By Maurice Shamma
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Additional resources for Isoquinoline Alkaloids Research 1972–1977
For a thorough discussion of the synthesis of 4-oxy- and 4-ketotetrahydroisoquinolines, see J. M. Bobbitt, Adv. Heterocycl. , 15, 99 (1973). 20. S. Teitel, J. O'Brien, and A. Brossi, J. Med. , 15, 845 (1972). For a compilation of the NMR spectra of monophenolic tetrahydroisoquinoline salts, see F. Schenker, R. A. Schmidt, T. Williams, and A. Brossi, J. Heterocycl. , 8, 665 (1971). 21. S. Teitel, J. O'Brien, W. Pool, and A. Brossi, J. Med. , 17, 134 (1974). 22. A. Brossi, A. Focella, and S. Teitel, Helv.
60. W. E. McEwen and R. L. Cobb, Chem. , 55, 511 (1955). 61. F. D. Popp, Adv. Heterocycl. , 9, 1 (1968). 62. F. D. Popp, Heterocycles, 1, 165 (1973). 63. J. Knabe and A. Frie, Arch. , 306, 648 (1973). For a versatile new synthesis of Reissert compounds using an acid chloride and trimethylsilyl cyanide in methylene chloride, see S. Ruchirawat, N. Phadungkul, M. Chuankamnerdkarn, and C. Thebtaranonth, Heterocycles, 6, 43 (1977). 64. H. W. Gibson, F. D. Popp, and A. Catala, J. Heterocycl. , 1, 251 (1964).
Knabe, Arch. , 292, 416 (1959). 49. D. E. Schwartz and J. Rieder, Clin. Chim. Acta, 6, 453 (1971). 50. J. Arthur, F. de Silva, N. Strojny, and N. Munno, J. Pharm. , 62, 1066 (1973). 51. K. C. Agrawal, R. J. Cushley, S. R. Lipsky, J. R. Wheaton, and A. C. Sartorelli, J. Med. , 15, 192 (1972); and K. C. Agrawal, P. D. Mooney, and A. C. Sartorelli, J. Med. , 19, 970 (1976). 52. Y. Ogata and Y. Sawaki, J. Am. Chem. , 95, 4692 (1973). 53. H. Stamm and J. Hoenicke, Arch. , 307, 340 (1974). 54. O. Hoshino, K.