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0141878086
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The application of polymer-supported reagents and scavengers in organic chemistry has been amply reviewed, a selection includes
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The application of polymer-supported reagents and scavengers in organic chemistry has been amply reviewed, a selection includes: (a) Baxendale, I.R.; Lee, A.-L.; Ley, S.V. Microwave Assisted Organic Synthesis, 2005, 133;
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Baxendale, I.R.1
Lee, A.-L.2
Ley, S.V.3
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(c) Ley, S.V.; Baxendale, I.R.; Bream, R.N.; Jackson, P.S.; Leach, A.G.; Longbottom, D.A.; Nesi, M.; Scoff, J.S.; Storer, R.I.; Taylor, S.J. J. Chem. Soc. Perkin Trans. 1, 2000, 3815.
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Nesi, M.7
Scoff, J.S.8
Storer, R.I.9
Taylor, S.J.10
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4
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33746023358
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The application of microwaves in organic chemistry has been amply reviewed
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The application of microwaves in organic chemistry has been amply reviewed: (a) Kappe, C.O. Chimia, 2006, 60, 308;
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Chimia
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Kappe, C.O.1
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7
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Some recent examples include
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Some recent examples include: (a) Bhattacharyya, S. Mol. Div., 2005, 9, 253;
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Mol. Div.
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Bhattacharyya, S.1
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8
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(b) Baxendale, I.R.; Ley, S.V.; Martinelli, M. Tetrahedron, 2005, 61, 5323;
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Tetrahedron
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Baxendale, I.R.1
Ley, S.V.2
Martinelli, M.3
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9
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Tetrahedron Lett.
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Donati, D.1
Morelli, C.2
Taddei, M.3
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Org. Lett.
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Wang, Y.1
Miller, R.L.2
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Djuric, S.W.4
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(e) Petricci E.; Mugnaini C.; Radi, M.; Corelli, F.; Botta, M. J. Org. Chem., 2004, 69, 7880.
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(c) Singh, V.; Khurana, A.; Kaur, I.; Sapehiyia, V.; Kad, G.L.; Singh, J. J. Chem. Soc. Perkin Trans. 1, 2002, 1766;
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Green Chem.
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(e) Yin, W.; Ma, Y.; Xu, J.; Zhao, Y. J. Org. Chem., 2006, 71, 4312.
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(d) King, L.C.; McWirther, M.; Rowland, L.R. J. Am. Chem. Soc., 1948, 70, 239;
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Chumbhale, V.R.; Parahdy, S.A.; Anilkumar, M.; Kadam, S.T.; Bokade, V.V. Chem. Eng. Res. Des., 2005, 83, 75.
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(none of the products were actually isolated)
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(a) Bjørsvik, H.R.; Vedia Merinero, J.A.; Liguori, L. Tetrahedron Lett., 2004, 45, 8615 (none of the products were actually isolated);
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(b) Bjørsvik, H.R.; Liguori, L.; González, R.R.; Vedia Merinero, J.A. Tetrahedron Lett., 2002, 43, 4985.
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(d) Habermann, J.; Ley, S.V.; Scicinski, J.J.; Scott, J.S.; Smits, R.; Thomas, A.W. J. Chem. Soc. Perkin Trans. 1, 1999, 2425.
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This cyclisation is known in literature, generally mildly basic conditions are being used, e.g
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This cyclisation is known in literature, generally mildly basic conditions are being used, e.g. (a) Bellutti, F.; Rampa, A.; Piazza, L.; Bisi, A.; Gobbi, S.; Bartolini, M.; Andrisano, V.; Cavalli, A.; Recantini, M.; Valenti, P. J. Med. Chem., 2005, 48, 4444;
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38
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3042634221
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Murata, T.; Shimada M.; Kadono, H.; Sakakibara, S.; Yoshino, T.; Masuda, T.; Shimazaki M.; Shintani, T.; Fuchikami, K.; Bacon, K.B.; Ziegelbauer, K.B.; Lowinger, T.B. Bioorg. Med. Chem. Lett., 2005, 14, 4013.
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Fuchikami, K.9
Bacon, K.B.10
Ziegelbauer, K.B.11
Lowinger, T.B.12
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39
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33846681380
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note
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Commercial material from Aldrich, catalogue number 22,696-3.
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40
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33846690242
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note
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The technical grade ion exchanger was extensively washed with methanol and then dried i. vac.
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41
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33846684019
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note
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Commercial material from Fluka, catalogue number 21580.
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42
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22244483070
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A recent letter describes the microwave assisted Kröhnke pyridine synthesis, which is not to be confused with the reaction described in this letter
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A recent letter (Tu, S.; Li, T.; Shi, F.; Fang, F.; Zhu, S.; Wei, X.; Zong, Z. Chem. Lett., 2005, 34, 732) describes the microwave assisted Kröhnke pyridine synthesis, which is not to be confused with the reaction described in this letter.
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(2005)
Chem. Lett.
, vol.34
, pp. 732
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Tu, S.1
Li, T.2
Shi, F.3
Fang, F.4
Zhu, S.5
Wei, X.6
Zong, Z.7
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