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note
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Microwave-assisted solid-phase organic synthesis (MASPOS) is used here for the organic reactions of resin-bound substrates performed in solvent at defined temperature under microwave irradiation. Microwave-assisted organic synthesis with inorganic supports, dry media, or under solventless conditions falls into a different category.
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For reviews, see: (a) Nefzi, A.; Ostresh, J. M.; Houghten, R. A. Chem. Rev. 1997, 97, 449-472. (b) Franzén, R. G. J. Comb. Chem. 2000, 2, 195-214. (c) Krchňák, V.; Holladay, M. W. Chem. Rev. 2002, 102, 61-91. (d) Brase, S.; Gil, C.; Knepper, K. Biorg. Med. Chem. 2002, 10, 2415-2437.
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For reviews, see: (a) Nefzi, A.; Ostresh, J. M.; Houghten, R. A. Chem. Rev. 1997, 97, 449-472. (b) Franzén, R. G. J. Comb. Chem. 2000, 2, 195-214. (c) Krchňák, V.; Holladay, M. W. Chem. Rev. 2002, 102, 61-91. (d) Brase, S.; Gil, C.; Knepper, K. Biorg. Med. Chem. 2002, 10, 2415-2437.
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Krchňák, V.1
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For reviews, see: (a) Nefzi, A.; Ostresh, J. M.; Houghten, R. A. Chem. Rev. 1997, 97, 449-472. (b) Franzén, R. G. J. Comb. Chem. 2000, 2, 195-214. (c) Krchňák, V.; Holladay, M. W. Chem. Rev. 2002, 102, 61-91. (d) Brase, S.; Gil, C.; Knepper, K. Biorg. Med. Chem. 2002, 10, 2415-2437.
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Brase, S.1
Gil, C.2
Knepper, K.3
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55
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0033598320
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For solution synthesis, see: (a) Owa, T.; Yoshino, H.; Okauchi, T.; Yoshimatsu, K.; Ozawa, Y.; Sugi, N. H.; Nagasu, T.; Koyanagi, N.; Kitoh, K. J. Med. Chem. 1999, 42, 3789-3799. (b) Owa, T.; Okauchi, T.; Yoshimatsu, K.; Sugi, N. H.; Ozawa, Y.; Nagasu, T.; Koyanagi, N.; Okabe, T.; Kitoh, K.; Yoshino, H. Bioorg. Med. Chem. Lett. 2000, 10, 1223-1226.
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Owa, T.1
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Yoshimatsu, K.4
Ozawa, Y.5
Sugi, N.H.6
Nagasu, T.7
Koyanagi, N.8
Kitoh, K.9
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56
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0034608622
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For solution synthesis, see: (a) Owa, T.; Yoshino, H.; Okauchi, T.; Yoshimatsu, K.; Ozawa, Y.; Sugi, N. H.; Nagasu, T.; Koyanagi, N.; Kitoh, K. J. Med. Chem. 1999, 42, 3789-3799. (b) Owa, T.; Okauchi, T.; Yoshimatsu, K.; Sugi, N. H.; Ozawa, Y.; Nagasu, T.; Koyanagi, N.; Okabe, T.; Kitoh, K.; Yoshino, H. Bioorg. Med. Chem. Lett. 2000, 10, 1223-1226.
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Owa, T.1
Okauchi, T.2
Yoshimatsu, K.3
Sugi, N.H.4
Ozawa, Y.5
Nagasu, T.6
Koyanagi, N.7
Okabe, T.8
Kitoh, K.9
Yoshino, H.10
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57
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0013209248
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For a review on anticancer and antiviral sulfonamides, see: Scozzafava, A.; Owa, T.; Mastrolorenzo, A.; Supuran, C. T. Curr. Med. Chem. 2003, 10, 925-953.
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Scozzafava, A.1
Owa, T.2
Mastrolorenzo, A.3
Supuran, C.T.4
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58
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0037152335
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For solution synthesis, see: Dai, W.-M.; Sun, L.-P.; Guo, D.-S. Tetrahedron Lett. 2002, 43, 7699-7702.
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(2002)
Tetrahedron Lett.
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Dai, W.-M.1
Sun, L.-P.2
Guo, D.-S.3
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Dai, W.-M.; Guo, D.-S.; Sun, L.-P. Tetrahedron Lett. 2001, 42, 5275.
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Rodriguez, A. L.; Koradin, C.; Dohle, W.; Knochel, P. Angew. Chem., Int. Ed. 2000, 39, 2488-2490.
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Rodriguez, A.L.1
Koradin, C.2
Dohle, W.3
Knochel, P.4
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61
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Purification of the end product was carried out
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For reduction of 5-nitroindole on Wang resin, see: Tois, J.; Franzén, R.; Aitio, O.; Huikko, K.; Taskinen, J. Tetrahedron Lett. 2000, 41, 2443-2446. Purification of the end product was carried out.
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Tois, J.1
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Taskinen, J.5
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Sakamoto, T.6
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(a) Saulnier, M. G.; Frennesson, D. B.; Deshpande, M. S.; Vyas, D. M. Tetrahedron Lett. 1995, 36, 7841-7844.
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(b) Hiroya, K.; Itoh, S.; Ozawa, M.; Kanamori, Y.; Sakamoto, T. Tetrahedron Lett. 2002, 43, 1277-1280.
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Hiroya, K.1
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Sakamoto, T.5
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65
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0141512488
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note
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f tag cannot be archived after exposure to microwave if the tag vertically sits in a 2-mL process vial. The reason is not known. Photos of the reaction vials are found in the Supporting Information.
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66
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0141852845
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and references therein
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van Esseveldt, B. C. J.; van Delft, F. L.; de Gelder, R.; Rutjes, F. P. J. T. Org. Lett. 2003, 5, 1717-1720 and references therein.
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Van Esseveldt, B.C.J.1
Van Delft, F.L.2
De Gelder, R.3
Rutjes, F.P.J.T.4
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67
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0141847089
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note
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Decomposition of the resin at the reaction temperatures as high as 200°C was not observed. Also, see refs 6g,n and 7c,d.
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68
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note
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For a recent solid-phase indole synthesis with microwave irradiation, see ref 7e.
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