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299901.
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299902.
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299903.
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Synthesis of the FGHI Ring System of Azaspiracid We thank Dr. D. H. Huang and Dr. G. Siuzdak for NMR spectroscopic and mass spectrometric assistance, respectively. Financial support for this work was provided by The Skaggs Institute for Chemical Biology, the National Institutes of Health (USA), a predoctoral fellowship from Bristol-Myers Squibb (F.B.), postdoctoral fellowships from the Academy of Finland, the Ella and Georg Ehrnrooth Foundation, and the Tauno Tönning Foundation (all to P.M.P.), ArrayBiopharma (N.Z.), and Bayer AG (N.D.), and grants from Abbott, Amgen, ArrayBiopharma, Boehringer-Ingelheim, Glaxo, Hoffmann-LaRoche, DuPont, Merck, Novartis, Pfizer, and Schering Plough. [electronic resource] by
Publication details: Angewandte Chemie (International ed. in English) May 2001
In:
Angewandte Chemie (International ed. in English) vol. 40
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299904.
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299905.
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299906.
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Synthesis of the FGHI Ring System of Azaspiracid We thank Dr. D. H. Huang and Dr. G. Siuzdak for NMR spectroscopic and mass spectrometric assistance, respectively. Financial support for this work was provided by The Skaggs Institute for Chemical Biology, the National Institutes of Health (USA), a predoctoral fellowship from Bristol-Myers Squibb (F.B.), postdoctoral fellowships from the Academy of Finland, the Ella and Georg Ehrnrooth Foundation, and the Tauno Tönning Foundation (all to P.M.P.), ArrayBiopharma (N.Z.), and Bayer AG (N.D.), and grants from Abbott, Amgen, ArrayBiopharma, Boehringer-Ingelheim, Glaxo, Hoffmann-LaRoche, DuPont, Merck, Novartis, Pfizer, and Schering Plough. [electronic resource] by
Publication details: Angewandte Chemie (International ed. in English) Apr 2001
In:
Angewandte Chemie (International ed. in English) vol. 40
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299907.
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299908.
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299909.
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Nucleophilic Trapping of pi-Allylpalladium Intermediates Generated by Carbopalladation of Bicyclopropylidene: A Novel Three-Component Reaction Cyclopropyl Building Blocks in Organic Synthesis, Part 73. This work was supported by the Fonds der Chemischen Industrie and Bayer AG. We are indebted to Dr. B. Knieriem, Göttingen, for his careful proofreading of the final manuscript. Part 72: A. de Meijere, M. von Seebach, S. I. Kozhushkov, S. Cicchi, T. Dimoulas, A. Brandi, Eur. J. Org. Chem. 2001, in press; Part 71: A. de Meijere, S. I. Kozhushkov, D. Faber, V. Bagutskii, R. Boese, T. Haumann, R. Walsh, Eur. J. Org. Chem. 2001, in press. [electronic resource] by
Publication details: Angewandte Chemie (International ed. in English) Sep 2001
In:
Angewandte Chemie (International ed. in English) vol. 40
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299910.
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299911.
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299912.
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299913.
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1,2-Seleno Migrations in Carbohydrate Chemistry: Solution and Solid-Phase Synthesis of 2-Deoxy Glycosides, Orthoesters, and Allyl Orthoesters We thank Drs. D. H. Huang and G. Siuzdak for NMR spectroscopic and mass spectrometric assistance, respectively. We gratefully thank Nicolas Winssinger for helpful discussions and preparation of the selenium bromide resin. This work was financially supported by the Skaggs Institute for Chemical Biology, the National Institutes of Health (USA), postdoctoral fellowships from M.E.C., Spain (R.M.R., Fullbright), the Japan Society for the Promotion of Science (H.S.), the George Hewitt Foundation (K.C.F.), and grants from Schering Plough, Pfizer, Glaxo, Merck, Hoffmann - La Roche, DuPont, Abbott Laboratories, and Boehringer - Ingelheim. [electronic resource]
Publication details: Angewandte Chemie (International ed. in English) Mar 2000
In:
Angewandte Chemie (International ed. in English) vol. 39
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299914.
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299915.
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299916.
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299917.
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Model Studies towards Diazonamide A: Synthesis of the Heterocyclic Core We thank Dr. D. H. Huang, Dr. G. Suizdak, and Dr. R. Chadha for NMR spectroscopic, mass spectrometric, and X-ray crystallographic assistance, respectively. We also thank Professor R. H. Grubbs for a generous gift of catalyst 30. Financial support for this work was provided by The Skaggs Institute for Chemical Biology, the National Institutes of Health (USA), a predoctoral fellowship from the National Science Foundation (S.A.S.), postdoctoral fellowships from the Alfred Benzons Foundation and the Danish Natural Science Research Council (K.B.S.), and grants from Abbott, Amgen, ArrayBiopharma, Boehringer-Ingelheim, GlaxoWellcome, Hoffmann-LaRoche, DuPont, Merck, Novartis, Pfizer, and Schering Plough. [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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299918.
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299919.
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Synthesis of the ABCD Ring System of Azaspiracid We thank Drs. D. H. Huang and G. Siuzdak for NMR spectroscopic and mass spectrometric assistance, respectively. This work was financially supported by the National Institutes of Health (USA), The Skaggs Institute for Chemical Biology, a predoctoral fellowship from Bristol-Myers Squibb (to F.B.), postdoctoral fellowships from The Skaggs Institute for Research (to W.Q.), the Academy of Finland, the Ella and Georg Ehrnrooth Foundation and the Tauno Tönning Foundation (all to P.M.P.), and Bayer AG (to J.H.), as well as grants from Abbott, Amgen, ArrayBiopharma, Boehringer-Ingelheim, Glaxo, Hoffmann-La Roche, DuPont, Merck, Novartis, Pfizer, and Schering Plough. [electronic resource] by
Publication details: Angewandte Chemie (International ed. in English) Nov 2001
In:
Angewandte Chemie (International ed. in English) vol. 40
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299920.
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