Microwave assisted organic synthesis-a review

1 Review 1.1 Overview 1.2 Solid-phase organic synthesis (SPOS) 1.3 Beyond conventional solid-phase organic synthesis 1.4 The review 1.5 Some definitions 1.6 Solid-supported reagents and scavengers 1.7 Multi-step use of solid-supported reagents and scavenging reagents 1.8 Conclusions and future perspective 2 Introduction to the tables 2.1 Organisation of tables (reagent and catalyst section) 2.2 Representative data entry (reagent and catalyst section) 2.3 Organisation of tables (scavenging agents section) 2.4 Representative data entry (scavenging agents section) 3 Tables of reagents and catalysts 4 Tables of scavengers 5 Other relevant reviews 5.1 Insoluble polymers 5.1.1 Structure and physical properties (insoluble polymers) 5.1.2 General (insoluble polymers) 5.1.3 Reactions (insoluble polymers) 5.1.4 Miscellaneous (insoluble polymers) 5.2 Soluble polymers 5.2.1 General (soluble polymers) 5.2.2 Reactions (soluble polymers) 5.3 Inorganic solids 5.3.1 Structure and physical properties (inorganic solids) 5.3.2 General (inorganic solids) 5.3.3 Reactions (inorganic solids) 5.3.4 Miscellaneous (inorganic solids) 5.4 Miscellaneous supports 5.4.1 Structure and physical properties (miscellaneous supports) 5.4.2 General (miscellaneous supports) 5.4.3 Reactions (miscellaneous supports) 5.4.4 Miscellaneous (miscellaneous supports) 5.5 Purification strategies 5.5.1 Various supports (purification strategies) 5.5.2 Insoluble polymers (purification strategies) 6 Acknowledgements 7 Abbreviations 8 References 1 Review

Multi-step organic synthesis using solid-supported reagents and scavengers: a new paradigm in chemical library generation

2.7. Redox Deprotections 221 3. Thiol Protecting Groups 223 4. Carboxy Protecting Groups 223 4.1. Protection 224 4.2. Deprotection 226 5. Carbonyl Protecting Groups 227 5.1. Acetals 227 5.1.1. Protection 227 5.1.2. Deprotection 231 5.2. Dithioacetals 233 5.2.1. Protection 233 5.2.2. Deprotection 235 5.3. 1,3-Oxathiolanes 237 5.4. 1,1-Diacetates (Acylals) 238 5.4.1. Protection 238 5.4.2. Deprotection 239 5.5. Nitrogenous Derivatives 240 5.5.1. Protection 240 5.5.2. Deprotection 241 6. Amino Protecting Groups 242 6.1. Protection 242 6.2. Deprotection 244 7. Concluding Remarks 246 8. Acknowledgments 246 9. Abbreviations 246 10. References 246

Protection (and deprotection) of functional groups in organic synthesis by heterogeneous catalysis.

Solvent-free Knoevenagel condensations and Michael additions in the solid state and in the melt with quantitative yield

http://dspace.nitrkl.ac.in/dspace/bitstream/2080/871/1/oxidation.pdf

Oxidation by permanganate: synthetic and mechanistic aspects

A Simple, Efficient, and Selective Method for Tetrahydropyranylation of Alcohols on a Solid Phase of Alumina Impregnated with Zinc Chloride

Surface-mediated solid phase reaction. Mukaiyama-Michael addition of silyl enol ethers to methyl vinyl ketone on the surface of alumina

Microwave Assisted Michael Addition of Cycloalkenones and Substituted Enones on the Surface of Alumina in Dry Media

An unusual regioselective anti-markovnikov hydration of alkenes with zinc borohydride on silica gel support

Surface-Mediated Solid Phase Reaction. IX. A Convenient Procedure for Aldol Reaction of Ketene Silyl Acetals with Aldehydes on the Solid Surface of Alumina

Manika Saha

Papers

A Simple, Efficient, and Selective Method for Tetrahydropyranylation of Alcohols on a Solid Phase of Alumina Impregnated with Zinc Chloride

Surface-mediated solid phase reaction. Mukaiyama-Michael addition of silyl enol ethers to methyl vinyl ketone on the surface of alumina

Microwave Assisted Michael Addition of Cycloalkenones and Substituted Enones on the Surface of Alumina in Dry Media

An unusual regioselective anti-markovnikov hydration of alkenes with zinc borohydride on silica gel support

Surface-Mediated Solid Phase Reaction. IX. A Convenient Procedure for Aldol Reaction of Ketene Silyl Acetals with Aldehydes on the Solid Surface of Alumina