Solid-Phase Iminium Cyclization Reactions for the Synthesis of Natural Product-Like Diketopiperazines

Chemistry

• Cyclization Reaction 100%
• Occurrence in Nature 100%
• Glyoxylic Acid 100%
• Oxidative Elimination Reaction 100%
• Pictet-Spengler Synthesis 100%
• Ethyl Glyoxylate 100%
• Amino Acid 100%
• Alkaline Condition 50%
• Acrylamide 50%
• Acetamide 50%
• 2,5-diketopiperazines 50%
• Dihydroxylation 50%
• Hydroxamic Acid 50%
• Diastereoisomeric Mixture 50%
• Structure 50%
• Reverse Phase High Performance Liquid Chromatography 50%
• Furan 50%
• Thiophene 50%
• Serine 50%
• Proline 50%

Keyphrases

• Glyoxylamides 66%
• Pictet-Spengler Cyclization 66%
• Ethyl Glyoxylate 66%
• Glyoxylic Acid 66%
• Oxidative Cleavage 66%
• Homoprolines 33%
• Tetrasubstituted Furans 33%
• Exchange Pathways 33%
• Stereochemical Control 33%
• Glycolamide 33%
• Stereodifferentiation 33%
• Diketopiperazine Formation 33%
• Olefines 33%
• Substituted Thiophenes 33%
• 2,5-diketopiperazine 33%
• N-terminal Peptide 33%
• Acetamide 33%