Coleman, Robert S. - Department of Chemistry, Ohio State University

• Temlmhn Lettm. Vol. 34. No. 43, pi 6867-6870.1993 00404039193 $6.00 + DO Printedin GreatBritain Pcrg-PressIAd
• J. Am. Chem. SOC.1992, 114,9229-9230 9229 endolipasomalfunctional head groupsto exolipasomalloci,whereas
• Total synthesis of strobilurin B using a hetero-bis-metallated pentadiene Robert S. Coleman* and Xiaoling Lu
• J. Org. Chem. 1992,57,6813-5815 Synthesis of the Aziridino[1,243 Ipyrrolidine Substructure of the Antitumor Agents
• The Perfect Margarita Rob Coleman
• Role of the Azinomycin Naphthoate and Central Amide in Sequence-Dependent
• Studies on the Mechanism of Action of Azinomycin B: Definition of Regioselectivity and Sequence Selectivity of
• Synthesis of Functional "Top-Half" Partial Structures of Azinomycin A and B
• A Direct and Efficient Total Synthesis of the Tubulin-Binding Agents Ceratamine
• Synthesis of a Novel Coumarin C-Riboside as a Photophysical Probe of
• Power-Law Solvation Dynamics in DNA over Six Decades in Time Daniele Andreatta, J. Louis Perez Lustres, Sergey A. Kovalenko, Nikolaus P. Ernsting,*,
• Ultrafast Dynamics in DNA: "Fraying" at the End of the Helix Daniele Andreatta, Sobhan Sen, J. Luis Perez Lustres, Sergey A. Kovalenko,
• Stereocontrolled Synthesis of the Diene and Triene Macrolactones of Oximidines
• Asymmetric Total Synthesis of Dibenzocyclooctadiene Lignan Natural Products
• Total Synthesis of the Eupomatilones Soumya Mitra, Srinivas Reddy Gurrala, and Robert S. Coleman*
• 2240 J.Org. Chem. 1984, 49, 2240-2245 The enantiomeric excesswas >97% as measured by 'H NMR
• 1350 J. Am. Chem. SOC. multiple additions of MDA units to the initial MDA-base adduct.ls
• J. Org. Chem. 1987,52,1521-1530 1521 aqueous NaOH (0.35mL), and finally water (0.35 mL). The
• J. Org. Chem. 1988,53,695-698 695 on standing. Also obtained was (2)-enelactam4a (11.4 mg, 3%)
• J. Am. Chem. SOC. geometry and a metal-metal bond, d(Ir-Ir) = 2.7861 ( 6 ) A.
• Chem.-Biol Interactions, 73 (1990) 29-52 Elsevier Scientific Publishers Ireland Ltd.
• J. Am. Chem. Soc. 1990, 112, 3253-3255 3253 The conversion of 8 to 9 was effected with the Tebbe. reagentg
• J. Am. Chem. SOC.1990,112,4623-4632 4623 Synthesis and Evaluation of Aborted and Extended CC-1065
• J. Org. Chem. 1993,58,386392 386 Acylketene [4 +21 Cycloadditions: Divergent de Novo Synthesis of
• J. Am. Chem. SOC.1994,116,8795-8796 a795 AtropdiastereoselectiveTotal Synthesis of Phleichrome
• 11636 J. Am. Chem. SOC.1994,116, 11636-11642 Synthesis and Postsynthetic Modification of
• J. Am. Chem. SOC.1995,117, 10889-10904 10889 Synthesis of Helically Chiral Molecules: Stereoselective
• Stereocontrolled Synthesis of the Fully Elaborated Aziridine Core of the Azinomycins
• www.elsevier.nl/locate/ica Inorganica Chimica Acta 297 (2000) 5663
• Entropy Contributions to DNA-Promoted and DNA-Retarded Chemistry Revealed by Reactions of
• Mitomycin Synthetic Studies: Stereocontrolled and Convergent Synthesis of a Fully Elaborated Aziridinomitosane
• Synthesis of L-Daunosamine and L-Ristosamine Glycosides via Photoinduced Aziridination. Conversion to Thioglycosides for Use in
• VOLUME 88, NUMBER 15 P H Y S I C A L R E V I E W L E T T E R S 15 APRIL 2002 Complex Local Dynamics in DNA on the Picosecond and Nanosecond Time Scales
• PAPER www.rsc.org/obc | Organic & Biomolecular Chemistry Synthesis and DNA-binding affinity studies of glycosylated intercalators
• Synthesis of the Azabicyclic Core of the Azinomycins: Introduction of Differentiated
• Divergent and Stereocontrolled Synthesis of the Enamide Side Chains
• Measurement of Local DNA Reorganization on the Picosecond and Nanosecond Time Scales
• 3850 J. Am. Chem. Sot. 1991, 113, 3850-3866 19 (0.141 g, 94%) as a syrup: IR (neat) umax2960, 2873, 1716, 1450,
• * TetrahedronLetten.Vol.35 No.26.pi 3033-3034.1991 PrintedinGreatBritain
• Effect of lesions on the dynamics of DNA on the picosecond and nanosecond timescales using a
• TETRAHEDRON Tetrahedron Letters 44 (2003) 12151219Pergamon
• SHORT PAPER 1399 Synthesis 1999, No. SI, 13991400 ISSN 0039-7881 Thieme Stuttgart New York
• Dependence of DNA Sequence Selectivity and Cell Cytotoxicity on
• COMMUNICATIONS 1736 WILEY-VCH Verlag GmbH, D-69451 Weinheim, 2001 1433-7851/01/4009-1736 $ 17.50+.50/0 Angew. Chem. Int. Ed. 2001, 40, No. 9
• Molecular Modeling of the Antitumor Agents Azinomycins A and B: Force-Field Parametrization and DNA Cross-Linking-Based
• J.Org. Chem. 1985,50,5377-5379 5377 Table I. Reactions of Formaldehyde in Aqueous HX
• and `HNMR comparison with authentic material. J. Am. Chem. SOC.1988, 110, 4196-4801
• Temhedmnhen, VoL34, No.14.pp.+2225-m, 1993 -9/93 sao+ .oo RilWdillQWtBtiUill PagmcalReuLtd
• Tetrahedron Letters,Vol.28,No.lO,pp 1027-1030,1987 0040-4039/87 $3.00 + .Oo Printed in Great Britain Perqamon Journals Ltd.
• Total Synthesis of 2-O-Methylmyxalamide D and (6E)-2-O-Methylmyxalamide D
• Termhedmn Letters, Vol. 35. No. 45, pp. 8341-8344, 1994 Elsevin Science Led
• 3732 J.Org. Chem. 1992,57,3732-3735 at 60 OC for 6 h. The cooled reaction mixture was diluted with
• 5436 J.Org. Chem. 1986,51, 5436-5439 between ethyl acetate (30mL) and water (25 mL). The organic
• J. Org. Chem. 1990, 55, 2771-2776 Efficient Preparation of Intermediates Corresponding to C22427 and
• Coumarin base-pair replacement as a fluorescent probe of ultrafast DNA dynamics
• 1997 Oxford University Press 47714777Nucleic Acids Research, 1997, Vol. 25, No. 23 Covalent cross-linking of duplex DNA using
• J. Org. Chem. 1991,56,1357-1359 1357 The preparation of the tripeptide portion of jasplaki-
• 4462 J. Org. Chem. 1993,58, 4452-4461 Stereoselective Bromination of Dehydroamino Acids with
• Total Synthesis of Lucilactaene, A Cell Cycle Inhibitor Active in p53-Inactive Robert S. Coleman,* Matthew C. Walczak, and Erica L. Campbell
• Chemistry & Biology 13, 485492, May 2006 2006 Elsevier Ltd All rights reserved DOI 10.1016/j.chembiol.2006.02.015 Cellular Effects Induced by the
• 3ioosgonic & Medkhl Chmtimy Laners, Vol. 4. No. 15, pp. 1869-1872, 1994 copy+ Q 1994 Elsevier sci@nce Ltd
• Synthesis of the Spirocyclic Cyclohexadienone Ring System of the
• TeinhedmnLetten.Vol.31.No.26,pp36773680.1990 PrintedinGreatBritain
• 6252 J. Org. Chem. 1996,60, 6252-6253 Template-DirectedCross-Linkingof
• TetrahedronLcttcrs. Vol. 33, No. 13, pp. 1697-1700.1992 Printed in Great Britain
• Sodium-Ion Binding to DNA: Detection by Ultrafast Time-Resolved Stokes-Shift Spectroscopy
• J. Am. Chem. SOC.1987, 109, 2717-2727 2717 (from acetone); IR (Nujol) 3320, 2600, 1686, 1640, 1578, 1535, 1296,
• Total Synthesis of Gymnoconjugatins A and B Robert S. Coleman* and Matthew C. Walczak
• A Convergent Approach to the Mitomycin Ring System
• Tandem Stille/Suzuki-Miyaura Coupling of a Hetero-Bis-metalated Diene. Rapid,
• Role of Monovalent Counterions in the Ultrafast Dynamics of DNA Sobhan Sen, Latha A. Gearheart, Evan Rivers, Hai Liu, Robert S. Coleman,
• ACCOUNTS 1031 Issues of Orthogonality and Stability: Synthesis of the Densely Functionalized Heterocyclic
• J.Org. Chenz. 1984,49,4405-4409 Thermal Cycloaddition of Dimethyl 1,2,4,5-Tetrazine-3,6-dicarboxylatewith
• DNA Cross-Linking by Azinomycin B: Monte Carlo Simulations in the Evaluation of Sequence Selectivity
• Effect of Protein Binding on Ultrafast DNA Dynamics: Characterization of a DNA:APE1 Complex
• Total Synthesis of Eupomatilones 4 and 6: Structurally Rearranged and
• Synthesis of Naturally Occurring Antitumor Agents: Stereocontrolled Synthesis of the Azabicyclic Ring System of the Azinomycins
• Asymmetric Synthesis of the Dibenzocyclooctadiene Lignans
• 3250 J. Org. Chem. 1986,51, 3250-3252 stereoelectronically acceptable, but models show that it
• Molecular Modeling of DNA Cross-linking Analogues Based on the Azinomycin Scaffold Stefano Alcaro,*, Francesco Ortuso, and Robert S. Coleman