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Syntheses of Biologically Active 2-Arylcyclopropylamines
- Source :
- Synthesis. 49:1131-1149
- Publication Year :
- 2017
- Publisher :
- Georg Thieme Verlag KG, 2017.
-
Abstract
- The 2-arylcyclopropylamine (ACPA) motif is often seen in biologically active compounds. This review focuses on the synthesis of biologically active ACPAs and categorizes, by reaction type, the synthetic methods used toward such compounds. 1 Introduction 2 Cyclopropanation Using Diazo Compounds 2.1 Styrene 2.2 Cinnamate 2.3 Vinyl Phthalimide 2.4 Vinyl Acetamide 2.5 Oxazolone 2.6 Diketopiperazine 3 Cyclopropanation Using Ylides 3.1 Cinnamate 3.2 Nitrostyrene 3.3 Oxirane 3.4 Nitroacetate 4 Transformation of Cyclopropanes 4.1 Iodocyclopropane 4.2 Aminocyclopropane 5 Miscellaneous Methods 5.1 Kulinkovich Reaction 5.2 Three-Component Reaction 5.3 Intramolecular Nucleophilic Cyclization 5.4 Intramolecular Mitsunobu Reaction 5.5 Rearrangement from Cyclobutanone 6 Summary
- Subjects :
- 010405 organic chemistry
Organic Chemistry
Cyclobutanone
Biological activity
Reaction type
010402 general chemistry
01 natural sciences
Combinatorial chemistry
Catalysis
0104 chemical sciences
Phthalimide
chemistry.chemical_compound
chemistry
Nucleophile
Organic chemistry
Diazo
Mitsunobu reaction
Acetamide
Subjects
Details
- ISSN :
- 1437210X and 00397881
- Volume :
- 49
- Database :
- OpenAIRE
- Journal :
- Synthesis
- Accession number :
- edsair.doi...........f3e393d441dd2386121f2942b66efaa4