Highly Efficient and Stereoselective Radical Addition of Tertiary Amines to Electron-Deficient Alkenes − Application to the Enantioselective Synthesis of Necine Bases
- 1 June 2000
- journal article
- research article
- Published by Wiley in European Journal of Organic Chemistry
- Vol. 2000 (12) , 2227-2238
- https://doi.org/10.1002/1099-0690(200006)2000:12<2227::aid-ejoc2227>3.0.co;2-8
Abstract
No abstract availableKeywords
This publication has 45 references indexed in Scilit:
- α-C−H Bond Dissociation Energies of Some Tertiary AminesThe Journal of Organic Chemistry, 1998
- C−H Bond Dissociation Energies of Alkyl Amines: Radical Structures and Stabilization EnergiesJournal of the American Chemical Society, 1997
- 1-Amino- and 1-Amidoalkyl Radicals: Generation and Stereoselective ReactionsSynthesis, 1996
- Excited state processes in polymerization photoinitiatorsProgress in Organic Coatings, 1995
- Thiazolidine derivatives: A new source of α-aminoalkyl radicals for carbon-carbon bond formation in synthesisTetrahedron Letters, 1991
- Synthesis of cyclic α-amino acids through ring closure of glycine derived free radicalsTetrahedron Letters, 1990
- The Design and Application of Free Radical Chain Reactions in Organic Synthesis. Part 1Synthesis, 1988
- Substituent effects on 2-aza-5-hexynyl radical cyclization regiochemistryTetrahedron Letters, 1982
- Free-radical annelation in the synthesis of bicyclic β-lactams. 2. Alternative use of chloro-, phenylseleno-, and phenylthio-functionalities as free-radical precursorsTetrahedron Letters, 1981
- Free Radical Additions of Amines to Olefins1Journal of the American Chemical Society, 1958