LEADER 05494nam 2200697 450 001 9910822567703321 005 20200520144314.0 010 $a1-118-90512-1 010 $a1-118-90507-5 010 $a1-118-90509-1 035 $a(CKB)3710000000218113 035 $a(EBL)1762794 035 $a(SSID)ssj0001288957 035 $a(PQKBManifestationID)11821475 035 $a(PQKBTitleCode)TC0001288957 035 $a(PQKBWorkID)11297375 035 $a(PQKB)11272164 035 $a(DLC) 2014012443 035 $a(Au-PeEL)EBL1762794 035 $a(CaPaEBR)ebr10906607 035 $a(CaONFJC)MIL635738 035 $a(PPN)183559924 035 $a(OCoLC)875056236 035 $a(MiAaPQ)EBC1762794 035 $a(EXLCZ)993710000000218113 100 $a20140818h20142014 uy 0 101 0 $aeng 135 $aur|n|---||||| 181 $ctxt 182 $cc 183 $acr 200 10$aGreene's protective groups in organic synthesis /$fPeter G. M. Wuts 205 $aFifth edition. 210 1$aHoboken, New Jersey :$cWiley,$d2014. 210 4$dİ2014 215 $a1 online resource (1399 p.) 300 $aIncludes index. 311 $a1-322-04487-2 311 $a1-118-05748-1 327 $aGreene's Protective Groups in Organic Synthesis; Contents; Preface to the Fifth Edition; Preface to the Fourth Edition; Preface to the Third Edition; Preface to the Second Edition; Preface to the First Edition; Abbreviations; 1. The Role of Protective Groups in Organic Synthesis; Properties of a Protective Group; Historical Development; Development of New Protective Groups; Selection of a Protective Group from This Book; Synthesis of Complex Substances: Two Examples (As used in the Synthesis of Himastatin and Palytoxin) of the Selection, Introduction, and Removal of Protective Groups 327 $aSynthesis of HimastatinSynthesis of Palytoxin Carboxylic Acid; 2. Protection for the Hydroxyl Group, Including 1,2- and 1,3-Diols; Ethers; Substituted Methyl Ethers; Substituted Ethyl Ethers; Methoxy-Substituted Benzyl Ethers; Silyl Ethers; Esters; Bisfluorous Chain-Type Propanoate (Bfp-OR) Ester; Proximity-Assisted Deprotection for Ester Cleavage; Miscellaneous Esters; Sulfonates, Sulfenates, and Sulfinates as Protective Groups for Alcohols; Carbonates; Carbamates; Protection for 1,2- and 1,3-Diols; Monoprotection of Diols; Cyclic Acetals and Ketals; Chiral Ketones; Cyclic Orthoesters 327 $aSilyl DerivativesCyclic Carbonates; Cyclic Boronates; 3. Protection for Phenols and Catechols; Protection for Phenols; Ethers; Silyl Ethers; Esters; Carbonates; Carbamates; Phosphinates; Sulfonates; Protection for Catechols (1,2-Dihydroxybenzenes); Cyclic Acetals and Ketals; Cyclic Esters; Protection for 2-Hydroxybenzenethiols; 4. Protection for the Carbonyl Group; Acetals and Ketals; Acyclic Acetals and Ketals; Cyclic Acetals and Ketals; Chiral Acetals and Ketals; Dithio Acetals and Ketals; Cyclic Dithio Acetals and Ketals; Monothio Acetals and Ketals; Diseleno Acetals and Ketals 327 $aMiscellaneous DerivativesO-Substituted Cyanohydrins; Substituted Hydrazones; Oxime Derivatives; 1,2-Adducts to Aldehydes and Ketones; Cyclic Derivatives; Protection of the Carbonyl Group as Enolate Anions, Enol Ethers, Enamines, and Imines; Monoprotection of Dicarbonyl Compounds; Selective Protection of ?- and ?-Diketones; Cyclic Ketals, Monothio and Dithio Ketals; 5. Protection for the Carboxyl Group; Esters; General Preparation of Esters; General Cleavage of Esters; Transesterification; Enzymatically Cleavable Esters; Substituted Methyl Esters; 2-Substituted Ethyl Esters 327 $a2,6-Dialkylphenyl EstersSubstituted Benzyl Esters; Silyl Esters; Activated Esters; Miscellaneous Derivatives; Stannyl Esters; Amides and Hydrazides; Amides; Hydrazides; Protection of Sulfonic Acids; Protection of Boronic Acids; 6. Protection for the Thiol Group; Thioethers; S-Diphenylmethyl, Substituted S-Diphenylmethyl, and S-Triphenylmethyl Thioethers; Substituted S-Methyl Derivatives: Monothio, Dithio, and Aminothio Acetals; Substituted S-Ethyl Derivatives; Silyl Thioethers; Thioesters; Thiocarbonate Derivatives; Thiocarbamate Derivatives; Miscellaneous Derivatives 327 $aUnsymmetrical Disulfides 330 $aAn indispensable reference for any practicing synthetic organic or medicinal chemist, this book continues the tradition of Greene's as comprehensive in the overall scope of coverage, providing the most relevant and useful examples to illustrate each methodology. Presents valuable material, on the application of protective groups in organic chemistry, that is not easily found by casual searching Helps chemists to plan, investigate, and carry out organic syntheses in an efficient manner Adds over 2800 new references to update since the publication of the last edition Reviews of the prior edition 606 $aOrganic compounds$xSynthesis 606 $aProtective groups (Chemistry) 615 0$aOrganic compounds$xSynthesis. 615 0$aProtective groups (Chemistry) 676 $a547.2 700 $aWuts$b Peter G. M.$091398 701 $aGreene$b Theodora W$g(Theodora Whatmough),$f1931-2005.$091370 701 $aGreene$b Theodora W$g(Theodora Whatmough),$f1931-2005.$091370 801 0$bMiAaPQ 801 1$bMiAaPQ 801 2$bMiAaPQ 906 $aBOOK 912 $a9910822567703321 996 $aGreene's protective groups in organic synthesis$94022566 997 $aUNINA