chemical Structure Search. These solutions are used for reductions and hydroboration, reactions that are useful in synthesis of organic compounds.