1,3-Dipolar Cycloaddition between Hetaryl Nitrones and Methyl Acrylate: Theoretical Study and Application to the Synthesis of Functionalized Pyrrolidines
Authors:
- Pedro MerinoPMPedro Merino
- Sonia AnoroSASonia Anoro
- Francisco MerchanFMFrancisco Merchan
- Tomas TejeroTTTomas Tejero
- 1 January 2000
- journal article
- Published by CLOCKSS Archive in HETEROCYCLES
- Vol. 53 (4) , 861
Abstract
No abstract availableKeywords
This publication has 12 references indexed in Scilit:
- Synthesis of nectrisine and related compounds, and their biological evaluationTetrahedron, 1999
- Stereoselective synthesis of alexine stereoisomers from (S)-pyroglutamic acidTetrahedron, 1998
- Practical synthesis of Boc and Fmoc protected 4-fluoro and 4-difluoroprolines from trans-4-hydroxyprolineTetrahedron Letters, 1998
- Formation and reduction reactions of 3-indo-3-yl-isoxazolidinesTetrahedron, 1997
- Pyrrole, pyrrolidine pyridine, piperidine, azepine and tropane alkaloidsNatural Product Reports, 1997
- Total synthesis of both enantiomers of trans-2,3-cis-3,4-dihydroxyprolineTetrahedron: Asymmetry, 1996
- Enantiospecific and Stereoselective Synthesis of Polyhydroxylated Pyrrolidines and Indolizidines from trans-4-Hydroxy-l-prolineThe Journal of Organic Chemistry, 1996
- Highly chemoselective reduction of N-Boc protected lactamsTetrahedron Letters, 1994
- Aromatic solvent-induced shifts in the 1H-NMR spectra of nitronesTetrahedron, 1992
- Origin of reactivity, regioselectivity, and periselectivity in 1,3-dipolar cycloadditionsJournal of the American Chemical Society, 1973