LEADER 02809nam 2200421 n 450 001 996395699803316 005 20231114205033.0 035 $a(CKB)4330000000315106 035 $a(EEBO)2240883698 035 $a(UnM)9927732700971 035 $a(UnM)99828093 035 $a(EXLCZ)994330000000315106 100 $a19950329d1666 uy | 101 0 $aeng 135 $aurbn#|||a|bb| 200 02$aA display of herauldry$b[electronic resource] $emanifesting a more easie access to the knowledge thereof then hath hitherto been published by any, through the benefit of method; wherein it is now reduced by the study and industry of John Guillim late Pursuivant at Arms. Interlaced with much variety of history, suitable to the several occasions or subjects 205 $aThe sixth edition. Corrected and much enlarged by the author himself in his life time: together with his own addition of explaining the terms of hawking and hunting. And in this sixth edition are all the names and coats of arms of the Knights of the Garter, Knights Baronets, and Knights of the Bath: together with the atchievements at large of most of the nobility which were made by King Charles the Second. And whereas in the fourth edition there were several offensive coats to the loyal party, they are in this sixth exploded, and a supply of several of His Majesties friends. 210 $aLondon $cprinted by J.B. for John Williams at the Crown and Globe, and Joshua Kirton at the Kings Arms in St. Pauls Church-yard; Humphrey Tuckey at the Black Spread-Eagle, and Francis Tyton at the Three Daggers in Fleetstreet$d1666 215 $a[20], 368, 445-446, 369-402, [14], 403-460, p. 443, p. 144, 36, [6], 37-114, [8] p. $cill. (woodcuts) 300 $aAnother edition of: Guillim, John. A display of heraldrie. 300 $aWith several indices. 300 $aText continuous, apart from the extra leaf misbound between pp. 368-369. Of the [14] p. inserted between pp. 402-403, the first 10 are numbered "402"and given signatures: [*], [**], [***] (-3*2), the last 4 are unnumbered and signed correctly; the register is continuous to the beginning of the 36 p. "Exact register" of the Knights and Baronets. 300 $aRunning title of main text: Display of heraldry. 300 $aTitle page and text rubricated. 300 $aWoodcuts are of heraldic devices and coats of arms. 300 $aReproduction of the original in the British Library. 330 $aeebo-0018 606 $aHeraldry$zGreat Britain$vEarly works to 1800 615 0$aHeraldry 700 $aGuillim$b John$f1565-1621.$0793396 801 0$bCu-RivES 801 1$bCu-RivES 801 2$bCStRLIN 801 2$bWaOLN 906 $aBOOK 912 $a996395699803316 996 $aA display of herauldry$92339813 997 $aUNISA LEADER 05368nam 2200697Ia 450 001 9911019856003321 005 20200520144314.0 010 $a9786611947170 010 $a9781281947178 010 $a1281947172 010 $a9783527623235 010 $a352762323X 010 $a9783527623242 010 $a3527623248 035 $a(CKB)1000000000556195 035 $a(EBL)481568 035 $a(OCoLC)283799101 035 $a(SSID)ssj0000216329 035 $a(PQKBManifestationID)11197412 035 $a(PQKBTitleCode)TC0000216329 035 $a(PQKBWorkID)10197084 035 $a(PQKB)10014171 035 $a(MiAaPQ)EBC481568 035 $a(Perlego)2772661 035 $a(EXLCZ)991000000000556195 100 $a20080215d2008 uy 0 101 0 $aeng 135 $aur|n|---||||| 181 $ctxt 182 $cc 183 $acr 200 00$aOrganosulfur chemistry in asymmetric synthesis /$fedited by Takeshi Toru and Carsten Bolm 210 $aWeinheim $cWiley-VCH$dc2008 215 $a1 online resource (450 p.) 300 $aDescription based upon print version of record. 311 08$a9783527318544 311 08$a3527318542 320 $aIncludes bibliographical references and index. 327 $aOrganosulfur Chemistry in Asymmetric Synthesis; Contents; Preface; List of Contributors; 1 Asymmetric Synthesis of Chiral Sulfoxides; 1.1 Chiral Sulfoxides; 1.1.1 Introduction; 1.1.2 The Main Routes to Chiral Sulfoxides; 1.2 Use of Chiral Sulfur Precursors; 1.2.1 Sulfinates (Andersen Method); 1.2.2 Diastereoselective Formation of Sulfinates; 1.2.3 Sulfinates from Sulfites; 1.2.4 Sulfinamides; 1.3 Catalytic Enantioselective Sulfide Oxidation; 1.3.1 Titanium Complexes; 1.3.1.1 Diesters of Tartaric Acid; 1.3.1.2 C(2)-Symmetric 1,2-Diols as Ligands; 1.3.1.3 Binaphthol and Derivatives 327 $a1.3.1.4 C(3)-Symmetric Triethanolamine Ligands1.3.1.5 Ti (Salen) Catalysts; 1.3.2 Manganese Complexes; 1.3.3 Vanadium Complexes; 1.3.4 Molybdenum Complexes; 1.3.5 Iron Complexes; 1.3.6 Miscellaneous; 1.4 Catalytic Arylation of Sulfenate Anions; 1.5 Enantioselective Oxidation of Sulfides; 1.6 Summary; References; 2 Asymmetric Synthesis of Optically Active Sulfinic Acid Esters; 2.1 Introduction; 2.2 Enantiomeric Sulfinic Acid Esters; 2.3 Diastereomeric Sulfinic Acid Esters; References; 3 Asymmetric Transformations Mediated by Sulfinyl Groups; 3.1 Introduction 327 $a3.2 Nucleophilic Additions to C=O and C=N Bonds Mediated by ?-Sulfinyl Groups3.2.1 ?-Ketosulfoxides; 3.2.1.1 Reduction Reactions; 3.2.1.2 Alkylation Reactions; 3.2.1.3 Aldol Reaction with ?-Ketosulfoxides Acting as Electrophiles; 3.2.1.4 Hydrocyanation Reactions; 3.2.2 ?-Imino(enamino)sulfoxides; 3.3 Conjugate Additions to ?,?-Unsaturated Sulfoxides; 3.3.1 Nucleophilic Additions; 3.3.1.1 (E) and (Z)-2-Substituted Vinyl Sulfoxides; 3.3.1.2 1-Substituted Vinyl Sulfoxides; 3.3.2 Tandem Reactions; 3.3.3 Radical Conjugate Additions and Other Reactions; 3.4 Cycloadditions 327 $a3.4.1 Asymmetric Diels-Alder Reactions3.4.1.1 Sulfinyl Dienophiles; 3.4.1.2 Sulfinyl Dienes; 3.4.2 Asymmetric Hetero Diels-Alder Reactions; 3.4.3 Asymmetric 1,3-Dipolar Cycloadditions; 3.4.3.1 Reactions with Nitrones; 3.4.3.2 Reactions with Azomethine Ylides; 3.4.3.3 Reactions with Nitrile Oxides; 3.4.3.4 Reactions with Diazoalkanes; 3.4.3.5 Reactions with Other Dipoles; 3.4.4 Other Asymmetric Cycloadditions; 3.5 Asymmetric Processes Stereocontrolled by Remote Sulfoxides; 3.5.1 Nucleophilic Processes; 3.5.1.1 Reactions with Sulfinylated Electrophiles 327 $a3.5.1.2 Reactions with Sulfinylated Nucleophiles3.6 Asymmetric Pummerer Reaction; References; 4 Synthesis and Applications of Chiral Dithioacetal Derivatives; 4.1 Introduction; 4.2 Lithiated Dithianes; 4.3 Alternative Methods; 4.4 Oxidation Methods for the Construction of Chiral Dithioacetal Derivatives and Applications in Synthesis; 4.5 Applications of Chiral Dithioacetal Derivatives in Natural Product and Biologically Active Compound Synthesis; 4.6 Summary; References; 5 Synthesis and Use of Chiral Sulfur Ylides; 5.1 Introduction; 5.1.1 Reactions of Sulfonium Ylides 327 $a5.1.2 Methods of Preparation 330 $aIn this first book to gather the information on this hot topic otherwise widely spread throughout the literature, experienced editors and top international authors cover everything the reader needs -- from the synthesis of chiral organosulfur compounds to applications and catalysis: * Asymmetric synthesis of chiral sulfinates and sulfoxides* Synthesis and use of chiral dithioacetal derivatives, ylids, chiral sulfoximines and sulfinamides* Use of chiral sulfoxides as ligands in catalysis* Asymmetric reactions of alpha-sulfenyl, alpha-sulfinyl and alpha-sulfonyl carbanions.As 606 $aOrganosulfur compounds 606 $aAsymmetric synthesis 606 $aEnantioselective catalysis 615 0$aOrganosulfur compounds. 615 0$aAsymmetric synthesis. 615 0$aEnantioselective catalysis. 676 $a547.06045 701 $aToru$b Takeshi$01840432 701 $aBolm$b Carsten$0542970 801 0$bMiAaPQ 801 1$bMiAaPQ 801 2$bMiAaPQ 906 $aBOOK 912 $a9911019856003321 996 $aOrganosulfur chemistry in asymmetric synthesis$94419979 997 $aUNINA