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A Novel Concept in Combinatorial Chemistry in Solution with the Advantages of Solid-Phase Synthesis: Formation of N-Betaines by Multicomponent Domino Reactions This work was supported as part of the BMBF Project "Kombinatorische Chemie" (grant number 03 D0056 2). We thank BASF AG, Ludwigshafen, and the Fonds der Chemischen Industrie for generous support.

作者信息

Tietze Lutz F., Evers Holger, Töpken Enno

机构信息

Institut für Organische Chemie der Universität Tammannstrasse 2, 37077 Göttingen (Germany).

出版信息

Angew Chem Int Ed Engl. 2001 Mar 2;40(5):903-905.

PMID:11241641
Abstract
摘要

相似文献

1
A Novel Concept in Combinatorial Chemistry in Solution with the Advantages of Solid-Phase Synthesis: Formation of N-Betaines by Multicomponent Domino Reactions This work was supported as part of the BMBF Project "Kombinatorische Chemie" (grant number 03 D0056 2). We thank BASF AG, Ludwigshafen, and the Fonds der Chemischen Industrie for generous support.溶液中组合化学的一个具有固相合成优势的新概念：通过多组分多米诺反应形成N-甜菜碱 本研究作为德国联邦教育与研究部“组合化学”项目（资助编号03 D0056 2）的一部分得到支持。我们感谢路德维希港的巴斯夫股份公司和化学工业基金会的慷慨支持。
Angew Chem Int Ed Engl. 2001 Mar 2;40(5):903-905.
2
The First Stable Diazonium Ion on Solid Support-Investigations on Stability and Usage as Linker and Scavenger in Solid-Phase Organic Synthesis Nitrogen-Based Linkers, Part 8. This work was supported by the Fonds der Chemischen Industrie (Liebig-Stipend to S.B.) and the Deutsche Forschungsgemeinschaft (BR1750-1). We thank Prof. Dr. D. Enders for the generous support of our work. The companies BASF AG, Bayer AG, Degussa-Hüls AG, and Calbiochem-Novabiochem AG are acknowledged for donations of chemicals and Grünenthal GmbH for financial support. For DSC measurements we also thank Prof. Dr. Franz-Josef Wortmann and Dr. Numan Özgün at the Deutsches Wollforschungsinstitut (DWI) at the RWTH Aachen. Part 7: M. Lormann, S. Dahmen, S. Bräse, Tetrahedron Lett. 2000, 41, 3813-3816.
Angew Chem Int Ed Engl. 2000 Oct 16;39(20):3681-3683.
3
Versatile Indole Synthesis by a 5-endo-dig Cyclization Mediated by Potassium or Cesium Bases We thank the DFG (Leibniz-Programm) and the Fonds der Chemischen Industrie for generous financial support. A.L.R. and C. K. thank the Humboldt-Foundation and the BASF AG, respectively, for fellowships. W.D. was supported by the BMBF program (03 D 0056 2). We thank Dr. J. Henkelmann (BASF AG) for helpful discussions and the BASF AG for the generous gift of chemicals.
Angew Chem Int Ed Engl. 2000 Jul 17;39(14):2488-2490. doi: 10.1002/1521-3773(20000717)39:14<2488::aid-anie2488>3.0.co;2-e.
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Highly Diastereoselective Synthesis of Monocyclic and Bicyclic Secondary Diorganozinc Reagents with Defined Configuration We thank the DFG (SFB 260, Leibniz-Program) and the Fonds der Chemischen Industrie for generous support (Kekulé-scholarship for E. H.). We thank BASF, Degussa-Hüls AG, and Chemetall GmbH AG for the generous gift of chemicals.
Angew Chem Int Ed Engl. 2000 Jul 3;39(13):2294-2297.
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Dipolar Dye Aggregates: A Problem for Nonlinear Optics, but a Chance for Supramolecular Chemistry This work was supported by the Deutsche Forschungsgemeinschaft (Wu 317/1), the Fonds der Chemischen Industrie and BASF AG (travel grant for S.Y.). We thank Dr. Udo Werz for 2D NMR experiments and Prof. Peter Bäuerle for his support.
Angew Chem Int Ed Engl. 2000 Jun 2;39(11):1978-1981.
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Total Synthesis of the Macrolide Antibiotic 5,6-Dihydrocineromycin B This work was supported by the DFG (SFB 416) and the Fonds der Chemischen Industrie. We thank Prof. Dr. A. Zeeck for supplying data of the title compound, as well as BASF, Degussa-Hüls and Wacker-Chemie for donations of chemicals.大环内酯类抗生素5,6-二氢西奈霉素B的全合成 本研究得到德国研究基金会（SFB 416）和化学工业基金会的支持。我们感谢A. Zeeck教授提供标题化合物的数据，以及巴斯夫、德固赛-赫尔斯公司和瓦克化学公司捐赠的化学品。
Angew Chem Int Ed Engl. 2001 Mar 2;40(5):901-902.
7
Asymmetric Synthesis of alpha-Substituted beta-Nitrophosphonic Acids by Phospha-Analogous Michael Addition to Aromatic Nitroalkenes This work was supported by the Deutsche Forschungsgemeinschaft (Sonderforschungsbereich 380) and by the Fonds der Chemischen Industrie. We thank Jens Hasenjäger for his contribution to the experimental part of this work and the companies Degussa AG, BASF AG, and Bayer AG for the donation of chemicals.
Angew Chem Int Ed Engl. 2000 Dec 15;39(24):4605-4607.
8
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Angew Chem Int Ed Engl. 2001 May 18;40(10):1910-1913.
9
A New Strategy for Synthesizing Endohedral Metallocenophanes This work was supported by the Deutsche Forschungsgemeinschaft, the Fonds der Chemischen Industrie, and the BASF AG Ludwigshafen.合成内嵌金属茂套索烃的新策略 本研究得到了德国研究基金会、化学工业基金会以及路德维希港巴斯夫股份公司的支持。
Angew Chem Int Ed Engl. 2001 Jul 2;40(13):2477-2479.
10
First, Atropo-Enantioselective Total Synthesis of the Axially Chiral Phenylanthraquinone Natural Products Knipholone and 6'-O-Methylknipholone Novel Concepts in Directed Biaryl Synthesis, Part 93. This work was supported by the Deutsche Forschungsgemeinschaft (grant: SFB 347) and by the Fonds der Chemischen Industrie. We thank Prof. B. M. Abegaz und Dr. M. Bezabih for an authentic sample of 6'-O-methylknipholone and for valuable discussions. We thank J. Kraus for helpful suggestions and V. Barthel for technical support. Part 92: G. Bringmann, J. Hinrichs, K. Peters, E.-M. Peters, J. Org. Chem. 2001, 66, 629-632.首先，轴手性苯基蒽醌天然产物克尼佛隆和6'-O-甲基克尼佛隆的对映体选择性全合成：联芳基定向合成中的新概念，第93部分。这项工作得到了德国研究基金会（资助：SFB 347）和化学工业基金会的支持。我们感谢B. M. Abegaz教授和M. Bezabih博士提供6'-O-甲基克尼佛隆的真实样品以及进行的宝贵讨论。我们感谢J. Kraus提出的有益建议和V. Barthel提供的技术支持。第92部分：G. Bringmann、J. Hinrichs、K. Peters、E.-M. Peters，《有机化学杂志》2001年，66卷，629 - 632页。
Angew Chem Int Ed Engl. 2001 May 4;40(9):1687-1690.

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