References
- Posner, G. H. An Introduction to Synthesis Using Organocopper Reagents; Wiley-Interscience: New York, 1980.
- Taylor, R. J. K. Organocopper Reagents; Oxford University Press: Oxford, 1994.
- Taylor, R. J. K. Synthesis 1985, 364.
- Perlmutter, P. Conjugate Addition Reactions in Organic Synthesis; Pergamon Press: Oxford, 1992.
- Hulce, M. Org. React. 1990, 38, 225.
- Lipshutz, B. H.; Sengupta, S. Org. React. 1992, 41, 135.
- Kozikowski, A. P.; Jung, S. H. J. Org. Chem. 1986, 51, 3400. https://doi.org/10.1021/jo00367a040
- Kozikowski, A. P.; Jung, S. H. Tetrahedron Lett. 1986, 27, 3227. https://doi.org/10.1016/S0040-4039(00)84760-7
- Kim, S.; Lee, P. H. Tetrahedron Lett. 1988, 29, 5413. https://doi.org/10.1016/S0040-4039(00)82882-8
- Kim, S.; Lee, P. H.; Kim, S. S.; Bull. Korean Chem. Soc. 1989, 10, 218.
- Kim, S.; Kim, Y. G.; Park, J. H. Tetrahedron Lett. 1991, 32, 2043. https://doi.org/10.1016/S0040-4039(00)78903-9
- Kim, S.; Park, J. H.; Kim, Y. G.; Lee, J. M. J. Chem. Soc., Chem. Commun. 1993, 1188.
- Kim, S.; Lee, B. S.; Park, J. H. Bull. Korean Chem. Soc. 1993, 14, 654.
- Lee, P. H.; Kim, S. Bull. Korean Chem. Soc. 1992, 13, 580.
- Lee, P. H.; Cho, M.; Han, I.-S.; Kim, S. Tetrahedron Lett. 1999, 40, 6975. https://doi.org/10.1016/S0040-4039(99)01438-0
- Jung, S. H.; Kim, J. H. Bull. Korean Chem. Soc. 2002, 23, 365. https://doi.org/10.5012/bkcs.2002.23.3.365
- Jung, S. H.; Kim, J. H. Bull. Korean Chem. Soc. 2002, 23, 1375. https://doi.org/10.5012/bkcs.2002.23.10.1375
- Jung, S. H.; Kim, J. H.; Kim, H. J. Bull. Korean Chem. Soc. 2004, 24, 136.
- Paternotte, I.; Fan, H. J.; Screve, P.; Cllaesen, M.; Tulkens, P. M.; Sonveaux, E. Bioorg. Med. Chem. 2001, 9, 493. https://doi.org/10.1016/S0968-0896(00)00255-8
- Hedaya, E.; Theodoropulos, S. Tetrahedron 1968, 24, 2241. https://doi.org/10.1016/0040-4020(68)88126-8
Cited by
- Exocyclic Olefinic Maleimides: Synthesis and Application for Stable and Thiol-Selective Bioconjugation vol.128, pp.4, 2015, https://doi.org/10.1002/ange.201508118
- Exocyclic Olefinic Maleimides: Synthesis and Application for Stable and Thiol-Selective Bioconjugation vol.55, pp.4, 2015, https://doi.org/10.1002/anie.201508118
- A One-pot Green Synthesis of Alkylidenesuccinimides vol.29, pp.9, 2011, https://doi.org/10.1002/cjoc.201180332
- Facile Preparation of Alkylidenesuccinimides from Maleimides via the Phosphoniosilylation Process. vol.35, pp.52, 2004, https://doi.org/10.1002/chin.200452057
- A New Entry to β-Functionalization of Enones: Pentyloxy Group Incorporation in the TBSOTf-Mediated Ring-Opening Reaction of Epoxides with Ylides Derived from the Phosphoniosilylation Products of vol.35, pp.8, 2014, https://doi.org/10.5012/bkcs.2014.35.8.2573
- A Short‐Step Synthesis of 1,6‐Methano[10]annulene‐3,4‐dicarboximides and Their Benzene‐, Naphthalene‐, and Thiophene‐Annulated Compounds vol.2014, pp.27, 2004, https://doi.org/10.1002/ejoc.201402776
- Iterative Arylation of Itaconimides with Diazonium Salts through Electrophilic Palladium Catalysis: Divergent β-H-Elimination Pathways in Repetitive Matsuda-Heck Reactions vol.84, pp.9, 2019, https://doi.org/10.1021/acs.joc.9b00627