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85031219273
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For previous syntheses of thunberginol A (3a), see: (a) Ref. 13b. (b) Ref. 13d.
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48
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85031211760
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For previous syntheses of thunberginol A (3a), see: (a) Ref. 13b. (b) Ref. 13d.
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49
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85031224991
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For previous syntheses of thunberginol B (3b), see: Ref. 13b
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For previous syntheses of thunberginol B (3b), see: Ref. 13b.
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56
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(b) A short time after the publication of our paper in which we had described the synthesis of iodo derivatives of general formula 5 by iodolactonization of the corresponding methyl 2-(arylethynyl)benzoates 6 or 2-(arylethynyl)benzoic acids 7 (see: Ref. 21a), a communication was published in which it was reported the preparation of 3-substituted 4-iodoisocoumarins 5 from 2-(1-alkynyl)benzoates by a procedure very similar to one which we had previously described for the synthesis of iodides of general formula 5: Yao T., Larock R.C. Tetrahedron Lett. 43:2002;7401-7404. Two examples of synthesis of unsymmetrical 3,4-disubstituted isocoumarins were also reported in this communication.
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Roma, September 16-22; Atti P4
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For a preliminary communication on this subject, see: Carpita, A.; Stabile, P.; Mannina, L.; Rossi, R. Communication at the XXVIII Convegno Nazionale della Divisione di Chimica Organica, Roma, September 16-22, 2002; Atti P4.
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Carpita, A.1
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For the synthesis of 4-substituted isocoumarins with no substituent at the 3 position, see: (a) Kimura M., Waki I., Deguchi Y., Amemiya K., Maeda T. Chem. Pharm. Bull. 31:1983;1277-1282 (b) Belgaonkar V.H., Usgaonkar R.N. J. Chem. Soc., Perkin Trans. 1. 1977;702-706 (c) Arora P.K., Ray S. J. Indian Chem. Soc. LXII:1985;383-385 (d) Kim S., Fan G.-, Lee J., Lee J.J., Kim D. J. Org. Chem. 67:2002;3127-3130.
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For the synthesis of 4-substituted isocoumarins with no substituent at the 3 position, see: (a) Kimura M., Waki I., Deguchi Y., Amemiya K., Maeda T. Chem. Pharm. Bull. 31:1983;1277-1282 (b) Belgaonkar V.H., Usgaonkar R.N. J. Chem. Soc., Perkin Trans. 1. 1977;702-706 (c) Arora P.K., Ray S. J. Indian Chem. Soc. LXII:1985;383-385 (d) Kim S., Fan G.-, Lee J., Lee J.J., Kim D. J. Org. Chem. 67:2002;3127-3130.
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For the synthesis of 4-substituted isocoumarins with no substituent at the 3 position, see: (a) Kimura M., Waki I., Deguchi Y., Amemiya K., Maeda T. Chem. Pharm. Bull. 31:1983;1277-1282 (b) Belgaonkar V.H., Usgaonkar R.N. J. Chem. Soc., Perkin Trans. 1. 1977;702-706 (c) Arora P.K., Ray S. J. Indian Chem. Soc. LXII:1985;383-385 (d) Kim S., Fan G.-, Lee J., Lee J.J., Kim D. J. Org. Chem. 67:2002;3127-3130.
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For the synthesis of 4-substituted isocoumarins with no substituent at the 3 position, see: (a) Kimura M., Waki I., Deguchi Y., Amemiya K., Maeda T. Chem. Pharm. Bull. 31:1983;1277-1282 (b) Belgaonkar V.H., Usgaonkar R.N. J. Chem. Soc., Perkin Trans. 1. 1977;702-706 (c) Arora P.K., Ray S. J. Indian Chem. Soc. LXII:1985;383-385 (d) Kim S., Fan G.-, Lee J., Lee J.J., Kim D. J. Org. Chem. 67:2002;3127-3130.
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85031231388
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3 and Triton B: Ref. 15b
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3 and Triton B: Ref. 15b.
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0026947814
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Yoshikawa M., Uchida E., Chatani N., Murakami N., Yamahara. J. Chem. Pharm. Bull. 40:1992;3121-3123.
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66
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85031214119
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sp2-hybridized organic halide, see: Ref. 16d
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sp2-hybridized organic halide, see: Ref. 16d.
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67
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0000131734
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For other Stille-type reactions performed using catalyst sytems wich contain CuI, see: (a) Farina V., Krishnan B. J. Am. Chem. Soc. 113:1991;9585-9595 (b) Ref. 16d. (c) Ref. 16i. (d) Bellina F., Carpita A., Ciucci D., De Santis M., Rossi R. Tetrahedron. 49:1993;4677-4698 (e) Rossi R., Bellina F., Carpita A., Mazzarella F. Tetrahedron. 52:1996;4095-4110.
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85031216611
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Ref. 16d
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For other Stille-type reactions performed using catalyst sytems wich contain CuI, see: (a) Farina V., Krishnan B. J. Am. Chem. Soc. 113:1991;9585-9595 (b) Ref. 16d. (c) Ref. 16i. (d) Bellina F., Carpita A., Ciucci D., De Santis M., Rossi R. Tetrahedron. 49:1993;4677-4698 (e) Rossi R., Bellina F., Carpita A., Mazzarella F. Tetrahedron. 52:1996;4095-4110.
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69
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85031219246
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Ref. 16i
-
For other Stille-type reactions performed using catalyst sytems wich contain CuI, see: (a) Farina V., Krishnan B. J. Am. Chem. Soc. 113:1991;9585-9595 (b) Ref. 16d. (c) Ref. 16i. (d) Bellina F., Carpita A., Ciucci D., De Santis M., Rossi R. Tetrahedron. 49:1993;4677-4698 (e) Rossi R., Bellina F., Carpita A., Mazzarella F. Tetrahedron. 52:1996;4095-4110.
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70
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0027217418
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For other Stille-type reactions performed using catalyst sytems wich contain CuI, see: (a) Farina V., Krishnan B. J. Am. Chem. Soc. 113:1991;9585-9595 (b) Ref. 16d. (c) Ref. 16i. (d) Bellina F., Carpita A., Ciucci D., De Santis M., Rossi R. Tetrahedron. 49:1993;4677-4698 (e) Rossi R., Bellina F., Carpita A., Mazzarella F. Tetrahedron. 52:1996;4095-4110.
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For other Stille-type reactions performed using catalyst sytems wich contain CuI, see: (a) Farina V., Krishnan B. J. Am. Chem. Soc. 113:1991;9585-9595 (b) Ref. 16d. (c) Ref. 16i. (d) Bellina F., Carpita A., Ciucci D., De Santis M., Rossi R. Tetrahedron. 49:1993;4677-4698 (e) Rossi R., Bellina F., Carpita A., Mazzarella F. Tetrahedron. 52:1996;4095-4110.
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0035851248
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For another recent synthesis of (E)-3-ylidenephthalides, see:
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For another recent synthesis of (E)-3-ylidenephthalides, see: Mukhopadhay R., Kundu N.G. Tetrahedron. 57:2001;9475-9480.
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33748651297
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For previous syntheses of (Z)-3-ylidenephthalides, see: (a) Kundu N.G., Pal M., Nandi B. J. Chem. Soc., Perkin Trans. 1. 1998;561-568 (b) Mali R.S., Babu K.N. J. Org. Chem. 63:1998;2488-2492 (c) Mali R.S., Jagtap P.G. J. Chem. Res. (S). 1993;184-185 (d) Sashida H., Kawamukai A. J. Heterocycl. Chem. 35:1998;165-167.
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For previous syntheses of (Z)-3-ylidenephthalides, see: (a) Kundu N.G., Pal M., Nandi B. J. Chem. Soc., Perkin Trans. 1. 1998;561-568 (b) Mali R.S., Babu K.N. J. Org. Chem. 63:1998;2488-2492 (c) Mali R.S., Jagtap P.G. J. Chem. Res. (S). 1993;184-185 (d) Sashida H., Kawamukai A. J. Heterocycl. Chem. 35:1998;165-167.
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