1. Chibo Honga, Gary L. Firestoneb and Leonard F. Bjeldanes. Bcl-2 family-mediated apoptotic effects of 3,3′-diindolylmethane (DIM) in human breast cancer cells. Biochemical Pharmacology, 2002, 63, 6, p. 1085-1097
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http://dx.doi.org/10.1016/S0006-2952(02)00856-0
2. D. Maciejewska, M. Niemyjska, I. Wolska, M. W\lostowski, and M. Rasztawicka. Synthesis, Spectroscopic Studies and Crystal Structure of 5,5'-Dimethoxy-3,3'-methanediyl-bis-indole as the Inhibitor of Cell Proliferation of Human Tumors. Z. Naturforsch., 2004, 59, 10, p. 1137-1142.
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http://www.znaturforsch.com/ab/v59b/c59b.htm#No10
3. Sergey V. Popil'nichenko, Vladimir S. Brovarets, Alexander N. Chernega, Denis V. Poltorak, Boris S. Drach. A facile synthesis of new thieno[2,3-b][1,4]thiazine derivatives starting from 2-acylamino-3,3-dichloroacrylonitriles. Heteroatom Chem., 2006, 17, 5, p. 411-415.
4. Kohji Suda and Toshikatsu Takanami. A Novel Electrochemical Oxidation Reactions Utilizing Cyclodextrins. Anodic Oxidation of Indole–Cyclodextrin–Alcohol System. Chem. Lett., 1994, 23, 10, p. 1915-1916
5. Samuel E. Watson and Anatoly Markovich. Synthesis of Protected 5-Formylpyrido[2,3-d]pyrimidine via a 2,3,4-Trisubstituted Pyridine Using an ortho-Lithiation Strategy; Application to the Synthesis of a Folate Derivative. Heterocycles, 1998, 48, 10, p. 2149-2155.
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https://www2.heterocycles.jp/u2/library/FMPro?-db=journalred.fp5&-format=/w2/JournalDetail.html&-lay=data&-Token.0=&-Token.3=COM-98-8265&-recid=33133&-Script=citation&-find
6. Jie Wu; Tianning Diao; Wei Sun; Yizhe Li. Expeditious Approach to Coumarins via Pechmann Reaction Catalyzed by Molecular Iodine or AgOTf. Synth. Comm., 2006, 36, 20, p. 2949-2956
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http://dx.doi.org/10.1080/00397910600773692
7. N. Takahashi, R. H. Dashwood, L. F. Bjeldanesa D. E. Williams, and G. S. Bailey. Mechanisms of Indole-3-carbinol (13C) anticarcinogenesis: Inhibition of aflatoxin b1-dna adduction and mutagenesis by 13C acid condensation products. Food and Chemical Toxicology, 1995, 33, 10, p. 851-857.
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http://dx.doi.org/10.1016/0278-6915(95)00054-6
8. Gyoonhee Han, Kye Jung Shin, Dong Chan Kim, Kyung Ho Yoo, Dong Jin Kim, and Sang Woo Park. A New Synthetic Route to 6,7-Dichloro-5,8-quinoxalinedione and Synthesis of Its Derivatives. Heterocycles, 1996, 43, 11, p. 2495-2502.
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https://www2.heterocycles.jp/u2/library/FMPro?-db=journalred.fp5&-format=/w2/JournalDetail.html&-lay=data&-Token.0=&-Token.3=COM-96-7586&-recid=33855&-Script=citation&-find