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299921.
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Development of a Diversity-Based Approach for the Discovery of Stereoselective Polymerization Catalysts: Identification of a Catalyst for the Synthesis of Syndiotactic Polypropylene This work was supported by the Cornell Center for Materials Research (CCMR), a Materials Research Science and Engineering Center of the National Science Foundation (DMR-9632275), and the Exxon Chemical Corporation. G.W.C. gratefully acknowledges an NSF Career Award (CHE-9875261), a Camille and Henry Dreyfus New Faculty Award, a Research Corporation Research Innovation Award, an Alfred P. Sloan Research Fellowship, an Arnold and Mabel Beckman Foundation Young Investigator Award, a Camille Dreyfus Teacher-Scholar Award, a 3M Untenured Faculty Grant, an IBM Partnership Award, and a Union Carbide Innovation Recognition Award. [electronic resource]
Publication details: Angewandte Chemie (International ed. in English) Oct 2000
In:
Angewandte Chemie (International ed. in English) vol. 39
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299922.
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Unprecedented Detection of Distinct Barriers Involving Formally Enantiotopic Substituents: Phenyl Rotation in Solid Diphenyl Sulfoxide Conformational Studies by Dynamic NMR. Part 82. For Part 80 see ref. 1a, for Part 81 see ref. 1b. We thank J. E. Anderson (University College, London, UK), S. E. Biali (Hebrew University, Jerusalem, Israel), R. K. Harris (University of Durham, UK), W. B. Jennings (University College, Cork, Ireland), A. Rassat (École Normale Superieure, Paris, France) for critical reading of the manuscript, and I.Co.C.E.A., CNR, Bologna for access to the 400-MHz and solid-state NMR spectroscopy facilities. Financial support was received from MURST (national project "Stereoselection in Organic Synthesis") and from the University of Bologna (Funds for selected research topics 1999-2001). [electronic resource] by
Publication details: Angewandte Chemie (International ed. in English) Jul 2001
In:
Angewandte Chemie (International ed. in English) vol. 40
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299923.
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299924.
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299925.
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299926.
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New 10-membered inorganic heterocyclic diphosphanes, PhN(PX)(2)[(-OC(6)H(2)((T)Bu)(2))(mu-S)(((t)Bu)(2)C(6)H(2)O-)] (x = cl, f). Synthesis and transition metal complexes (molybdenum(0), ruthenium(II), palladium(II), and platinum(II)) of heterocyclic diphosphanes. crystal and molecular structures of the chloro derivative, PhN(PCl)(2)[(-OC(6)H(2)((t)Bu)(2))(mu-S)(((t)Bu)(2)C(6)H(2)O-)], and of a molybdenum(0) complex of the fluoro derivative, [Mo(CO)(3)[eta(3)-PhN(PF)(2)[(-OC(6)H(2)((t)Bu)(2))(mu-S)(((t)Bu)(2)C(6)H(2)O-)]-kappa P,kappa P,kappa S]]. [electronic resource] by Producer: 20020104
In:
Inorganic chemistry vol. 40
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299927.
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299928.
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299929.
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The Spongistatins: Architecturally Complex Natural Products-Part Two: Synthesis of the C(29-51) Subunit, Fragment Assembly, and Final Elaboration to (+)-Spongistatin 2 Financial support was provided by the National Institutes of Health (National Cancer Institute) through Grant CA-70329, a NIH Postdoctoral Fellowship to C.S.B., a Japan Society for Promotion of Science Fellowship to N.M., and a Royal Society Fulbright Fellowship to V.A.D. We also thank the Daiichi Pharmaceutical Co., Ltd, and the Tanabe Seiyaku Co., Ltd for financial support. Finally we thank Dr George T. Furst, Dr. Patrick J. Carroll, and Dr. Rakesh Kohli of the University of Pennsylvania Spectroscopic Service Center for assistance in securing and interpreting high-field NMR spectra, X-ray crystal structures, and mass spectra, respectively. [electronic resource] by
Publication details: Angewandte Chemie (International ed. in English) Jan 2001
In:
Angewandte Chemie (International ed. in English) vol. 40
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299930.
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The Spongistatins: Architecturally Complex Natural Products-Part One: A Formal Synthesis of (+)-Spongistatin 1 by Construction of an Advanced ABCD Fragment Financial support was provided by the National Institutes of Health (National Cancer Institute) through Grant CA-70329, NIH Postdoctoral Fellowships to A.M.B. and W.H.M., a Japan Society for Promotion of Science Fellowship to N.M., and a Royal Society Fulbright Fellowship to V.A.D. We also thank the Daiichi Pharmaceutical Co., Ltd, and the Tanabe Seiyaku Co., Ltd for financial support. Finally we thank Dr. George T. Furst, Dr. Patrick J. Carroll, Dr. Rakesh Kohli, and Mr John Dykins of the University of Pennsylvania Spectroscopic Service Center for assistance in securing and interpreting high-field NMR spectra, X-ray crystal structures, and mass spectra. [electronic resource] by
- Smith III, Amos B
- Doughty, Victoria A
- Lin, Qiyan
- Zhuang, Linghang
- McBriar, Mark D
- Boldi, Armen M
- Moser, William H
- Murase, Noriaki
- Nakayama, Kiyoshi
- Sobukawa, Masao
Publication details: Angewandte Chemie (International ed. in English) Jan 2001
In:
Angewandte Chemie (International ed. in English) vol. 40
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299931.
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299932.
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Novel IBX-Mediated Processes for the Synthesis of Amino Sugars and Libraries Thereof We thank Dr. D. H. Huang, Dr. G. Siuzdak, and Dr. R. Chadha for NMR spectroscopic, mass spectrometric, and X-ray crystallographic assistance, respectively, and Prof. H. M. R. Hoffmann and Prof. A. Eschenmoser for helpful discussions. We also thank Dr. Maria-Rosa Rodriguez and Mr. Keith Wilcoxen of these laboratories for early intermediates leading to 9-12. This work was financially supported by the National Institutes of Health (USA), The Skaggs Institute for Chemical Biology, fellowships from the Ministerio de Educacion y Cultura, Spain (J.A.V.) and the National Science Foundation (P.S.B), and grants from Array Biopharma, Pfizer, GlaxoWellcome, Merck, Schering Plough, Hoffmann-LaRoche, Boehringer Ingelheim, DuPont, and Abbott Laboratories. [electronic resource]
Publication details: Angewandte Chemie (International ed. in English) Jul 2000
In:
Angewandte Chemie (International ed. in English) vol. 39
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299933.
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299934.
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