Synthesis of Novel Indolo‐Spirocyclic Compounds
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[1] M. Shiri,et al. Indoles in multicomponent processes (MCPs). , 2012, Chemical reviews.
[2] R. Rios. Enantioselective methodologies for the synthesis of spiro compounds. , 2012, Chemical Society reviews.
[3] M. Zupan,et al. Iodine-catalyzed transformation of molecules containing oxygen functional groups , 2011 .
[4] A. Kamal,et al. An efficient synthesis of bis(indolyl)methanes and evaluation of their antimicrobial activities , 2009, Journal of enzyme inhibition and medicinal chemistry.
[5] W. Dehaen,et al. A facile and general method for the synthesis of 6,12-diaryl-5,11-dihydroindolo[3,2-b]carbazoles. , 2009, Organic & biomolecular chemistry.
[6] Zheng Wang,et al. Spiro skeletons: a class of privileged structure for chiral ligand design. , 2009, Chemistry, an Asian journal.
[7] L. Jong,et al. Computer-aided rational drug design: a novel agent (SR13668) designed to mimic the unique anticancer mechanisms of dietary indole-3-carbinol to block Akt signaling. , 2007, Journal of medicinal chemistry.
[8] I. Mohammadpoor‐Baltork,et al. BiOClO4·xH2O and Bi(OTf)3 as Efficient and Environmentally Benign Catalysts for Synthesis of Bis(indolyl)methanes in Solution and Under Ultrasound Irradiation , 2006 .
[9] P. Seeberger,et al. Phosphoric acid-on-silica gel : A green catalyst for the synthesis of symmetrical bis(indolyl)alkanes , 2006 .
[10] Shiow-Ju Lee,et al. Synthesis and Cytotoxicity Studies of Cyclohepta[b]indoles, Benzo[6,7]Cyclohepta[1,2‐b]Indoles, Indeno[1,2‐b]Indoles, and Benzo[a]Carbazoles , 2006 .
[11] D. Shinde,et al. Zirconium(IV) Chloride - Catalysed Reaction of Indoles: An Expeditious Synthesis of Bis(indolyl)methanes , 2005 .
[12] M. Karthik,et al. Zeolite catalyzed electrophilic substitution reaction of indoles with aldehydes: synthesis of bis(indolyl)methanes , 2004 .
[13] I. Wagner-Döbler,et al. New indole alkaloids from the North Sea bacterium Vibrio parahaemolyticus Bio249. , 2003, Journal of natural products.
[14] C. Álvarez-Toledano,et al. Infrared-assisted eco-friendly selective synthesis of diindolylmethanes , 2003 .
[15] S. Klemenc. 4-Dimethylaminopyridine as a catalyst in heroin synthesis. , 2002, Forensic science international.
[16] L. Angenot,et al. Antiplasmodial activity of alkaloids from various strychnos species. , 2002, Journal of natural products.
[17] F. Sarkar,et al. Akt inactivation is a key event in indole-3-carbinol-induced apoptosis in PC-3 cells. , 2002, Clinical cancer research : an official journal of the American Association for Cancer Research.
[18] S. Antane,et al. Synthesis and potassium channel opening activity of substituted 10H-benzo[4,5]furo[3,2-b]indole-and 5,10-dihydro-indeno[1,2-b]indole-1-carboxylic acids. , 2001, Bioorganic & medicinal chemistry letters.
[19] T. Zacharewski,et al. Interaction of PAH-related compounds with the α and β isoforms of the estrogen receptor , 2001 .
[20] D. Alagille,et al. Synthesis and in vitro cytotoxic evaluation of N-substituted benzo[5,6]cycloheptal[b]indoles. , 2000, Chemical & pharmaceutical bulletin.
[21] Thomas Golob,et al. Antiestrogenic Activities of 3,8‐Dihydroxy‐6,11‐dihydrobenzo[a]carbazoles with Sulfur‐Containing Side Chains , 2000, Archiv der Pharmazie.
[22] M. Sannigrahi. Stereocontrolled synthesis of spirocyclics , 1999 .
[23] P. Renard,et al. Novel thiopyrano[3,2-b] and cycloalkeno[1,2-b]indole derivatives with high inhibitory properties in LTB4 production , 1999 .
[24] B. Joseph,et al. Synthesis and Antitumoral Evaluation of 12-Substituted 6,7-Dihydrobenzo[4,5]-cyclohept[1,2-b]indole Derivatives , 1998 .
[25] P. Wang,et al. Preparation, Characterization, and Synthetic Uses of Lanthanide(III) Catalysts Supported on Ion Exchange Resins , 1997 .
[26] P. Bhattacharyya,et al. Montmorillonite Clay-catalysed Synthesis of Bis(indol-3-yl)-methanes and 1,2-Bis(indol-3-yl)ethanes† , 1997 .
[27] A. Ivory,et al. Synthesis of indolo[3,2-b]carbazoles from 4,6-dimethoxyindole and aryl aldehydes 1 , 1995 .
[28] G. Gribble. Recent developments in indole ring synthesis—methodology and applications , 2010 .
[29] S. Aoki,et al. Marine natural products. XXXIV. Trisindoline, a new antibiotic indole trimer, produced by a bacterium of Vibrio sp. separated from the marine sponge Hyrtios altum. , 1994, Chemical & pharmaceutical bulletin.
[30] David W. Brown,et al. New antioxidants incorporating indole and indoline chromophores , 1991 .
[31] Y. Kanaoka,et al. The Plancher rearrangement of 2,3-disubstituted 3H-indoles , 1969 .
[32] W. Noland,et al. Cyclizative Condensations. I. 2-Methylindole with Acetone and Methyl Ethyl Ketone1 , 1961 .
[33] H. V. Dobeneck,et al. Über das Indolo‐(2.3‐b)‐carbazol und weitere Umsetzungsprodukte der Diindolyl‐(3.3′)‐methane (II. Mitteil. zur Chemie des Indols) , 1954 .
[34] O. Kruber. Zur Kenntnis der Chrysen‐Fraktion des Steinkohlenteerpechs , 1941 .