Aflatoxin total synthesis concerns the total synthesis of a group of organic compounds called aflatoxins. These compounds occur naturally in several fungi. As with other chemical compound targets in organic chemistry, the organic synthesis of aflatoxins serves various purposes. Traditionally it served to prove the structure of a complex biocompound in addition to evidence obtained from spectroscopy. It also demonstrates new concepts in organic chemistry (reagents, reaction types) and opens the way to molecular derivatives not found in nature. And for practical purposes, a synthetic biocompound is a commercial alternative to isolating the compound from natural resources. Aflatoxins in particular add another dimension because it is suspected that they have been mass-produced in the past from biological sources as part of a biological weapons program.[1][2]
The synthesis of racemic aflatoxin B1 has been reported by Buechi et al. in 1967[3] and that of racemic aflatoxin B2 by Roberts et al. in 1968[4] The group of Barry Trost of Stanford University is responsible for the enantioselective total synthesis of (+)-Aflatoxin B1 and B2a in 2003.[5] In 2005 the group of E. J. Corey of Harvard University presented the enantioselective synthesis of Aflatoxin B2.[6]
^Zilinskas, Raymond A. (1997). "Iraq's Biological Weapons. The Past as Future?". JAMA. 278 (5): 418–424. doi:10.1001/jama.1997.03550050080037.
^Venkataramana, M.; Chandranayaka, S.; Prakash, H. S.; Niranjana, S. R. (2015). "Mycotoxins Relevant to Biowarfare and Their Detection". In Gopalakrishnakone, P.; Balali-Mood, Mahdi; Llewellyn, Lyndon; Singh, Bal Ram (eds.). Biological Toxins and Bioterrorism. Springer. pp. 295–319. ISBN 978-94-007-5869-8.
^Buechi, George; Foulkes, D. M.; Kurono, Masayasu; Mitchell, Gary F.; Schneider, Richard Stephen (1967). "The total synthesis of racemic aflatoxin B1". Journal of the American Chemical Society. 89 (25): 6745–53. doi:10.1021/ja01001a062. PMID 6063661.
^Roberts, John C.; Sheppard, A. H.; Knight, J. A.; Roffey, Patrick (1968). "Studies in mycological chemistry. Part XXII. Total synthesis of (±)-aflatoxin-B2". Journal of the Chemical Society C: Organic. 1: 22–24. doi:10.1039/J39680000022. PMID 5688875.
^Trost, B. M.; Toste, F. D. "Palladium Catalyzed Kinetic and Dynamic Kinetic Asymmetric Transformations of γ-Acyloxybutenolides. Enantioselective Total Synthesis of (+)-Aflatoxin B1 and B2a". J. Am. Chem. Soc.2003, 125, 3090–3100. doi:10.1021/ja020988s
^Zhou, G.; Corey, E. J. "Short, Enantioselective Total Synthesis of Aflatoxin B2 Using an Asymmetric [3+2]-Cycloaddition Step". J. Am. Chem. Soc.2005, 127, 11958–11959. doi:10.1021/ja054503m
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