01502nam 2200361 n 450 99639360360331620221108071211.0(CKB)4940000000114488(EEBO)2240927347(UnM)9959335800971(EXLCZ)99494000000011448820790922d1726 uy engurbn||||a|bb|A brief case of the distillers[electronic resource] and of the distilling trade in England, shewing how far it is the interest of England to encourage the said trade, as it is so considerable an advantage to the landed interest, to the trade and navigation, to the publick revenue, and to the employment of the poor. Humbly recommended to the Lords and Commons of Great Britain, in the present Parliament assembledLondon Printed for T. Warner at the Black-Boy in Pater-noster-rowM.DCC.XXVI. [1726]viii, 52 pAttributed variously to Daniel Defoe.Reproduction of original in the British Library.eebo-0018Brewing industryEarly works to 1800Trade regulationEnglandEarly works to 1800Brewing industryTrade regulationDefoe Daniel1661?-1731.69634Uk-ESUk-ESCu-RivESCStRLINBOOK996393603603316A brief case of the distillers2426687UNISA05194nam 2200637Ia 450 99620213830331620230421044556.01-281-75857-497866117585783-527-61517-23-527-61516-4(CKB)1000000000376621(EBL)482005(OCoLC)261225144(SSID)ssj0000096914(PQKBManifestationID)11116484(PQKBTitleCode)TC0000096914(PQKBWorkID)10113124(PQKB)10421445(MiAaPQ)EBC482005(EXLCZ)99100000000037662119951010d1996 uy 0engur|n|---|||||txtccrActive metals[electronic resource] preparation, characterization, applications /edited by Alois FürstnerWeinheim ;New York VCHc19961 online resource (486 p.)Description based upon print version of record.3-527-29207-1 Includes bibliographical references and indexes.Active Metals; Preface; Contents; List of Contributors; 1 Rieke Metals : Highly Reactive Metal Powders Prepared by Alkali Metal Reduction of Metal Salts; 1.1 Introduction; 1.1.1 Physical Characteristics of Highly Reactive Metal Powders; 1.2 Rieke Magnesium, Calcium, Strontium, and Barium; 1.2.1 Formation of Rieke Magnesium; 1.2.2 Formation of Rieke Calcium. Strontium. and Barium; 1.2.3 Grignard Reactions Using Rieke Metals; 1.2.4 1,3-Dicne-Magnesium Reagents; 1.2.4.1 Preparation; 1.2. 4.2 Regioselcctivity1.2.4.3 Carbocyclization of (1.4-Diphenyl-2-butene-1,4-diyl)magnesium with Organic Dihalides1.2.4.4 1,2-Dimethylenecycloalkan e.Magnesium Reagents; 1.2.4.5 Synthesis of Fused Carbocycles, β, γ-Unsaturated Ketones and 3-Cyclopentenols from Conjugated Diene-Magnesium Reagents; 1.2.4.6 Synthesis of Spiro γ-Lactones and Spiro δ-Lactones from 1,3-Diene-Magnesium Reagents; 1.2.4.7 Synthesis of γ-Lactams from Conjugated Diene-Magnesium Reagents; 1.3 Rieke Zinc; 1.3.1 The Preparation of Rieke Zinc; 1.3.2 Direct Oxidative Addition of Functionalized Alkyl and Aryl Halides1.3.3 Reactions of Organozinc Reagents with Acid Chlorides1.3.4 Reactions of Organozinc Reagents with α, β-Unsaturated Ketones; 1.3.5 Reactions with Allylic and Alkynyl Halides; 1.3.6 Cross-Coupling of Vinyl and Aryl Organozinc Reagents Using a Palladium Catalyst; 1.3.7 Intramolecular Cyclizations and Conjugate Additions Mediated by Rieke Zinc; 1.3.8 Formation of Tertiary and Secondary Alkylzinc Bromides; 1.3.9 Cyanide-Based Rieke Zinc; 1.4 Organocopper Reagents Utilizing Rieke Copper; 1.4.1 Introduction; 1.4.2 Background to the Development of Rieke Copper; 1.4.3 Phosphine-Based Copper1.4.4 Lithium 2-Thienylcyanocuprate-Based Copper1.4.5 Copper Cyanide-Based Active Copper; 1.4.6 Two-Equivalent Reduction of Copper(I) Complexes : A Formal Copper Anion; 1.5 Rieke Aluminum, Indium, and Nickel; 1.5.1 Aluminum; 1.5.2 Indium; 1 5.3 Nickel; 1.6 Synthesis of Specialized Polymers and New Materials via Rieke Metals; 1.6.1 Formation of Polyarylenes Mediated by Rieke Zinc; 1.6.2 Regiocontrolled Synthesis of Poly(3-alkylthiophenes) and Related Polymers Mediated by Rieke Zinc; 1.6.3 Synthesis of Poly(phenylcarbyne) Mediated by Rieke Calcium, Strontium, or Barium1.6.4 Chemical Modification of Halogenated Polystyrenes Using Rieke Calcium or Copper1.6.5 Polymer Supported Rieke Metal Reagents and their Applications in Organic Synthesis; 2 Allylic Barium Reagents; 2.1 Introduction; 2.2 Preparation of Stereochemically Homogeneous Allylic Barium Reagents; 2.2.1 Direct Insertion Method Using Reactive Barium; 2.2.2 Stereochemical Stability; 2.2.3 Silylation of Stereochemically Homogeneous Allylic Barium Reagents; 2.2.3.1 Procedure for Generation of Reactive Barium (Ba*); 2.2.3.2 Procedure for Protonation of the Geranyl Barium Reagent2.2.3.3 Silylation of (E)-2-Decenylbarium ChlorideReactions with metals are ubiquitous in organic synthesis and, particularly in the last few years, a large repertoire of methods for the activation of metals and for their use in organic synthesis has been developed. In Active Metals, topics ranging from morphology of metal clusters and nanometallurgy to organometallic chemistry, catalysis and the use of activated metals in natural product synthesis are authoritatively discussed by leading experts in the field.Active Metals will allow you to fully benefit from the recent advances in the field by giving:* Detailed experimental pMetal activationActive metalsOrganometallic compoundsSynthesisMetal activation.Active metals.Organometallic compoundsSynthesis.546.3547.05Fürstner Alois945461MiAaPQMiAaPQMiAaPQBOOK996202138303316Active metals2134486UNISA