References
- Synthesis;In Advances in Heterocyclic Chemistry v.591;42 Katritzky, A. R., Ed. Oediger, H.; Moller, F.; Eiter, K.;Hermecz, I.
- Tetrahedron;J. Chem.Soc. Chem. Commun.;J. Heterocycl. Chem.;J. Chem. Soc. Chem. Commun.;J. Org. Chem.;Tetrahedron v.50;325;30;46;38 Lammers, H.; Cohen-Fernandes, P.; Habraken, C. L.;Sutherland, J. K.;Perbost, M.; Lucas,M.; Chavis, C.; Imbach, J.-L.;Chambers, R. D.; Roche, A. J.; Batsanov, A.S.; Howard, J. A. K.;McCoy, L. L.; Mal, D.;Juneja, T. R.; Garg, D. K.; Schafer, W.
- Tetrahedron;Tetrahedron;In Organic Reactions v.44;52;51 Paquette, L. A., Ed. Drewes, S. E.; Roos, G. H. P.;Basavaiah, D.; Rao, P. D.; Hyma, R. S.;Ciganek, E.
- Tetrahedron Lett.;Org. Lett.;Tetrahedron Lett.;Tetrahedron Lett. v.42;2;39;42 Basavaiah, D.; Kumaragurubaran, N.; Sharada, D. S.;Yang, K.-S.; Chen, K.;Chamakh, A.; Amri, H.;Basavaiah, D.; Kumaragurubaran,N.
- Org. Lett.;Tetrahedron Lett.;Bull. Korean Chem. Soc.;Tetraherdon Lett.;Tetrahedron Lett. v.2;41;21;39;40 Kim, J. N.; Lee, K. Y.; Kim, H. S.; Kim, T. Y.;Kim, H. S.; Kim, T. Y.; Lee, K. Y.;Chung, Y. M.; Lee, H. J.; Kim, J. N.;Lee, H. J.; Chung, Y. M.; Lee, K. Y.;Kim, J. N.;Lee, H. J.; Seong, M. R.; Kim, J. N.;Lee, H. J.; Kim, H. S.; Kim, J. N.;
- Tetrahedron Lett. v.42 For the synthesis of 2-substituted naphthalenes from the Baylis-Hillman acetates Kim, J. N.; Im, Y. J.; Gong, J. H.;Lee, K. Y.
- Can. J. Chem. v.53 Deslongchamps.; Dube, S.; Lebteux, C.; Patterson, D. R.;Taillefer, R. J.
- The corresponding 1,2-dihydroquinoline derivative might be formed from the corresponding 2f-E. However, we cannot isolate it in pure state.
Cited by
- Nucleophilicities and carbon basicities of DBU and DBN vol.2008, pp.15, 2001, https://doi.org/10.1039/b801811a
- DBU-catalyzed three-component one-pot synthesis of highly functionalized pyridines in aqueous ethanol vol.46, pp.1, 2009, https://doi.org/10.1002/jhet.32
- DBU: a highly efficient catalyst for one-pot synthesis of substituted 3,4-dihydropyrano[3,2-c]chromenes, dihydropyrano[4,3-b]pyranes, 2-amino-4H-benzo[h]chromenes and 2-amino-4H benzo[g]chromenes in a vol.66, pp.30, 2001, https://doi.org/10.1016/j.tet.2010.05.082
- DBU‐Promoted Nucleophilic Activation of Carbonic Acid Diesters vol.2011, pp.13, 2011, https://doi.org/10.1002/ejoc.201001725
- Reactions of nitroxides XIII: Synthesis of the Morita–Baylis–Hillman adducts bearing a nitroxyl moiety using 4-acryloyloxy-2,2,6,6-tetramethylpiperidine-1-oxyl as a starting compound, an vol.8, pp.None, 2001, https://doi.org/10.3762/bjoc.8.171
- Pentacyclic coumarin-based blue emitters – the case of bifunctional nucleophilic behavior of amidines vol.50, pp.43, 2014, https://doi.org/10.1039/c4cc01106f
- Polyethylene glycol-bonded 1,8-diazabicyclo[5.4.0]undec-7-ene (PEG–DBU) as a surfactant-combined base catalyst for the application of nucleosides as reagents in multi-component syntheses of 8-su vol.17, pp.10, 2015, https://doi.org/10.1039/c5gc01448d
- p -Nitrophenyl carbonate promoted ring-opening reactions of DBU and DBN affording lactam carbamates vol.12, pp.None, 2001, https://doi.org/10.3762/bjoc.12.197
- One-Pot Transformation of Carbohydrates into Valuable Furan Derivatives via 5-Hydroxymethylfurfural vol.9, pp.22, 2001, https://doi.org/10.1002/cctc.201701106
- DBU: A Reaction Product Component vol.5, pp.37, 2001, https://doi.org/10.1002/slct.202002910