• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利：CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法，用中文像聊天一样搜索，搜遍4000万医学文献。AI智能推荐，让科研检索更轻松。

立即免费搜索

文件翻译

保留排版，准确专业，支持PDF/Word/PPT等文件格式，支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述，25分钟生成高质量综述，智能提取关键信息，辅助科研写作。

立即免费体验

CH.O Hydrogen Bonding Influences pi-Facial Stereoselective Epoxidations We are grateful to the National Institute of General Medical Sciences, National Institutes of Health (GM-36700) for financial support of this research and the National Computational Science Alliance (Illinois) for computer time and support.

作者信息

Washington Ilyas, Houk K. N.

机构信息

Department of Chemistry and Biochemistry University of California Los Angeles, CA 90095-1569 (USA).

出版信息

Angew Chem Int Ed Engl. 2001 Dec 3;40(23):4485-4488. doi: 10.1002/1521-3773(20011203)40:23<4485::aid-anie4485>3.0.co;2-n.

DOI:10.1002/1521-3773(20011203)40:23<4485::aid-anie4485>3.0.co;2-n
PMID:12404454
Abstract
摘要

相似文献

1
CH.O Hydrogen Bonding Influences pi-Facial Stereoselective Epoxidations We are grateful to the National Institute of General Medical Sciences, National Institutes of Health (GM-36700) for financial support of this research and the National Computational Science Alliance (Illinois) for computer time and support.氢键对π-面立体选择性环氧化反应的影响 我们感谢美国国立卫生研究院国家普通医学科学研究所（GM-36700）对本研究的资助，以及美国国家计算科学联盟（伊利诺伊州）提供的计算机机时和支持。
Angew Chem Int Ed Engl. 2001 Dec 3;40(23):4485-4488. doi: 10.1002/1521-3773(20011203)40:23<4485::aid-anie4485>3.0.co;2-n.
2
A Practical and Highly Efficient Aminohydroxylation of Unsaturated Carboxylic Acids We thank the National Institute of General Medical Sciences, the National Institutes of Health (GM 28384), National Science Foundation (CHE-9985553), and the W. M. Keck Foundation for financial support. We are also grateful to Prof. M. G. Finn, Dr. Wallace Pringle, and Dr. A. Erik Rubin for many helpful discussions.
Angew Chem Int Ed Engl. 2001 Sep 17;40(18):3455-3457. doi: 10.1002/1521-3773(20010917)40:18<3455::aid-anie3455>3.0.co;2-i.
3
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.
4
Insights into the Branched-Chain Formation of Mycarose: Methylation Catalyzed by an (S)-Adenosylmethionine-Dependent Methyltransferase We are grateful to Dr. Eugene Seno and the Lilly Research Laboratories for their generous gift of the plasmid pHJL311 and to the National Institutes of Health for grants (GM 35 906 and 54 346). H.-w.L. also thanks the National Institute of General Medical Sciences for a MERIT Award. T.M.H. was a trainee of the National Institute of General Medical Sciences (Biotechnology Training Grant: 2 T32 GM08347).对霉糖支链形成的见解：由依赖(S)-腺苷甲硫氨酸的甲基转移酶催化的甲基化 我们感谢尤金·塞诺博士和礼来研究实验室慷慨提供质粒pHJL311，也感谢美国国立卫生研究院提供的资助（GM 35906和54346）。H.-w.L.还感谢国立综合医学科学研究所授予的功绩奖。T.M.H.曾是国立综合医学科学研究所的一名受训人员（生物技术培训资助：2 T32 GM08347）。
Angew Chem Int Ed Engl. 2001 Feb 2;40(3):607-610.
5
Twenty five years of the National Academy of Medical Sciences of Ukraine - progress and priorities for future of radiation medicine and biology.乌克兰国家医学科学院的二十五年——放射医学与生物学的进展及未来优先事项
Probl Radiac Med Radiobiol. 2017 Dec;22:10-14.
6
First Example of the µ(3)-eta(1),eta(2),eta(1)-C(60) Bonding Mode: Ligand-Induced Conversion of pi to sigma C(60)-Metal Complexes We are grateful to the National Research Laboratory (NRL) Program of Korean Ministry of Science & Technology (MOST) and the Korea Science Engineering Foundation (Project No. 1999-1-122-001-5) for financial support of this research.μ(3)-η(1),η(2),η(1)-C(60)键合模式的首个实例：配体诱导的π到σ C(60)-金属配合物的转化 我们感谢韩国科学技术部（MOST）的国家研究实验室（NRL）计划以及韩国科学工程基金会（项目编号1999-1-122-001-5）对本研究的资金支持。
Angew Chem Int Ed Engl. 2001 Apr 17;40(8):1500-1502.
7
Synthesis of the First (1-3:6,7-eta-Cyclodecadienyl)ruthenium Complex by the Intramolecular Reaction of an Alkene and a Vinylcyclopropane We thank the National Science Foundation and the National Institutes of Health (NIH), General Medical Sciences, for their generous support of our programs. We are grateful to A. Cole for solving the X-ray structure of 3. Mass spectra were provided by the Mass Spectrometry Facility of the University of California, San Francisco, supported by the NIH Division of Research Resources.通过烯烃与乙烯基环丙烷的分子内反应合成首例（1-3:6,7-η-环癸二烯基）钌配合物 我们感谢美国国家科学基金会以及美国国立卫生研究院（NIH）普通医学科学部对我们研究项目的慷慨支持。我们感谢A. 科尔解析了3的X射线晶体结构。质谱由加利福尼亚大学旧金山分校质谱分析设施提供，该设施得到了NIH研究资源司的支持。
Angew Chem Int Ed Engl. 2001 Mar 16;40(6):1114-1116. doi: 10.1002/1521-3773(20010316)40:6<1114::aid-anie11140>3.0.co;2-x.
8
DesVI: A New Member of the Sugar N,N-Dimethyltransferase Family Involved in the Biosynthesis of Desosamine The authors gratefully acknowledge financial support provided by the National Institutes of Health (GM 54346). H.-w.L. also thanks the National Institute of General Medical Sciences for a MERIT Award. L.Z. is the recipient of a Graduate School Dissertation Fellowship from the University of Minnesota.去氧氨基糖糖基N，N-二甲基转移酶家族的新成员DesVI参与去氧氨基糖的生物合成。作者衷心感谢美国国立卫生研究院（GM 54346）提供的资金支持。H.-w.L.也感谢国立综合医学科学研究所授予的优秀科研奖。L.Z.获得了明尼苏达大学研究生院的博士论文奖学金。
Angew Chem Int Ed Engl. 2000 Jun 16;39(12):2160-2163. doi: 10.1002/1521-3773(20000616)39:12<2160::aid-anie2160>3.0.co;2-e.
9
Decoding Products of Diversity Pathways from Stock Solutions Derived from Single Polymeric Macrobeads H.E.B. and L.P. contributed equally to this work. We thank the National Institute of General Medical Sciences (GM-52067) for the support of this research. We are especially grateful to Dr. Andrew Tyler for expert mass spectroscopy support. The Harvard ICCB is supported by Merck & Co., Merck KGaA, the Keck Foundation, and the National Cancer Institute. H.E.B. is supported by a postdoctoral fellowship from the Jane Coffin Childs Memorial Fund for Medical Research (sponsored by Merck & Co.). L.P. is a Research Fellow, and S.L.S. is an Investigator with the Howard Hughes Medical Institute at the Department of Chemistry and Chemical Biology, Harvard University.从单个聚合物大珠衍生的储备溶液中解码多样性途径的产物 H.E.B. 和 L.P. 对本工作贡献相同。我们感谢美国国立综合医学科学研究所（GM - 52067）对本研究的支持。我们特别感谢 Andrew Tyler 博士提供的专业质谱分析支持。哈佛综合癌症研究中心由默克公司、默克集团、凯克基金会和美国国立癌症研究所提供支持。H.E.B. 获得简·科芬·蔡尔德斯医学研究纪念基金（由默克公司赞助）的博士后奖学金支持。L.P. 是一名研究员，S.L.S. 是哈佛大学化学与化学生物学系霍华德·休斯医学研究所的一名研究员。
Angew Chem Int Ed Engl. 2001 Sep 17;40(18):3421-3425. doi: 10.1002/1521-3773(20010917)40:18<3421::aid-anie3421>3.0.co;2-b.
10
A Mass Spectrometric Labeling Strategy for High-Throughput Reaction Evaluation and Optimization: Exploring C-H Activation This work was supported by the Director, Office of Energy Research, Office of Basic Energy Sciences, Chemical Sciences Division, U.S. Department of Energy, under contract No. DE-AC03-76SF00098. We are grateful to the National Institutes of Health for support (GM-50353) and for a Postdoctoral Fellowship to J.W.S.一种用于高通量反应评估与优化的质谱标记策略：探索C-H活化 本工作得到了美国能源部基础能源科学办公室化学科学司能源研究办公室主任的支持，合同编号为DE-AC03-76SF00098。我们感谢美国国立卫生研究院的支持（资助号GM-50353）以及授予J.W.S.的博士后奖学金。
Angew Chem Int Ed Engl. 2001 Jan 5;40(1):216-219.

引用本文的文献

1
Trialkylphosphonium oxoborates as C(sp)-H oxyanion holes and their application in catalytic chemoselective acetalization.作为C(sp)-H氧阴离子空穴的三烷基鏻氧硼酸酯及其在催化化学选择性缩醛化中的应用。
Chem Sci. 2023 Oct 20;14(44):12684-12692. doi: 10.1039/d3sc03081d. eCollection 2023 Nov 15.
2
Synthesis and characterization of privileged monodentate phosphoramidite ligands and chiral Brønsted acids derived from d-mannitol.源自d-甘露糖醇的特殊单齿亚磷酰胺配体和手性布朗斯特酸的合成与表征
Int J Mol Sci. 2012;13(3):2727-2743. doi: 10.3390/ijms13032727. Epub 2012 Feb 29.
3
Quantitative DFT modeling of the enantiomeric excess for dioxirane-catalyzed epoxidations.
二氧杂环丙烷催化环氧化对映体过量的定量密度泛函理论建模。
J Am Chem Soc. 2009 Mar 25;131(11):3965-73. doi: 10.1021/ja806951r.
4
Stereoselective epoxidation of 4-deoxypentenosides: a polarized-pi model.4-脱氧戊烯糖苷的立体选择性环氧化：一种极化π模型
Org Lett. 2006 Sep 28;8(20):4545-8. doi: 10.1021/ol0617401.
5
Origins of stereoselectivity in Diels-Alder cycloadditions catalyzed by chiral imidazolidinones.手性咪唑啉酮催化的狄尔斯-阿尔德环加成反应中立体选择性的起源
J Am Chem Soc. 2006 Mar 22;128(11):3543-53. doi: 10.1021/ja0525859.