1.Introduction 2.Hydroxy Protecting Groups 2.1. Esters 2.1.1. Protection 2.1.2. Deprotection 2.2. Silyl Ethers 2.2.1. Protection 2.2.2. Deprotection 2.3. Alkoxyalkyl Ethers 2.3.1. Protection as THP Ethers 2.3.2. Protection as Other Alkoxyalkyl Ethers 2.3.3. Deprotection 2.4. Tosylates 2.5. Selective Protection of Polyfunctional Compounds 2.6. Selective Deprotection of Polyprotected Compounds 2.7. Redox Deprotections 3.Thiol Protecting Groups 4.Carboxy Protecting Groups 4.1. Protection 4.2. Deprotection 5.Carbonyl Protecting Groups 5.1. Acetals 5.1.1. Protection 5.1.2. Deprotection 5.2. Dithioacetals 5.2.1. Protection 5.2.2. Deprotection 5.3. 1,3-Oxathiolanes 5.4. 1,1-Diacetates (Acylals) 5.4.1. Protection 5.4.2. Deprotection 5.5. Nitrogenous Derivatives 5.5.1. Protection 5.5.2. Deprotection 6.Amino Protecting Groups 6.1. Protection 6.2. Deprotection 7.Concluding Remarks 8.Acknowledgments 9.Abbreviations 10.References
Protection (and Deprotection) of Functional Groups in Organic Synthesis by Heterogeneous Catalysis / G. Sartori; R. Ballini; F. Bigi; G. Bosica; R. Maggi; P. Righi. - In: CHEMICAL REVIEWS. - ISSN 0009-2665. - STAMPA. - 104:(2004), pp. 199-250. [10.1021/cr0200769]
Protection (and Deprotection) of Functional Groups in Organic Synthesis by Heterogeneous Catalysis
RIGHI, PAOLO
2004
Abstract
1.Introduction 2.Hydroxy Protecting Groups 2.1. Esters 2.1.1. Protection 2.1.2. Deprotection 2.2. Silyl Ethers 2.2.1. Protection 2.2.2. Deprotection 2.3. Alkoxyalkyl Ethers 2.3.1. Protection as THP Ethers 2.3.2. Protection as Other Alkoxyalkyl Ethers 2.3.3. Deprotection 2.4. Tosylates 2.5. Selective Protection of Polyfunctional Compounds 2.6. Selective Deprotection of Polyprotected Compounds 2.7. Redox Deprotections 3.Thiol Protecting Groups 4.Carboxy Protecting Groups 4.1. Protection 4.2. Deprotection 5.Carbonyl Protecting Groups 5.1. Acetals 5.1.1. Protection 5.1.2. Deprotection 5.2. Dithioacetals 5.2.1. Protection 5.2.2. Deprotection 5.3. 1,3-Oxathiolanes 5.4. 1,1-Diacetates (Acylals) 5.4.1. Protection 5.4.2. Deprotection 5.5. Nitrogenous Derivatives 5.5.1. Protection 5.5.2. Deprotection 6.Amino Protecting Groups 6.1. Protection 6.2. Deprotection 7.Concluding Remarks 8.Acknowledgments 9.Abbreviations 10.ReferencesI documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.