LEADER 01519nam 2200349 n 450 001 996395746203316 005 20200824120537.0 035 $a(CKB)4330000000319476 035 $a(EEBO)2240892783 035 $a(UnM)99837018e 035 $a(UnM)99837018 035 $a(EXLCZ)994330000000319476 100 $a19900926d1554 uy | 101 0 $alat 135 $aurbn||||a|bb| 200 04$aThe historie of Wyates rebellion$b[electronic resource] $ewith the order and maner of resisting the same, wherunto in the ende is added an earnest conference with the degenerate and sedicious rebelles for the serche of the cause of their daily disorder. Made and compyled by John Proctor 210 $a[London $cRobert Caly]$dMense Decembris. Anno 1554 215 $a[8], 17 leaves, p. 18-25, leaves 26-96, [6] leaves 300 $aColophon reads: Imprynted at London by Robert Caly within the precincte of the late dissolved house of the graye freers, nowe converted to an hospitall, called Christes Hospitall. The xxii. daye of December. 1554. 300 $aText is continuous. 300 $aReproduction of the original in the British Library. 330 $aeebo-0018 607 $aGreat Britain$xHistory$yMary I, 1553-1558$vEarly works to 1800 700 $aProctor$b John$f1521?-1584.$01006307 801 0$bCu-RivES 801 1$bCu-RivES 801 2$bCStRLIN 801 2$bWaOLN 906 $aBOOK 912 $a996395746203316 996 $aThe historie of wyates rebellion$92348036 997 $aUNISA LEADER 05278nam 2200649Ia 450 001 9910144134303321 005 20170815115756.0 010 $a1-281-76689-5 010 $a9786611766894 010 $a0-470-38597-9 010 $a0-470-38596-0 035 $a(CKB)1000000000539712 035 $a(EBL)362085 035 $a(OCoLC)437224689 035 $a(SSID)ssj0000216109 035 $a(PQKBManifestationID)12077553 035 $a(PQKBTitleCode)TC0000216109 035 $a(PQKBWorkID)10194205 035 $a(PQKB)10604623 035 $a(MiAaPQ)EBC362085 035 $a(EXLCZ)991000000000539712 100 $a20080204d2008 uy 0 101 0 $aeng 135 $aur|n|---||||| 181 $ctxt 182 $cc 183 $acr 200 10$aOrganic synthesis$b[electronic resource] $estate of the art 2005-2007 /$fDouglass F. Taber 210 $aHoboken, NJ $cWiley$dc2008 215 $a1 online resource (242 p.) 225 1 $aOrganic Synthesis: State of the Art ;$vv.2 300 $aIncludes index. 311 $a0-470-28849-3 327 $aOrganic Synthesis: State of the Art 2005-2007; Contents; Preface; 1. Synthesis of (-)- Littoralisone; 2. Enantiocontrolled Construction of Oxygenated and Animated Stereogenic Centers; 3. Catalytic Enantioselective Construction of Alkylated Stereogenic Centers; 4. Catalytic Enantioselective Aldol/Mannich Reactions Leading to Extended Arrays of Stereogenic Centers; 5. Alternative Strategies for the Construction of Extended Arrays of Stereogenic Centers; 6. Synthesis of(-)- Avrainvillamide and (+)- Stephacidin B; 7. Best Synthetic Methods: Oxidation; 8. Best Synthetic Methods: Reduction 327 $a9. Selective Reactions of Alkenes10. Synthesis of the Potent FBBP12 Ligand Antascomicin B; 11. Best Synthetic Methods: Carbon-Carbon Bond Formation; 12. Enantioselective Construction of Quaternary Centers; 13. Pd-Mediated Arylation of Aromatic and Hetero Aromatic Rings; 14. The Overman Route to Gelsemine; 15. Stereoselective Construction of Oxygen Heterocycles; 16. Enantioselective Construction of Naturally-Occurring Cyclic Ethers; 17. Stereoselective Construction of Nitrogen Heterocycles; 18. The Stork Synthesis of (-)- Reserpine 327 $a19. Stereocontrolled Construction of Azacyclic Natural Products20. Preparation of Benzene Derivatives; 21. Preparation of Heteroaromatics; 22. Preparation and Reactions of Carboxylic Acids, Esters and Amides; 23. The Boger Route to (-)-Vindoline; 24. Protection of C-O and C-N; 25. New Catalysts and Strategies for Alkene Metathesis; 26. Creative Applications of Alkene and Alkyne Metathesis in Total Synthesis: (+)-8-epi-Xanthatin, (+)-Longicin, Latrunculin A, and Garsubellin A; 27. Synthesis of Erythronolide A; 28. Best Synthetic Methods: C-C Bond Formation 327 $a29. Catalytic Enantioselective Homologation of Aldehydes to Alcohols and Amines30. Catalytic Enantioselective Construction of Alkylated Stereogenic Centers; 31. Enantioselective Construction of Arrays of Stereogenic Centers; 32. Adventures in Complex Indole Synthesis: (-)-Fischerindole I, (+)-Fischerindole G and (+)-Weltwitindolinone A; 33. New Dienes and Dienophiles for Intermolecular and Intramolecular Diels-Alder Cycloaddtions; 34. Organocatalytic Preparation of Enantiomerically-Pure Carbocycles; 35. Carbocycle Construction by the Opening of Strained Rings: Synthesis of Tremulenolide A 327 $a36. The Corey Route to the Dolabellanes: Isoedunol and ?-Araneosene37. Transition-Metal Catalyzed Enantioselective Ring Construction; 38. Best Synthetic Methods: Functional Group Transformation; 39. Selective Reactions of Alkenes; 40. Synthesis and Absolute Stereochemical Assignment of (-)-Galbulimima Alkaloid 13; 41. Preparation of Benzene Derivatives; 42. Preparation of Heteroaromatic Derivatives; 43. Functional Group Transformation; 44. Functional Group Protection; 45. The Leighton Synthesis of Dolabelide D; 46. Stereocontrolled Construction of N-Heterocycles 327 $a47. Stereocontrolled Construction of O-Heterocycles 330 $aThe second volume in a series, Organic Synthesis: State of the Art 2005-2007 will provide you with a convenient, compact summary of the state of the art of organic synthesis. This reference guide will quickly lead you to the most important recent developments like how scientists can now prepare ketones by directly combining aldehydes with terminal alkenes. Inside, you will find detailed analysis of more than twenty total syntheses, including the Davies Synthesis of (-)-Colombiasin A and (-)-Elisapterosin B, the Overman Synthesis of (-)-Sarain A, and the Sorensen Synthesis of (-)-Guanaca 410 0$aOrganic Synthesis: State of the Art 606 $aOrganic compounds$xSynthesis 606 $aOrganic compounds$xSynthesis$xResearch 608 $aElectronic books. 615 0$aOrganic compounds$xSynthesis. 615 0$aOrganic compounds$xSynthesis$xResearch. 676 $a547.2 686 $aCHE 620f$2stub 686 $aVK 5500$2rvk 700 $aTaber$b D. F$g(Douglass F.),$f1948-$092850 801 0$bMiAaPQ 801 1$bMiAaPQ 801 2$bMiAaPQ 906 $aBOOK 912 $a9910144134303321 996 $aOrganic synthesis$91929231 997 $aUNINA