|
[01] Dick's Encyclopedia of Practical Recipes and Processes, entry 4279 (1872) [02] Thorpe's Dictionary of Applied Chemistry Dick's Encyclopedia of Practical Recipes and Processes, entry 4271 (1872) [03] Chattaway, The Preparation of Allyl Alcohol, Journal of the Chemical Society 107, 407 (1915) Thorpe's Dictionary of Applied Chemistry [04] Chattaway, The Preparation of Allyl Alcohol, Journal of the Chemical Society 107, 407 (1915) Kamm and Marvel, Allyl Alcohol, Org. Syntheses Collective Vol. 1, p. 42 [05] Brauer, Handbook of Preparative Inorganic Chemistry, Vol 1, p. 285 [06] Brauer, Handbook of Preparative Inorganic Chemistry, Vol 1, p. 281-282 [07] Brauer, Handbook of Preparative Inorganic Chemistry, Vol 1, p. 287 [08] Brauer, Handbook of Preparative Inorganic Chemistry, Vol 1, p. 272-273 [09] Organic Reactions, Vol 3, p. 110-113 and 132-135 Organic Functional Group Preparations, Anhydrides. [10] Phelps, American Journal of Science, Vol 174 (Part 4, Vol 24), p 429-432 (1907) Organic Syntheses Collective Vol. 1, p 3-4 [11] Power and Kleber, Pharmaceutical Review, 101-103 (1896) [12] Chemical Abstracts 45, 3618i (1951) [13] Soap, Perfumery and Cosmetics 18, 404 (1945) Chemical Abstracts 39, 38804 [14] Chemical Abstracts 33, 65803; Ibid, 5637h (1953); Ibid, 47, 11656a; Ibid, 46, 4175e; Ibid, 44, 6579d [15] Perkin and Trikojus, Journal of the Chemical Society 1663-1666 (1927) [16] M. P. Gerchuk and V. M. Ivanova, Khim. Nauka i Prom. 3, 685-687 (1958) Chemical Abstracts 7094h (1959) [17] Bonthrone and Conforth, Journal of the Chemical Society (C) 1202-1204 (1969) [18] Feugaes, Bull. Soc. Chim. France Vol 61, 1892-1895 (1964) Chemical Abstracts 16001a (1964) [19] L. Bert, Compt. Rend. 213, 873-874 (1941) Chemical Abstracts 37, p 40606 (1941) [20] S. G. Mel'kanovitskaya and I. P. Tsukervanik, Dokl. Akad, Nauk USSR 8, 50-53 (1961) Chemical Abstracts 56, 14139e (1962) Mel'kanovitskaya and I. P. Tsukervanik, Uzbeksk. Khim. Zh. 9, 29-35 (1965) Chemical Abstracts 64, 1990g (1965) [21] E. Merck, German Patent 274,350 (12/24/1912) Chemical Abstracts 8, 3350 (1914) [22] Bienicki and Krajewski, Acta Polon. Pharm, 17, 421-425 (1960) (In Polish) Chemical Abstracts 14350e (1961) [23] Sakakibara, J. Chem. Soc. Japan 73, 235-236 (1952) Chemical Abstracts 47, 10511e (1953) [24] Mueller et al, US Patent 2,456,443 (1948) Chemical Abstracts 43, 7047e (1949) [25] H. E. Carter, Journal of Biological Chemistry 108, 619-632 (1935) [26] Pappas et al, Tetrahedron Letters 36, 4273-4278 (1966) Chemical Abstracts 65, 16890g (1966) [27] Nagai, J. Chem. Ind. Tokyo 23, 56-79 (1920) Chemical Abstracts 14, 2839 (1920) [28] K. Hirao et al, Tetrahedron 30, 2301-2305 (1974) [29] C. Graebe and E. Martz, Ber. 36, 1031 (1903) [30] R. Lange Journal of Organic Chemistry 27, 2037 (1962) [31] Pearl and Beyer, Journal of the American Chemical Society, 75, 2630 (1953) [32] Hayashi and Namura, Nippon Mokuzai Gakkaishi 13, 24-27 (1967) (In English) Chemical Abstracts 67, 45000z (1967) [33] Waterman and Preister, Rec. Trav. Chim. 47, 1027-1030 (1928) Chemical Abstracts 23, 1123 (1929) [34] Fugisawa and Deguchi, J. Pharm. Soc. Japan 74, 975-977 (1954) Chemical Abstracts 49, 10958i (1955) [35] Hoffsommer et al, US Patent 3,028,398 (1962) Chemical Abstracts 57, 9747c (1962) [36] Biniecki et al, Acta Polon. Pharm, 19, 31-35 (1962) Chemical Abstracts 58, 3334f (1963) US Patent 2,644,822 (1953) Chemical Abstracts 48, 6468h (1954) [37] Yuki et al, Japanese Patent 69:10,776 Chemical Abstracts 71, 30220e (1969) [38] Elks and Hey, Journal of the Chemical Society (London), p15-16 (1943) Chemical Abstracts 37, 19957 [39] Hinkley and Budavari, France Patent 1,450,200 (1966) Chemical Abstracts 66, 104825b (1967) [40] Auterhoff and Roth, Angewandte Chemie 67, 426-427 (1955) Chemical Abstracts 50, 4826c (1956) [41] C. R. Hauser and W. B. Renferrow, Journal of Chemical Education, 14, 542-544 (1937). [42] Shulgin and Braun, Journal of Pharmaceutical Sciences, 69, 192-195 (1980). [43] Nichols et al, J. Med. Chem., 29, 2009-2015 (1986). [44] Ann and Alexander Shulgin, PiHKAL, A Chemical Love Story, p 714 (1991). [45] Gairaud and Lappin, Journal of the Chemical Society, p 1-3 (1953). [46] G. A. Alles, Journal of the American Chemical Society p 271-274 (1932). Pharmaceutical Manufacturing Encyclopedia, p 82. [47] Austrian Patent 174,057 Feb 25 (1953) [48] Crossley and Moore, Studies on the Leuckart Reaction, J. Org. Chem., p 529-536 (1944). [49] Elks and Hey, 3,4-Methylenedioxyphenylisopropylamine, J. Chem. Soc., p15-16 (1942). [50] Ritter and Kalish, A New Reaction of Nitriles, J. Am. Chem. Soc. 70, 4048-4050 (1948). [51] Bienicki and Krajewski, Acta Polon. Pharm, 17, 421-425 (1960) (In Polish) Chemical Abstracts 55, 14350e (1961) [52] Ide and Buck, Journal of the American Chemical Society 62, 425-428 (1940) [53] Woodruff et al, Journal of the American Chemical Society 62, 922-924 (1940) [54] E. F. Kiefer, Journal of Medicinal Chemistry 15, 214 (1972) [55] Braun and Shulgin, Journal of Pharmaceutical Sciences 69, 192-195 (1980) [56] Nichols et al, Journal of Medicinal Chemistry 29, 2009-2015 (1986) [57] Crossley and Moore Studies on the Leuckart Reaction, Journal of Organic Chemistry 529-536 (1944) [58] Uncle Fester, Secrets of Methamphetamine Manufacture, 3rd Ed, Loompanics (1994) Novelli, Journal of the American Chemical Society 61, 520 (1939) [59] Journal of the American Chemical Society 53, 1879 (1931) [60] The Basidiomycete, Vol 1, #12 [61] Brauer, Handbook of Preparative Inorganic Chemistry, p 469 [62] Adams and Brown, Hydrazine Sulfate, Organic Syntheses Collective Volume I, p 309, Brauer, Handbook of Preparative Inorganic Chemistry, p 468. [63] Harborne et al, Phytochemistry, vol 8, 1729-1732 (1969). [64] Chemical Abstracts, vol 44, 5876e (1950) Chemical Abstracts, vol 44, 5877d (1950) [65] Chemical Abstracts, vol 60, 13091d (1950); Acta Polon Pharm, vol 19, 383-94 (1962). [66] Journal of the Chemical Society 151(2), 2303-2307 (1948). [67] Philip Catalfomo, The production of psilocybin in submerged culture by Psilocybe cubensis, University Microfilms (Ann Arbor, Michigan) order No. 63-7682, 294 pgs.; Dissertation Abstracts, 24, 953-4 (1963). Underground Psychedelic Library, The Psilocybin Producers Guide. |