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http://dx.doi.org/10.5012/bkcs.2010.31.10.2989

Solvent-free Zinc-catalyzed Amine N-Formylation  

Kim, Joong-Gon (Biotechnology Division, Hanwha Chemical R&D Center)
Jang, Doo-Ok (Department of Chemistry, Yonsei University)
Publication Information
Bulletin of the Korean Chemical Society / v.31, no.10, 2010 , pp. 2989-2991 More about this Journal
Keywords
Amine; Formylation; Formic acid; Zinc; Solvent-free;
Citations & Related Records
Times Cited By KSCI : 2  (Citation Analysis)
Times Cited By Web Of Science : 4  (Related Records In Web of Science)
Times Cited By SCOPUS : 4
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1 Ugi, I.; Fetzer, U.; Eholzer, U.; Knupfer, H.; Offerman, K. Angew. Chem., Int. Ed. Engl. 1965, 4, 472.   DOI
2 Qiu, P.; Persson, D.; Leygraf, C. J. Electrochem. Soc. 2009, 156, C441.   DOI   ScienceOn
3 Chung, B. Y.; Maeng, C. O.; Kim, Y. H. J. Korean Chem. Soc. 1982, 26, 43.
4 Duczek, W.; Deutsch, J.; Vieth, S.; Niclas, H.-J. Synthesis 1996, 37.
5 Reddy, P. G.; Kumar, G. D. K.; Baskaran, S. Tetrahedron Lett. 2000, 41, 9149.   DOI   ScienceOn
6 Desai, B.; Danks, T. N.; Wagner, G. Tetrahedron Lett. 2005, 955.
7 Kim, J.-G.; Jang, D. O. Tetrahedron Lett. 2009, 50, 2688.   DOI   ScienceOn
8 Kim, J.-G.; Jang, D. O. Synlett 2007, 2501.
9 Jang, D. O.; Moon, K. S.; Cho, D. H.; Kim, J.-G. Tetrahedron Lett. 2006, 47, 6063.   DOI   ScienceOn
10 Munbunjong, W.; Lee, E. H.; Chavasiri, W.; Jang, D. O. Tetrahedron Lett. 2005, 46, 8769.
11 Cho, D. H.; Jang, D. O. Tetrahedron Lett. 2004, 45, 2285.   DOI   ScienceOn
12 Cho, D. H.; Kim, J. G.; Jang, D. O. Bull. Korean Chem. Soc. 2003, 24, 155.   DOI   ScienceOn
13 Jang, D. O.; Cho, D. H. Synlett 2002, 631.
14 Mihara, M.; Nakai, T.; Iwai, T.; Ito, T.; Ohno, T.; Mizuno, T. Synlett 2010, 253.
15 Sarvari, M. H.; Sharghi, H. J. Org. Chem. 2004, 69, 6953.   DOI   ScienceOn
16 Chakraborti, A. K.; Gulhane, R. Tetrahedron Lett. 2003, 44, 6749.   DOI   ScienceOn
17 Chakraborti, A. K.; Gulhane, R. Chem. Commun. 2003, 1896.
18 Jung, S. H.; Ahn, J. H.; Park, S. K.; Choi, J.-K. Bull. Korean Chem. Soc. 2002, 23, 149.   DOI   ScienceOn
19 Floresheimer, A.; Kula, M. R. Monatsh. Chem. 1988, 119, 1323.   DOI
20 Kim, J.-G.; Jang, D. O. Synlett 2010, 1231.
21 Geiger, R.; Siedel, W. Chem. Ber. 1969, 102, 2487.   DOI
22 Chen, B.-C.; Bendarz, M. S.; Zhao, R.; Sundeen, J. E.; Chen, P.; Shen, Z.; Skoumbourdis, A. P.; Barrish, J. C. Tetrahedron Lett. 2000, 41, 5453.   DOI   ScienceOn
23 Kobayashi, K.; Nagato, S.; Kawakita, M.; Morikawa, O.; Konishi, H. Chem. Lett. 1995, 575.
24 Jackson, A.; Meth-Cohn, O. J. Chem. Soc., Chem. Commun. 1995, 1319.
25 Downie, I. M.; Earle, M. J.; Heaney, H.; Shuhaibar, K. F. Tetrahedron 1993, 49, 4015.   DOI   ScienceOn
26 Kobayashi, S.; Nishio, K. J. Org. Chem. 1994, 56, 6620.
27 Kobayashi, S.; Yasuda, M.; Hachiya, I. Chem. Lett. 1996, 407.
28 Green, T. W.; Wuts, P. G. M. Protective Groups in Organic Synthesis, 4th ed.; Wiley Interscience: New York, 2007.
29 Martinez, J.; Laur, J. Synthesis 1982, 979.
30 Waki, J.; Meinhofer, J. J. Org. Chem. 1977, 42, 2019.   DOI
31 Chen, F. M. F.; Benoiton, N. L. Synthesis 1979, 709.
32 Luca, L. D.; Giacomelli, G.; Porcheddu, A.; Salaris, M. Synlett 2004, 2570.
33 Das, B.; Krishnaiah, K.; Balasubramanyam, P.; Veeranjaneyulu, B.; Kumar, D. N. Tetrahedeon Lett. 2008, 49, 2225.   DOI   ScienceOn
34 Shekhar, A. C.; Kumar, A. R.; Sathaiah, G.; Paul, L.; Sridhar, M.; Rao, P. S. Tetrahedron Lett. 2009, 50, 7099.   DOI   ScienceOn
35 Hill, D. R.; Hsiao, C.-N.; Kurukulasuriya, R.; Wittenberger, S. J. Org. Lett. 2002, 4, 111.   DOI   ScienceOn
36 Hosseini-Sarvari, M.; Sharghi, H. J. Org. Chem. 2006, 71, 6652.   DOI   ScienceOn
37 Strazzolini, P.; Giumanini, A. G.; Cauci, S. Tetrahedron 1990, 46, 1081.   DOI   ScienceOn
38 Sheehan, J. C.; Yang, D. D. H. J. Am. Chem. Soc. 1958, 80, 1154.   DOI
39 Kisfaludy, L.; Otvos, L., Jr. Synthesis 1987, 510.