| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5229779 | Tetrahedron | 2007 | 29 Pages |
Abstract
A detailed discussion on the application of [3+2] dipolar cycloaddition reactions in targeted syntheses is presented.
Keywords
InocTFANCSIACnAChRBOCDMFPFBTBAttBuAzomethine ylideMVKm-CPBAN-chlorosuccinimideCAL-BAzomethine iminetertiary butylIDCTBSRCMTBAFDMAP4-dimethylaminopyridineLSDTHF1,3-dipole1,4-diazabicyclo[2.2.2]octaneDMSOAqueousAzideAlkaloidethylAcetylTrifluoroacetic acidLysergic acid diethylamidemeta-Chloroperoxybenzoic acidNitrile oxideBetaineTetrabutylammonium fluorideTetrahydrofuranLDATosylRing-closing metathesisDABCOdimethyl formamideDiisobutylaluminum hydrideDIBALHDimethyl sulfoxideNatural product synthesisIntramolecular 1,3-dipolar cycloadditionIntramolecular dipolar cycloadditionLithium diisopropylamideMEMMethyl vinyl ketonemesylNitroneIncHuisgen reactionCarbonyl ylidenicotinic acetylcholine receptor
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Vijay Nair, T.D. Suja,