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Isolation of an Acid/Base Complex in Solution Puts the Brakes on Nitrogen Inversion We are grateful for financial support from the Skaggs Research Foundation and the National Institutes of Health. We are pleased to acknowledge advice from Professors Stephen Craig and Dmitry Rudkevich.

作者信息

Wash Paul L., Renslo Adam R., Rebek Julius

机构信息

The Skaggs Institute for Chemical Biology and Department of Chemistry The Scripps Research Institute 10550 North Torrey Pines Road, La Jolla, CA 92037 (USA).

出版信息

Angew Chem Int Ed Engl. 2001 Apr 1;40(7):1221-1222.

PMID:11301430
Abstract
摘要

相似文献

1
Isolation of an Acid/Base Complex in Solution Puts the Brakes on Nitrogen Inversion We are grateful for financial support from the Skaggs Research Foundation and the National Institutes of Health. We are pleased to acknowledge advice from Professors Stephen Craig and Dmitry Rudkevich.溶液中酸碱配合物的分离抑制了氮的翻转 我们感谢斯卡格斯研究基金会和美国国立卫生研究院的资金支持。我们很高兴地感谢斯蒂芬·克雷格教授和德米特里·鲁德凯维奇教授的建议。
Angew Chem Int Ed Engl. 2001 Apr 1;40(7):1221-1222.
2
Molecular Recognition with Introverted Functionality We are grateful for financial support from the Skaggs Research Foundation and the National Institutes of Health. We thank Prof. Dmitry Rudkevich and Dr. Paul Wash and Dr. Laura Pasternack for helpful advice and instrumental support.
Angew Chem Int Ed Engl. 2000 Sep 15;39(18):3281-3283. doi: 10.1002/1521-3773(20000915)39:18<3281::aid-anie3281>3.0.co;2-p.
3
Nanoscale Container Structures and Their Host - Guest Properties We are grateful for financial support from the Skaggs Research Foundation and the National Institutes of Health. Dr. Laura Pasternack and Dr. Takeharu Haino are sincerely acknowledged for assistance with the 2D NMR experiments and experimental advise, respectively.
Angew Chem Int Ed Engl. 2000 Mar;39(6):1076-1079. doi: 10.1002/(sici)1521-3773(20000317)39:6<1076::aid-anie1076>3.0.co;2-e.
4
Solution and Solid-Phase Synthesis of Functionalized 3-Arylbenzofurans by a Novel Cyclofragmentation - Release Pathway Financial support for this work was provided by The Skaggs Institute for Chemical Biology, the National Institutes of Health (USA), doctoral fellowships from the National Science Foundation (S.A.S.) and the Department of Defense (J.A.P.), and grants from Abbott, Amgen, Boehringer - Ingelheim, Glaxo, Hoffmann - La Roche, DuPont, Merck, Novartis, Pfizer, and Schering Plough.通过新型环化断裂-释放途径实现功能化3-芳基苯并呋喃的溶液和固相合成 这项工作得到了斯卡格斯化学生物学研究所、美国国立卫生研究院、美国国家科学基金会（S.A.S.）的博士奖学金、美国国防部（J.A.P.）以及雅培、安进、勃林格殷格翰、葛兰素、霍夫曼-罗氏、杜邦、默克、诺华、辉瑞和先灵葆雅等公司的资助。
Angew Chem Int Ed Engl. 2000 Mar;39(6):1093-1096.
5
Mechanistic Studies of Periodinane-Mediated Reactions of Anilides and Related Systems Professors M. G. Finn, A. Eschenmoser, and M. E. Newcomb are gratefully acknowledged for valuable discussions and suggestions. We thank Dr. D. H. Huang and Dr. G. Siuzdak for NMR spectroscopic and mass spectrometric assistance, respectively. We would also like to thank Dr. G. Vasilikogiannakis for helpful discussions and an anonymous referee for critical suggestions. 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 (P.B.), postdoctoral fellowships from ArrayBiopharma (N.Z.) and Bayer AG (R.K.), and grants from Abbott, Amgen, ArrayBiopharma, Boehringer-Ingelheim, Glaxo, Hoffmann-LaRoche, DuPont, Merck, Novartis, Pfizer, and Schering Plough.高碘烷介导的酰苯胺及相关体系反应的机理研究 衷心感谢M. G. 芬恩教授、A. 埃申莫泽教授和M. E. 纽科姆教授进行的宝贵讨论并提出建议。我们分别感谢D. H. 黄博士和G. 苏兹达克博士在核磁共振光谱分析和质谱分析方面提供的帮助。我们还要感谢G. 瓦西利科贾纳基斯博士进行的有益讨论，以及一位匿名审稿人提出的批判性建议。这项工作得到了斯卡格斯化学生物学研究所、美国国立卫生研究院、美国国家科学基金会提供的博士前奖学金（P.B.）、ArrayBiopharma公司（N.Z.）和拜耳公司（R.K.）提供的博士后奖学金，以及雅培公司、安进公司、ArrayBiopharma公司、勃林格殷格翰公司、葛兰素公司、霍夫曼 - 罗氏公司、杜邦公司、默克公司、诺华公司、辉瑞公司和先灵葆雅公司提供的资助。
Angew Chem Int Ed Engl. 2001 Jan 5;40(1):202-206.
6
[80 years' of internal medicine education at the medical school of the university in Belgrade (1922-2002)].[贝尔格莱德大学医学院的内科医学教育80年（1922 - 2002）]
Srp Arh Celok Lek. 2003 Jul-Aug;131(7-8):351-64.
7
Dehydrogenative Dimerization of Tin Hydrides Catalyzed by Ruthenium-Allenylidene Complexes We thank The Skaggs Institute for Chemical Biology at The Scripps Research Institute for support of this work; S.M.M. is a Skaggs Postdoctoral Fellow. We are also grateful to Dr. Michal Sabat (University of Virginia) for X-ray crystallography and Prof. David Goodin (The Scripps Research Institute) for the EPR experiment described in ref. 14.钌-亚联烯基配合物催化氢化锡的脱氢二聚反应 我们感谢斯克里普斯研究所的斯卡格斯化学生物学研究所对本工作的支持；S.M.M. 是斯卡格斯博士后研究员。我们还感谢弗吉尼亚大学的Michal Sabat博士进行X射线晶体学研究，以及斯克里普斯研究所的David Goodin教授进行参考文献14中描述的电子顺磁共振实验。
Angew Chem Int Ed Engl. 2001 Jun 1;40(11):2138-2141.
8
Tandem Intramolecular Alkyne Silylformylation-Allylsilylation: A Case of Remote 1,5-Asymmetric Induction Financial support was provided by the National Institutes of Health (National Institute of General Medical Sciences, GM58133). We are grateful to Bristol-Myers Squibb for generous financial support in the form of an Unrestricted Grant in Synthetic Organic Chemistry to J.L.L. We thank Merck Research Laboratories and DuPont Pharmaceuticals for generous financial support.
Angew Chem Int Ed Engl. 2001 Aug 3;40(15):2915-2917.
9
New Synthetic Technology for the Construction of N-Containing Quinones and Derivatives Thereof: Total Synthesis of Epoxyquinomycin B We thank Dr. D. H. Huang, Dr. G. Siuzdak, and Dr. R. Chadha for NMR spectroscopic, mass spectrometric, and X-ray crystallographic 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 the National Science Foundation (P.B.), and grants from Abbott, Amgen, ArrayBiopharma, Boehringer-Ingelheim, Glaxo, Hoffmann-LaRoche, DuPont, Merck, Novartis, Pfizer, and Schering Plough.含氮醌类化合物及其衍生物构建的新型合成技术：环氧喹诺霉素B的全合成 我们分别感谢D. H. Huang博士、G. Siuzdak博士和R. Chadha博士在核磁共振光谱、质谱和X射线晶体学分析方面提供的帮助。本研究得到了斯卡格斯化学生物学研究所、美国国立卫生研究院的资助，国家科学基金会提供的博士前奖学金（P.B.），以及雅培、安进、Array生物制药、勃林格殷格翰、葛兰素史克、霍夫曼 - 罗氏、杜邦、默克、诺华、辉瑞和先灵葆雅公司的资助。
Angew Chem Int Ed Engl. 2001 Jan 5;40(1):207-210.
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Angew Chem Int Ed Engl. 2001 May 4;40(9):1573.

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