Peter G. M. Wuts

Greene's Protective Groups in Organic Synthesis

• Gebundenes Buch

Produktbeschreibung

An indispensable and comprehensive reference for synthetic organic or medicinal chemists, this book presents valuable material on the application of protective groups in organic chemistry, which is not easily found by casual searching. Each chapter is updated with new material published since the last edition, totalling over 2800 references. The new edition continues the tradition of Greene's as a useful guide for the organic chemist to plan, investigate, and carry out organic syntheses in an efficient manner; providing the most relevant and useful examples to illustrate each methodology.

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An 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: "An essential bible for the library or personal bookshelf of chemists performing complex synthesis." (CHOICE, May 2007) "...the most up-to-date compilation available...should be an integral part of all institutional libraries...it is also highly recommended that individuals...maintain their own copy..." (Journal of Medicinal Chemistry, March 8, 2007) "...continues to be a comprehensive guide to the techniques for the formation and cleavage of protective groups." (Journal of the American Chemical Society, January 31, 2007)

Produktdetails

• Verlag: Wiley & Sons
• Artikelnr. des Verlages: 1W118057480
• 5. Aufl.
• Seitenzahl: 1408
• Erscheinungstermin: 17. November 2014
• Englisch
• Abmessung: 241mm x 161mm x 58mm
• Gewicht: 1865g
• ISBN-13: 9781118057483
• ISBN-10: 1118057481
• Artikelnr.: 41248035

Autorenporträt

Peter G.M. Wuts is a Distinguished Scientist at Kalexsyn, Inc. in Kalamazoo, Michigan.

Inhaltsangabe

Preface to the Fifth Edition xi Preface to the Fourth Edition xiii Preface
to the Third Edition xv Preface to the Second Edition xvii Preface to the
First Edition xix Abbreviations xxi 1. The Role of Protective Groups in
Organic Synthesis 1 Properties of a Protective Group 1 Historical
Development 2 Development of New Protective Groups 2 Selection of a
Protective Group from This Book 4 Synthesis of Complex Substances: Two
Examples (As used in the Synthesis of Himastatin and Palytoxin) of the
Selection Introduction and Removal of Protective Groups 5 Synthesis of
Himastatin 5 Synthesis of Palytoxin Carboxylic Acid 9 2. Protection for the
Hydroxyl Group Including 12- and 13-Diols 17 Ethers 26 Substituted Methyl
Ethers 33 Substituted Ethyl Ethers 87 Methoxy-Substituted Benzyl Ethers 146
Silyl Ethers 201 Esters 271 Bisfluorous Chain-Type Propanoate (Bfp-OR)
Ester 307 Proximity-Assisted Deprotection for Ester Cleavage 329
Miscellaneous Esters 336 Sulfonates Sulfenates and Sulfinates as Protective
Groups for Alcohols 337 Carbonates 347 Carbamates 371 Protection for 12-
and 13-Diols 375 Monoprotection of Diols 375 Cyclic Acetals and Ketals 385
Chiral Ketones 446 Cyclic Orthoesters 447 Silyl Derivatives 456 Cyclic
Carbonates 465 Cyclic Boronates 468 3. Protection for Phenols and Catechols
472 Protection for Phenols 475 Ethers 475 Silyl Ethers 522 Esters 528
Carbonates 535 Carbamates 538 Phosphinates 540 Sulfonates 541 Protection
for Catechols (12-Dihydroxybenzenes) 545 Cyclic Acetals and Ketals 545
Cyclic Esters 551 Protection for 2-Hydroxybenzenethiols 552 4. Protection
for the Carbonyl Group 554 Acetals and Ketals 559 Acyclic Acetals and
Ketals 559 Cyclic Acetals and Ketals 576 Chiral Acetals and Ketals 611
Dithio Acetals and Ketals 615 Cyclic Dithio Acetals and Ketals 620 Monothio
Acetals and Ketals 644 Diseleno Acetals and Ketals 649 Miscellaneous
Derivatives 650 O-Substituted Cyanohydrins 650 Substituted Hydrazones 654
Oxime Derivatives 661 12-Adducts to Aldehydes and Ketones 669 Cyclic
Derivatives 674 Protection of the Carbonyl Group as Enolate Anions Enol
Ethers Enamines and Imines 676 Monoprotection of Dicarbonyl Compounds 679
Selective Protection of alpha- and ß-Diketones 679 Cyclic Ketals Monothio
and Dithio Ketals 684 5. Protection for the Carboxyl Group 686 Esters 692
General Preparation of Esters 692 General Cleavage of Esters 699
Transesterification 704 Enzymatically Cleavable Esters 711 Substituted
Methyl Esters 723 2-Substituted Ethyl Esters 739 26-Dialkylphenyl Esters
768 Substituted Benzyl Esters 775 Silyl Esters 792 Activated Esters 796
Miscellaneous Derivatives 799 Stannyl Esters 812 Amides and Hydrazides 812
Amides 820 Hydrazides 825 Protection of Sulfonic Acids 828 Protection of
Boronic Acids 831 6. Protection for the Thiol Group 837 Thioethers 841
S-Diphenylmethyl Substituted S-Diphenylmethyl and S-Triphenylmethyl
Thioethers 855 Substituted S-Methyl Derivatives: Monothio Dithio and
Aminothio Acetals 864 Substituted S-Ethyl Derivatives 875 Silyl Thioethers
880 Thioesters 881 Thiocarbonate Derivatives 883 Thiocarbamate Derivatives
885 Miscellaneous Derivatives 886 Unsymmetrical Disulfides 886 Sulfenyl
Derivatives 888 Protection for Dithiols: Dithio Acetals and Ketals 891
Protection for Sulfides 892 S-P Derivatives 893 Protection for the Amino
Thiol Group 894 7. Protection for the Amino Group 895 Carbamates 907
Substituted Ethyl Carbamates 921 Carbamates Cleaved by a 16-Elimination 977
Carbamates Cleaved by ß-Elimination 979 Photolytically Cleaved Carbamates
983 Miscellaneous Carbamates 987 Urea-Type Derivatives 989 Amides 990
Assisted Cleavage of Amides 1007 Bisprotection of Amines 1009 Special -Nh
Protective Groups 1025 N-Alkyl and N-Aryl Amines 1025 Imine Derivatives
1060 Enamine Derivatives 1069 Quaternary Ammonium Salts 1072 N-Heteroatom
Derivatives 1073 N-Metal Derivatives 1073 N-N Derivatives 1078 N-P
Derivatives 1083 N-Si Derivatives 1086 N-S Derivatives 1088 Protection of
Amino Alcohols 1116 Protection for Imidazoles Pyrroles Indoles and Other
Aromatic Heterocycles 1120 N-Sulfonyl Derivatives 1120 Carbamates 1124
N-Alkyl and N-Aryl Derivatives 1129 N-Trialkylsilylamines R2N-SiR03 1131
N-Allylamine CH2.CHCH2NR2 1131 N-Benzylamine (Bn-NR2) PhCH2-NR2 1132 Amino
Acetal Derivatives 1137 Amides 1141 Protection for the Amide -NH 1151
Protection for the Sulfonamide -NH 1182 8. Protection for the Alkyne -CH
1194 9. Protection for the Phosphate Group 1203 Some General Methods for
Phosphate Ester Formation 1209 Removal of Protective Groups from Phosphorus
1210 Alkyl Phosphates 1214 Phosphates Cleaved by Cyclodeesterification 1223
2-Substituted Ethyl Phosphates 1228 Haloethyl Phosphates 1236 Benzyl
Phosphates 1239 Phenyl Phosphates 1246 Photochemically Cleaved Phosphate
Protective Groups 1254 Amidates 1258 Miscellaneous Derivatives 1261 10.
Reactivities Reagents and Reactivity Charts 1263 Reactivities 1263 Reagents
1264 Reactivity Charts 1267 Reactivity Chart 1. Protection for Hydroxyl
Group: Ethers 1269 Reactivity Chart 2. Protection for Hydroxyl Group:
Esters 1274 Reactivity Chart 3. Protection for 12- and 13-Diols 1278
Reactivity Chart 4. Protection for Phenols and Catechols 1282 Reactivity
Chart 5. Protection for the Carbonyl Group 1286 Reactivity Chart 6.
Protection for the Carboxyl Group 1290 Reactivity Chart 7. Protection for
the Thiol Group 1294 Reactivity Chart 8. Protection for the Amino Group:
Carbamates 1298 Reactivity Chart 9. Protection for the Amino Group: Amides
1302 Reactivity Chart 10. Protection for the Amino Group: Special -NH
Protective Groups 1306 Reactivity Chart 11. Selective Deprotection of Silyl
Ethers 1311 Index 1333