- Brian A. DeChristopher, Brian A. Loy, Matthew D. Marsden, Adam J. Schrier, Jerome A. Zack, & Paul A. Wender, “Designed, synthetically accessible bryostatin analogues potently induce activation of latent HIV reservoirs in vitro”, Nature Chemistry, 2012, 4, 705-710. Full Text.
- DeChristopher, Brian A., Fan, A.C., Felsher, D.W., Wender, Paul A., “”Picolog,” a Synthetically-Available Bryostatin Analog, Inhibits Growth of MYC-Induced Lymphoma in Vivo”; Oncotarget, 2012, 3(1), 58-66. Abstract, PDF, Full Text.
- Wender, P. A.; Baryza, J. L.; Brenner, S. E.; DeChristopher, B. A.; Loy, B. A.; Schrier, A. J.; Verma, V. A. "Function-Oriented Synthesis: Design, Synthesis and Evaluation of Potent Bryostatin Analogs that Modulate PKC Translocation Selectivity." Proc. Natl. Acad. Sci. USA. 2011, 108, 6721-6726. Abstract, PDF, Supporting Information.
- Wender, P. A.; Loy, B. A.; Schrier, A. J. "Translating Nature's Library: the Bryostatins and Function-Oriented Synthesis." Isr. J. Chem. 2011, 51, 453-472. Abstract, PDF.
- Wender, Paul A.; Longcore, Kate E.; “Apoptolidins E and F, New Glycosyated Macrolactones Isolated from Nocardopsis sp.” Organic Letters, 2009, 5474-5477. Abstract, PDF, Supporting Information.
- Wender, Paul A.; Miller, Benjamin L.; "Synthesis at the Molecular Frontier", Nature, 2009, 460, 197-201. Abstract, PDF.
- Lewis, Chad A.; Longcore, Kate E.; Miller, Scott J.; Wender, Paul A. “An Approach to the Site-Selective Diversification of Apoptolidin A with Peptide-Based Catalysts”, Journal of Natural Products, 2009, 72(10), 1864-1869. Abstract , PDF ,
Supporting Information.
- Mooberry, Susan; Hilinski, Michael; Clark, Erin; and Wender, Paul “Function-Oriented Synthesis: Biological Evaluation of Laulimalide Analogues Derived from a Last Step Cross Metathesis Diversification Strategy” Molecular Pharmaceutics; 2008; 5, 829-838.
Abstract, PDF.
- Wender, P.A.; DeChristopher, B.A.; Schrier, A.J. "Efficient Synthetic Access to a New Family of Highly Potent Bryostatin Analogues via a Prins-Drive Macrocyclization Strategy", J. Am. Chem. Soc.; 2008; 130(21); 6658-6659. Abstract, PDF, Supporting Information.
- Wender, P. A.; Verma, V. A. “The Design, Synthesis, and Evaluation of C7 Diversified Bryostatin Analogs Reveals a Hot Spot for PKC Affinity,” Org. Lett. 2008, 10, 3331. Abstract, Supporting Information.
- Wender, Paul A.; Verma, Vishal A.; Paxton, Thomas J.; Pillow, Thomas H. "Function Oriented Synthesis, Step Economy, and Drug Design", Accts. Chem. Res. 2008, 40-49.
Abstract,
PDF.
- Wender, P. A.; Longcore, K. E. "Isolation, Structure Determination, and Anti-Cancer Activity of Apoptolidin D" Org. Lett. 2007, 9, 691-694.
Abstract,
PDF,
Supporting Information.
- Wender, P. A.; Baryza, J. L.; Hilinski, M. K.; Horan, J. C.; Kan, C.; Verma, V. A. In Drug Discovery Research: New Frontiers in the Post-Genomic Era; Huang, Z.; Ed.; Wiley-VCH: 2007.
Abstract.
- Wender, P. A.; Horan, J. C.; Verma, Vishal A. "Total Synthesis and Initial Biological Evaluation of New B-Ring-Modified Bryostatin Analogues" Org. Lett. 2006, 8, 5299-5302.
Abstract,
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Supporting Information.
- Wender, P. A.; Horan, J. C. "Synthesis and PKC Binding of a New Class of A-Ring Diversifiable Bryostatin Analogues Utilizing a Double Asymmetric Hydrogenation and Cross-Coupling Strategy" Org. Lett. 2006, 8, 4581-4584.
Abstract,
PDF,
Supporting Information.
- Wender, P. A.; Hilinski, M. K.; Skaanderup, P. R.; Soldermann, N. G.; Mooberry, S. L. "Pharmacophore mapping in the laulimalide series: total synthesis of a vinylogue for a late-stage metathesis diversification strategy" Org. Lett. 2006, 8, 4105-4108.
Abstract,
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Supporting Information.
- Clark, E. A.; Hills, P. M.; Davidson, B. S.; Wender, P. A.; Mooberry, S. L. "Laulimalide and synthetic laulimalide analogues are synergisitic with paclitaxel and 2-methoxyestradiol" Molecluar Pharmaceutics 2006, 3, 457-467.
Abstract,
PDF.
- Wender, P. A.; Verma, V. A. "Design, Synthesis, and Biological Evaluation of a Potent, PKC Selective, B-Ring Analog of Bryostatin" Org. Lett. 2006, 8, 1893-1896.
Abstract,
PDF,
Supporting Information.
- Wender, P. A.; Hilinski, M. K.; Soldermann, N.; Mooberry, S. L. "Total Synthesis and Biological Evaluation of 11-Desmethyllaulimalide, a Highly Potent Simplified Laulimalide Analogue" Org. Lett. 2006, 8, 1507-1510.
Abstract,
PDF,
Supporting Information.
- Wender, P. A.; Jankowski, O. D.; Longcore, K.; Tabet, E. A.; Seto, H.; Tomikawa, T. "Correlation of F0F1-ATPase Inhibition and Antiproliferative Activity of Apoptolidin Analogues" Org. Lett. 2006, 8, 589-592.
Abstract,
PDF,
Supporting Information.
- Wender, P. A.; Sukopp, M.; Longcore, K. "Apoptolidins B and C: Isolation, Structure Determination, and Biological Activity" Org. Lett. 2005, 7, 3025-3028.
Abstract,
PDF,
Supporting Information.
- Wender, P. A.; Clarke, M. O.; Horan, J. C. "Role of the A-Ring of Bryostatin Analogues in PKC Binding: Synthesis and Initial Biological Evaluation of New A-Ring-Modified Bryologs" Org. Lett. 2005, 7, 1995-1998.
Abstract,
PDF,
Supporting Information.
- Wender, P. A.; Baryza, J. L. "Identification of a Tunable Site in Bryostatin Analogs: C20 Bryologs Through Late Stage Diversification" Org. Lett. 2005, 7, 1177-1180.
Abstract,
PDF,
Supporting Information.
- Wender, P. A.; Hilinski, M. K.; Mayweg, A. V. W. "Late-stage Intermolecular C-H Activation for Lead Diversification: A Highly Chemoselective Oxyfunctionalization of the C-9 Position of Potent Bryostatin Analogues" Org. Lett. 2005, 7, 79-82
Abstract,
PDF,
Supporting Information.
- Wender, P. A.; Baryza, J. L.; Brenner, S. E.; Clarke, M. O.; Craske, M. L.; Horan, J. C.; Meyer, T. "Function Oriented Synthesis: The Design, Synthesis, PKC Binding and Translocation Activity of a New Bryostatin Analog." Curr. Drug Disc. Tech., 2004; 1, 1-11.
Abstract.
- Mooberry, S. L.; Randall-Hlubek, D. A.; Leal, R. M.; Hegde, S. G.; Hubbard, R. D.; Zhang, L.; Wender, P. A. "Microtubule-Stabilizing Agents Based on Designed Laulimalide Analogues" Proc. Natl. Acad. Sci. U. S. A., 2004, 101, 8803-8808.
Abstract,
PDF
- Wender, P. A.; Hegde, S. G.; Hubbard, R. D.; Zhang, L.; Mooberry, S. L. "Synthesis and Biological Evaluation of (-)-Laulimalide Analogues" Org. Lett., 2003, 5, 5307-5309.
Abstract,
PDF,
Supporting Information
- Wender, P. A.; Jankowski, O. D.; Tabet, E. A.; Seto, H. "Facile Synthetic Access to and Biological Evaluation of the Macrocyclic Core of Apoptolidin " Org. Lett., 2003, 5, 2299-2302.
Abstract,
PDF,
Supporting Information
- Wender, P. A.; Baryza, J. L.; Brenner, S. E.; Clarke, M. O.; Gamber, G. G.; Horan, J. C.; Jessop, T. C.; Kan, C.; Pattabiraman, K.; Williams, T. J. "Inspirations from Nature. New Reactions, New Therapeutic Leads, and New Drug Delivery Systems" Pure Appl. Chem., 2003, 75, 143-156.
Abstract.
- Wender, P. A.; Mayweg, A. V. W.; VanDeusen, C. L. "A Concise, Selective Synthesis of the Polyketide Spacer Domain of a Potent Bryostatin Analogue" Org. Lett., 2003; 5, 277-279.
Abstract,
PDF,
Supporting Information
- Wender, P. A.; Jankowski, O. D.; Tabet, E. A.; Seto, H. "Toward a Structure-Activity Relationship for Apoptolidin: Selective Functionalization of the Hydroxyl Group Array" Org. Lett., 2003; 5, 487-490.
Abstract,
PDF,
Supporting Information
- Wender, P. A.; Baryza, J.; Bennett, C.; Bi, C.; Brenner, S. E.; Clarke, M.; Horan, J.; Kan, C.; Lacote, E.; Lippa, B.; Nell, P.; Turner, T. "The Practical Synthesis of a Novel and Highly Potent Analog of Bryostatin" J. Am. Chem. Soc. 2002, 124, 13648-13649.
Abstract,
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Supporting Information
- Wender, P. A.; Gulledge, A. V.; Jankowski, O. D.; Seto, H. "Isoapoptolidin: Structure and Activity of the Ring-Expanded Isomer of Apoptolidin" Organic Letters, 2002, 4, 3819-3822.
Abstract,
PDF,
Supporting Information
- Wender, P. A.; Lippa B. "Synthesis and Biological Evaluation of Bryostatin Analogues: the Role of the A-Ring" Tetrahedon Lett. 2000, 41, 1007-1011.
Abstract
- Wender, P. A.; Hinkle, K. W.; Koehler, M. F. T.; Lippa, B. "The Rational Design of Potential Chemotherapeutic Agents: Synthesis of Bryostatin Analogues" Med. Res. Rev. 1999, 19, 388-407.
Abstract,
PDF
- Wender, P. A.; Koehler, M. F. T.; Wright, D. L.; Irie, K. "Mapping Phorbol Ester Binding Domains of Protein Kinase C (PKC): the Design, Synthesis and Biological Activity of Novel Phorbol Ester Dimers" Synthesis 1999, 1401-1406.
- Wender, P. A.; Debrabander, J; Harran P. G.; Jimenez J. M.; Koehler M. F. T.; Lippa, B; Park, C. M.; Siedenbiedel, C.; Pettit, G. R. "The Design, Computer Modeling, Solution Structure, and Biological Evaluation of Synthetic Analogs of Bryostatin 1" Proc. Natl. Acad. Sci. U. S. A. 1998, 95, 6624-6629.
Abstract,
PDF
- Wender, P. A.; Debrabander, J.; Harran, P. G.; Jimenez, J. M.; Koehler, M. F. T.; Lippa, B.; Park, C. M.; Shiozaki, M."Synthesis of the First Members of A New Class of Biologically Active Bryostatin Analogues" J. Am. Chem. Soc. 1998, 120, 4534-4535.
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Supporting Information
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- Stang, Stacey L.; Lopez-Campistrous, Ana; Song, Xiaohua; Dower, Nancy A.; Blumberg, Peter M.; Wender, Paul A.; Stone, Jim “ A Pro-apoptotic Signaling Pathway involving RasGRP, Erk and Bim in B Cells” Experimental Hematology, 2009, 37, 122-134. Abstract.
- Shaha, S.P.; Tomic, J.; Shi, Y.; Pham, T.; Mero, P.; White, D.; He, L.; Baryza, J.L.; Wender, P.A.; Booth, J.W.; Spaner, D.E.; "Prolonging Microtubule Dysruption Enhances the Immunogenicity of Chronic Lymphocytic Leukemia Cells", Clinical & Experimental Immunolocy, 2009, 158, 186-198. Abstract, PDF.
- Tapan Kumar Khan; Thomas J Nelson; Vishal A Verma; Paul A Wender; Daniel L Alkon: “A Cellular Model of Alzheimer’s Disease Therapeutic Efficacy: PKC Activation Reverses A-beta induced biomarker Abnormality on Cultured Fibroblasts” Neurobiology of Disease 2009, 34(2), 332-339. Abstract, PDF.
- Statsuk, Alexander V.; Bai, Ruoli; Baryza, Jeremy L.; Verma, Vishal A.; Hamel, Ernest; Wender, Paul A.; Kozmin, Sergey A. "Actin is the primary cellular receptor of bistramide A" Nature Chemical Biology, 2005, 1, 383-388.
PDF,
Supporting Information
- Hammond, C.; Shi, Y. H.; Mena, J.; Tomic, J.; Cervi, D.; He, L. W.; Millar, A. E.; DeBenedette, M.; Schuh, A. C.; Baryza, J. L.; et. al. "Effect of Serum and Antioxidants on the Immunogenicity of Protein Kinase C-activated Chronic Lymphocytic Leukemia Cells" J. Immunotherapy 2005, 28, 28-39.
Abstract,
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- Stone, J. C.; Stang, S. L.; Zheng, Y.; Dower, N. A.; Brenner, S. E.; Baryza, J. L.; Wender, P. A. "Synthetic Bryostatin Analogues Activate the RasGRP1 Signaling Pathway" J. Med. Chem. 2004, 47, 6638-6644.
Abstract,
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- Baryza, J. L.; Brenner, S. E.; Craske, M. L.; Meyer, T.; Wender, P. A. "Simplified Analogs of Bryostatin with Anticancer Activity Display Greater Potency for Translocation of PKC delta-GFP" Chem. Bio. 2004, 11, 1261-1267.
- Chen, L; Wright, L. R.; Chen, C. H.; Oliver, S. F.; Wender, P. A.; Mochly-Rosen D. "Molecular Transporters for Peptides: Delivery of a Cardioprotective Epsilon PKC Agonist Peptide into Cells and Intact Ischemic Heart Using a Transport System, R-7"
Chemistry & Biology 2001, 8, 1123-1129.
Abstract,
PDF
- Shindo, M.; Irie, K.; Nakahara, A,; Ohigashi, H,; Konishi, H.; Kikkawa, U.; Fukuda, H.; Wender, P. A. "Toward the Identification of Selective Modulators of Protein Kinase C (PKC) Isozymes: Establishment of A Binding Assay for PKC Isozymes Using Synthetic C1 Peptide Receptors and Identification of the Critical Residues Involved in the Phorbol Ester Binding" Bioorg. Med. Chem. 2001, 9, 2073-2081.
Abstract
- Tanaka M, Irie K, Nakagawa Y, Nakamura Y, Ohigashi H, Wender, P. A."The C4 Hydroxyl Group of Phorbol Esters is not Necessary for Protein Kinase C Binding"
Bioorg. Med. Chem. Lett. 2001, 11, 719-722.
Abstract
- Nakagawa, Y.; Irie, K.; Ohigashi, H.; Hayashi, H.; Wender, P. A."Synthesis and PKC Isozyme Surrogate Binding of indothiolactam-V, A New Thioamide Analogue of Tumor Promoting indolactam-V" Bioorg. Med. Chem. Lett. 2000, 10, 2087-2090.
Abstract
- Wender, P. A.; Hinkle K. W. "Synthesis and Biological Evaluation of A New Class of Bryostatin Analogues: the Role of the C20 Substituent in Protein Kinase C Binding" Tetrahedon Lett. 2000, 41, 6725-6729.
Abstract
- Fukuda, H,; Irie, K,; Nakahara, A.; Ohigashi, H.; Wender, P. A. "Solid-Phase Synthesis, Mass Spectrometric Analysis of the Zinc-Folding, and Phorbol Ester-Binding Studies of the 116-Mer Peptide Containing the Tandem Cysteine-Rich C1 Domains of Protein Kinase C Gamma" Bioorg. Med. Chem. 1999, 7, 1213-1221.
- Wender, P. A.; Kirschberg, T. A.; Williams, P. D.; Bastiaans, H. M. M.; Irie, K. "A New Class of Simplified Phorbol Ester Analogues: Synthesis and Binding To PKC and Eta PKC-C1b (Eta PKC-Cpd2)" Org. Lett. 1999, 1, 1009-1012.
Abstract,
PDF,
Supporting Information,
- Wender, P. A.; Koehler, M. F. T.; Wright, D. L.; Irie, K. "Mapping Phorbol Ester Binding Domains of Protein Kinase C (PKC): the Design, Synthesis and Biological Activity of Novel Phorbol Ester Dimers" Synthesis 1999, 1401-1406.
- Irie, K.; Oie, K.; Nakahara, A.; Yanai, Y.; Ohigashi, H.; Fukuda, H.; Wender, P. A. "Synthesis and Phorbol Ester Binding of the Zinc-finger Like Sequences of All Protein Kinase C Isozymes, In Peptide Science 1998, M. Kondo, Ed.: Protein Research Foundation, Osaka , 65-68, 1999.
- Wender, P. A.; Lippa, B.; Park, C. M.; Irie, K.; Nakahara, A.; Ohigashi, H. "Selective Binding of Bryostatin Analogues To the Cysteine Rich Domains of Protein Kinase C Isozymes" Bioorg. Med. Chem. Lett. 1999, 9, 1687-1690.
- Fukuda, H.; Irie, K.; Nakahara, A.; Oie, K.; Ohigashi, H.; Wender, P. A. "Synthesis and Binding Studies of the 116-Mer Peptide Containing the Double Cysteine-Rich Motifs of Protein Kinase C Gamma" Tetrahedon Lett. 1998, 39, 7943-7946.
- Wender, P. A.; Martincantalejo, Y.; Carpenter, A. J., Chiu, A.; Debrabander, J.; Harran, P. G.; Jimenez, J. M.; Koehler, M. F. T; Lippa, B."The Chemistry-Medicine Continuum: Synthetic, Computer, Spectroscopic and Biological Studies on New Chemotherapeutic Leads" Pure Appl. Chem. 1998, 70, 539-546.
- Irie, K.; Oie, K.; Nakahara, A.; Yanai, Y.; Ohigashi, H.; Wender, P. A.; Fukuda, H.; Konishi, H.; Kikkawa, U."Molecular Basis for Protein Kinase C Isozyme-Selective Binding: the Synthesis, Folding, and Phorbol Ester Binding of the Cysteine-Rich Domains of All Protein Kinase C Isozymes" J. Am. Chem. Soc. 1998, 120, 9159-9167.
Abstract,
PDF,
Supporting Information,
- Wender, P. A.; Debrabander, J; Harran P. G.; Jimenez J. M.; Koehler M. F. T.; Lippa, B; Park, C. M.; Siedenbiedel, C.; Pettit, G. R. "The Design, Computer Modeling, Solution Structure, and Biological Evaluation of Synthetic Analogs of Bryostatin 1" Proc. Natl. Acad. Sci. U. S. A. 1998, 95, 6624-6629.
Abstract,
PDF,
- Irie, K.;Yanai, Y.; Ohigashi, H.; Wender, P. A. "Synthesis and Characterization of Model Peptides Incorporating the Phorbol Ester-binding Domain of Protein Kinase C," Peptide Chemistry 1996: C. Kitada (Ed.), Protein Research Foundation, Osaka, 209, 1997.
- Yanai, Y.; Irie, K.; Ohigashi, H.; Wender, P. A. "Synthesis and Characterization of the First Cysteine-Rich Domain of Novel Protein Kinase C" Bioorg. Med. Chem. Lett. 1997, 7, 117-122.
- Irie, K.; Yanai, Y.; Oie, K.; Ohigashi, H.; Wender, P. A. "Protein Kinase C Regulatory Domain Surrogate Peptides: Effects of Metal Ions on Folding, Phorbol Ester-Binding, and Selectivity" Bioorg. Med. Chem. Lett. 1997, 7, 965-970.
- Irie, K.; Yanaim, Y.; Oie, K.; Ishizawa, J.; Nakagawa, Y.; Ohigashi, H.; Wender, P. A.; Kikkawa, U. "Comparison of Chemical Characteristics of the First and the Second Cysteine-Rich Domains of Protein Kinase C Gamma" Bioorg. Med. Chem. 1997, 5, 1725-1737.
- Irie, K.; Isaka, T.; Iwata, Y.; Yanai, Y.; Nakamura, Y.; Koizumi, F.; Ohigashi, H.; Wender, P. A.; Satomi, Y.; Nishino, H. "Synthesis and Biological Activities of New Conformationally Restricted Analogues of (-)-Indolactam-V: Elucidation of the Biologically Active Conformation of the Tumor-Promoting Teleocidins" J. Am. Chem. Soc. 1996, 118, 10733-10743.
Abstract,
PDF,
Supporting Information
- Irie, K.; Yanai, Y.; Ohigashi, H.; Wender, P. A.; Miller, B. L."Synthesis and Characterization of the Second Cysteine-Rich Region of Mouse Skin PKC Eta" Bioorg. Med. Chem. Lett. 1996, 6, 353-356.
- Irie, K.; Ishii, T.; Ohigashi, H.; Wender, P. A.; Miller B. L.; Takeda, N."Synthesis and Characterization of New Photolabile Phorbol Esters for Affinity Labeling of Protein Kinase C" J. Org. Chem. 1996, 61, 2164-2173.
Abstract,
PDF,
Supporting Information
- Wender, P. A.; Irie, K.; Miller, B. L."Identification, Activity, and Structural Studies of Peptides incorporating the Phorbol Ester-Binding Domain of Protein-Kinase-C" Proc. Natl. Acad. Sci. U. S. A. 1995, 92, 239-243.
Abstract,
PDF
- Irie, K.; Koizumi, F.; Iwata, Y.; Ishii, T.; Yanai, Y.; Nakamura, Y.; Ohigashi, H.; Wender, P. A. "Synthesis and Biological-Activities of New Conformationally Fixed Analogs of (-)-indolactam-V, the Core Structure of Tumor-Promoting Teleocidins" Bioorg. Med. Chem. Lett. 1995, 5, 453-458.
- Wender, P. A.; Irie, K.; Miller, B. L. "Synthesis and Binding of Photoaffinity Ligand Candidates for Protein-Kinase-C" J. Org. Chem. 1993, 58, 4179-4181.
- Wender, P. A.; Cribbs, C. M. "Structural Design in Anti-tumor Compounds." In Molecular Mechanisms and Their Clinical Applications in Malignancies; Bergsagel, Daniel E. and Mak, Tak W., Eds.; Academic ; San Diego, CA, 215, 1991.
- Wender, P. A.; Cribbs, C. M. "Computer Assisted Molecular Design Related to the Protein Kinase C Receptor," In Advances in Medicinal Chemistry; Maryanoff, C.A., Maryanoff, B.E., Eds.; JAI; Greenwich, CT; 1, 1-53, 1992.
- Wender, P. A. "Chemsitry, Computers, and Carcinogenesis" Pure Appl. Chem., 1989, 61, 469.
- Wender, P. A.; Koehler, K. F.; Sharkey, N. A.; Dellaquila, M. L.; Blumberg, P. M. "Analysis of the Phorbol Ester Pharmacophore on Protein-Kinase-C As a Guide To the Rational Design of New Classes of Analogs" Proc. Natl. Acad. Sci. U. S. A. 1986, 83, 4214-4218.
- Wender, P. A.; Koehler, K.; Wilhelm, R.; Williams, P.; Keenan, R.; Lee, H. Y. "Tumor Promotion: Pharmacological and Synthetic Studies," in New Synthetic Methodology and Functionally Interesting Compounds, Z-I. Yoshida, Ed.; pp. 163-184, Elsevier Publishing Co., Amsterdam 1986.
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- Wender, P. A., “The Future of Chemistry – What Lies Ahead – Look Through a Molecular Lens”, Nature, 2011, 469, 23-25. Article.
- Wender, P. A.; Jeon, R. "Photoinduced Cleavage of DNA by Bromofluoroacetophenone-pyrrolecarboxamide Conjugates" Bioorg. Med. Chem. Lett. 2003, 13, 1763-1766.
- Jeon, R; Wender, P. A. "Photocleavage of DNA By 4'-Bromoacetophenone Analogs". Arch. Pharm. Res. 2001, 24, 39-43.
- Irie, K.; Nakahara, A.; Ikawa, Y.; Tanaka, M.; Nakagawa, Y.; Nakamura, Y.; Ohigashi, H.; Wender, P. A."Synthesis and Tumor-Promoting Activities of 12-Epi-Phorbol-12, 13-Dibutyrate" Biosci. Biotech. Biochem. 2000, 64, 2429-2436.
- Jeon, R.; Wender, P. A. "Design and Synthesis of New DNA Photocleavers, 4'-Bromoacetophenone-Pyrrolecarboxamide Hybrid Compounds." Arch. Pharm. Res. 2000, 23, 585-588.
- Wender, P. A.; Jeon, R. "Bromoacetophenone-Based Photonucleases: Photoinduced Cleavage of DNA By 4'-Bromoacetophenone-Pyrrolecarboxamide Conjugates" Org. Lett. 1999, 1, 2117-2120.
- Irie, K; Nakahara, A.; Ohigashi, H.; Fukuda, H.; Wender, P. A.; Konishi, H.; Kikkawa, U. "Synthesis and Phorbol Ester-Binding Studies of the individual Cysteine-Rich Motifs of Protein Kinase D" Bioorg. Med. Chem. Lett. 1999, 9, 2487-2490.
- Wender, P. A.; Debrabander, J.; Harran, P. G.; Hinkle, K.W.; Lippa, B.; Pettit, G. R. "Synthesis and Biological Evaluation of Fully Synthetic Bryostatin Analogues" Tetrahedon Lett. 1998, 39, 8625-8628.
- Wender, P. A.; Delong, M. A.; Wireko, F. C. "Novel Oxidative Rearrangement Product of the First Trans,cis,cis,cis-[5.5.5.5]Fenestrane Derivative" Acta Crystallographica C-Crystal Structure Comm.1997, 53, 954-956.
- Wender, P. A.; Lee, D. S., Lal, T. K., Horwitz, S. B.; Rao, S."Synthesis of Novel Taxol Analogs and Evaluation of their Biological Activities" Bioorg. Med. Chem. Lett. 1997, 7, 1941-1944.
- Yang, J. W.; Wender, P. A. "Synthesis of 1-(2-Naphthoyl) Benzotriazoles As Photoactivated DNA Cleaving Agents" Arch. Pharm. Res. 1997, 20, 197-199.
- Touami, S. M., Poon, C. C., Wender, P. A. "Sequence Specific DNA Cleavage By Conjugates of Benzotriazoles and Minor Groove Binders" J. Am. Chem. Soc. 1997, 119, 7611-7612.
- Wender, P. A. "Frontiers in Organic Synthesis: Introduction" Chem. Rev. 1996, 96, 1-2.
- Wender, P. A.; Touami, S. M.; Alayrac, C; Philipp, U. C. "Triazole Photonucleases: A New Family of Light Activatable DNA Cleaving Agents" J. Am. Chem. Soc. 1996, 118, 6522-6523.
- Wender, P. A.; Glass, T. E.; Krauss, N. E.; Muhlebach, M.; Peschke, B.; Rawlins, D. B. "The Pinene Path To Taxanes .4. Approaches to Taxol and Taxol Analogs Through Elaboration of Aromatic C-Ring Precursors" J. Org. Chem. 1996, 61, 7662-7663.
- Wender, P. A.; Wessjohann, L. A.; Peschke, B.; Rawlins, D. B. "The Pinene Path to Taxol: Readily Accessible A-Ring Building-Blocks Based on Novel Alkyllithium and Alkenyllithium Reagents with Internal Carbonyl Groups" Tetrahedon Lett. 1995, 36, 7181-7184.
- Wender, P. A.; Floreancig, P. E.; Glass, T. E.; Natchus, M. G.; Shuker, A. J.; Sutton, J. C. "Toward the Synthesis of Taxol and its Analogs: incorporation of Nonaromatic C-Rings in the Pinene Pathway" Tetrahedon Lett. 1995, 36, 4939-4942.
- Wender, P. A.; Beckham, S.; Mohler, D. L. "The Intramolecular Addition of Silylated Alkynes to Aldehydes: Methodology for the Construction of Cyclic Enediynes and Its Application to Dynemicin Analogs" Tetrahedon Lett. 1995, 36, 209-212.
- Wender, P. A.; Glass T. E. "The Pinene Approach to Taxanes .2. Development of A Versatile C9, C10 Linker" Synlett 1995, 516-518.
- Wender, P. A.; Tebbe, M. J. "The Synthesis and Chemistry of a Simplified, Functional Analog of Neocarzinostatin Chromophore: Identification of An Intramolecular 1,5-Hydrogen Atom-Transfer Relevant to the Mechanism and Cleavage Selectivity of Diyl-Based DNA-Cleaving Agents" Tetrahedron 1994, 50, 1419-1434.
- Wender, P. A.; Zercher, C. K.; Beckham, S.; Haubold, E.M.>"A Photochemically Triggered DNA-Cleaving Agent: Synthesis, Mechanistic and DNA Cleavage Studies on a New Analog of the Antitumor Antibiotic Dynemicin" J. Org. Chem. 1993, 58, 5867-5869.
- Wender, P. A.; Rawlins D. B."Toward the Synthesis of the Taxol C,D Ring-System: Photolysis of Alpha-Methoxy Ketones" Tetrahedron 1992, 48, 7033-7048.
- Wender, P. A.; Mascarenas, J. L."Preparation and Cycloadditions of a 4-Methoxy-3-Oxidopyrylium Ylide: A Reagent for the Synthesis of Highly Substituted 7-Membered Rings and Tetrahydrofurans" Tetrahedon Lett. 1992, 33, 2115-2118.
- Wender, P. A.; Kelly R. C.; Beckham, S.; Miller, B. L. "Studies on DNA-Cleaving Agents: Computer Modeling Analysis of the Mechanism of Activation and Cleavage of Dynemicin Oligonucleotide Complexes" Proc. Natl. Acad. Sci. U. S. A. 1991, 88, 8835-8839.
- Wender, P. A.; Mascarenas J. L. "Studies on Tumor Promoters .11. A New [5+2] Cycloaddition Method and Its Application To the Synthesis of BC. Ring Precursors of Phoboids"J. Org. Chem. 1991, 56, 6267-6269.
- Wender, P. A.; Tebbe, M. J. "Studies on DNA Cleaving Agents: Synthesis and Chemically-Induced Cycloaromatization of a Monocyclic Neocarzinostatin Chromophore Analog"
Tetrahedon Lett. 1991, 32, 4863-4866.
- Wender, P. A.; Zercher, C.K. "Studies on DNA-Cleaving Agents: Synthesis of A Functional Dynemicin Analog" J. Am. Chem. Soc. 1991, 113, 2311-2313.
- Wender, P. A.; Grissom J. W.; Hoffmann, U.; Mah, R. "Heteroatom Substituted Chromium Allyls: Synthetic Studies on Neocarzinostatin Chromophore Analogs" Tetrahedon Lett. 1990, 31, 6605-6608.
- Wender, P. A.; Manly, C. J. "Discovery of A New Fragmentation Reaction" J. Am. Chem. Soc. 1990, 112, 8579-8581.
- Wender, P. A.; Mcdonald, F. E. "Studies on Tumor Promoters .10. Synthesis of the ABC Ring-System of the Tiglianes and Daphnanes By A Zirconium-Mediated Intramolecular Enyne Carbocyclization" Tetrahedon Lett. 1990, 31, 3691-3694.
- Wender, P. A.; Mckinney, J. A.; Mukai, C. "General Methodology for the Synthesis of Neocarzinostatin Chromophore Analogs: Intramolecular Chromium-Mediated Closures for Strained-Ring Synthesis"J. Am. Chem. Soc. 1990, 112, 5369-5370.
- Wender, P. A.; Lee, H. Y.; Wilhelm, R. S.; Williams P. D."Studies on Tumor Promoters .7. the Synthesis of A Potentially General Precursor of the Tiglianes, Daphnanes, and Ingenanes" J. Am. Chem. Soc. 1989, 111, 8954-8957.
- Wender, P. A.; Cribbs, C. M.; Koehler, M. K. F., Sharkey, N. A.; Herald, C. L.; Kamano, Y.; Pettit, G. R.; Blumberg, P. M. "Modeling of the Bryostatins to the Phorbol Ester Pharmacophore on Protein Kinase-C" Proc. Natl. Acad. Sci. U. S. A. 1988, 85, 7197-7201.
- Wender, P. A.; Brighty, K."Studies on Tumor Promoters .5. Complementary 1,4-Stereocontrol in Phorboid Cycloheptene Synthesis Via the Divinylcyclopropane Rearrangement" Tetrahedon Lett. 1988, 29, 6741-6744.
- Wender, P. A.; Cooper, C. B. "Indole Synthesis Based on Triazole Photochemistry: Total Synthesis of 7 Methoxymitosene" Tetrahedon Lett. 1987, 28, 6125-6128.
- Wender, P. A.; Keenan, R. M., Lee, H. Y. "Studies on Tumor Promoters: the 1st Synthesis of the Phorbol Skeleton" J. Am. Chem. Soc. 1987, 109, 4390-4392.
- Wender, P. A.; Correia, C. R. D."Intramolecular Photoinduced Diene-Diene Cycloadditions: A Selective Method for the Synthesis of Complex 8-Membered Rings and Polyquinanes" J. Am. Chem. Soc. 1987, 109, 2523-2525.
- Wender, P. A.; Cooper, C. B."The Photochemistry of 1-Alkenylbenzotriazoles: Methodology for the Synthesis of Indoles" Tetrahedron 1986, 42, 2985-2991.
- Wender, P. A.; Ternansky, R. J.; Sieburth, S.M."Macroexpansion Methodology .5. An Enolate-Accelerated Cope Rearrangement" Tetrahedon Lett. 1985, 26, 4319-4322.
- Wender, P. A.; White, A. W. "Methodology for the Facile and Regio-Controlled Synthesis of Indoles" Tetrahedron 1983, 39, 3767-3776.
- Wender, P. A.; Holt, D. A.; Sieburth, S. M. "Practical Method for Alpha-Alkenyl Ketone Synthesis Based on A Facile Reductive Rearrangement of Alkynyl Halohydrins" J. Am. Chem. Soc. 1983, 105, 3348-3350.
- Wender, P. A.; Sieburth, S. M. "Macroexpansion Methodology: An Efficient 8 Unit Ring Expansion" Tetrahedon Lett. 1981, 22, 2471-2474.
- Wender, P. A.; Erhardt, J. M.; Letendre, L.J."Reaction of Allylically Substituted Enolates With Organometallic Reagents: A Convenient Source of Enolonium Ion Equivalents" J. Am. Chem. Soc. 1981, 103, 2114-2116.
- Wender, P. A.; White, A. W. "Methodology for Indole Synthesis" Tetrahedon Lett. 1981, 22, 1475-1478.
- Wender, P. A.; Sieburth, S. M.; Petraitis, J. J.; Singh, S. K."Macroexpansion Methodology: Medium Ring Synthesis Based on An 8 Unit Ring Expansion Process" Tetrahedron 1981, 37, 3967-3975.
- Wender, P. A.; Hillemann C. L., Szymonifka, M. J. "An Approach To the Tiglianes, Daphnanes, and Ingenanes Via the Divinylcyclopropane Rearrangement" Tetrahedon Lett. 1980, 21, 2205-2208.
- Wender, P. A.; Schaus, J. M.; Torney D.C."General-Method for cis-Hydroisoquinoline Synthesis" Tetrahedon Lett. 1979 2485-2488.
- Wender, P. A.; Eissenstat, M. A."Regiospecific Generation of Lithio-Enamines From Alpha,Beta-Unsaturated Imines: Alternative Method for Reduction-Alkylation of Enones" J. Am. Chem. Soc. 1978, 100, 292-294.
- Wender, P. A.; Schaus, J. M. "Imine Prototropy: Synthetic Consequences in Generation of Metalloenamines" J. Org. Chem. 1978, 43, 782-784.
- Wender, P. A.; Lechleiter, J. C. "Methods for Preparation of 1,5-Dienes: Metathetical Route To Medium-Sized Carbocycles" J. Am. Chem. Soc. 1977, 99, 267-268.
- Wender, P. A.; Eck, S. L. "Organobiscuprates: Single-Step Spiroannelation Method" Tetrahedon Lett. 1977, 1245-1248.
- Wender, P. A.; Filosa, M. P. "Facile Route to Divinylcyclopropanes: Efficient Method for Annelative Formation of Functionalized Cycloheptanes" J. Org. Chem. 1976, 41, 3490-3491.
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