Career: Catalytic, Enantioselective C-C Bond Forming Reactions of Imines
职业:亚胺的催化、对映选择性 C-C 键形成反应
基本信息
- 批准号:9874694
- 负责人:
- 金额:$ 27.2万
- 依托单位:
- 依托单位国家:美国
- 项目类别:Standard Grant
- 财政年份:1999
- 资助国家:美国
- 起止时间:1999-02-01 至 2003-01-31
- 项目状态:已结题
- 来源:
- 关键词:
项目摘要
Professor Leckta's multifaceted research efforts explore aspects of asymmetric transformations of imines. These include addition reactions of enol- and allylsilanes and ketene silyl acetals to imino esters catalyzed by chiral Lewis acids, asymmetric Staudinger and Baylis-Hillman reactions. Also, the development of novel catalysts based on diborane as a bifunctional Lewis acid and (bis)phosphine ligands is being pursued while incorporating computations to evaluate and possibly design useful catalytic species. Creating a bridge between the experimental and the theoretical is a hallmark of Professor Leckta'a teaching goals, with computational chemistry employed in the introductory as well as advanced aspects of his curriculum. Further, plans are being made to include high school teachers with one goal being to develop visual aids to pique the interest of high school students.With this CAREER award, the Synthetic Organic Program supports the research and teaching efforts of Dr. Thomas Leckta of Johns Hopkins University. Professor Leckta's research deals with new ways to make nitrogen-containing molecules called amines in such a way that the three- dimensional shape or chirality of the molecule is controlled. This is ever more important when designing the synthesis of biomolecules and drugs. Professor Leckta's teaching emphasizes the use of computers as a tool for predicting the outcome of chemical reactions before time is invested in actually trying the chemistry in the laboratory. An outreach program is being planned that will involve high school teachers and provide demonstrations of high-quality graphics and computations to high school students.
Leckta 教授的多方面研究工作探索了亚胺不对称转化的各个方面。 这些包括由手性路易斯酸催化的烯醇硅烷和烯丙基硅烷以及烯酮甲硅烷基缩醛与亚氨基酯的加成反应、不对称施陶丁格反应和贝利斯-希尔曼反应。 此外,人们正在开发基于乙硼烷作为双功能路易斯酸和(双)膦配体的新型催化剂,同时结合计算来评估和可能设计有用的催化物质。 在实验和理论之间架起一座桥梁是莱克塔教授教学目标的一个标志,他的课程的入门和高级部分都采用了计算化学。 此外,我们还计划将高中教师纳入其中,目标之一是开发视觉教具以激发高中生的兴趣。通过这一职业奖,合成有机项目支持约翰·霍普金斯大学托马斯·莱克塔博士的研究和教学工作。 莱克塔教授的研究涉及制造称为胺的含氮分子的新方法,其方式是控制分子的三维形状或手性。 在设计生物分子和药物的合成时,这一点变得更加重要。 莱克塔教授的教学强调在投入时间在实验室中实际尝试化学反应之前,使用计算机作为预测化学反应结果的工具。 正在计划一项外展计划,该计划将邀请高中教师参与,并向高中生提供高质量图形和计算的演示。
项目成果
期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
数据更新时间:{{ journalArticles.updateTime }}
{{
item.title }}
{{ item.translation_title }}
- DOI:
{{ item.doi }} - 发表时间:
{{ item.publish_year }} - 期刊:
- 影响因子:{{ item.factor }}
- 作者:
{{ item.authors }} - 通讯作者:
{{ item.author }}
数据更新时间:{{ journalArticles.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ monograph.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ sciAawards.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ conferencePapers.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ patent.updateTime }}
Thomas Lectka其他文献
The reaction of aluminum cluster anions with tetrakis(dimethylamino)ethylene (TDMAE): Insertion of an aluminum anion into a C–N bond
- DOI:
10.1016/j.cplett.2009.09.101 - 发表时间:
2009-10-28 - 期刊:
- 影响因子:
- 作者:
Xiang Li;Andrej Grubisic;Soren Eustis;Di Wang;Thomas Lectka;Gerd F. Ganteför;Kit H. Bowen;R. Burgert;H. Schnöckel - 通讯作者:
H. Schnöckel
Can the −CFsub3/sub Group Act as a Tight, Well-Defined Hydrogen Bond Acceptor? A Clear Crystallographic CFsub2/sub–F···H–Nsup+/sup Interaction Says Yes
- CF3 基团能否充当紧密、定义明确的氢键受体?一个清晰的晶体学 CF2-F···H+N+相互作用表明是肯定的。
- DOI:
10.1021/acs.joc.4c00873 - 发表时间:
2024-07-05 - 期刊:
- 影响因子:3.600
- 作者:
Muyuan Wang;Nathaniel Garrison;Phuong Minh Nguyen;Aarush Prasad;Yuang Wang;Hyeok-Kyu Kwon;Gina Kim;Maxime A. Siegler;Thomas Lectka - 通讯作者:
Thomas Lectka
The close interaction of a C<img class="glyph" src="https://sdfestaticassets-us-east-1.sciencedirectassets.com/shared-assets/16/entities/sbnd" />F bond with a carbonyl π–system: Attractive, repulsive, or both?
- DOI:
10.1016/j.jfluchem.2016.06.016 - 发表时间:
2016-08-01 - 期刊:
- 影响因子:
- 作者:
Maxwell Gargiulo Holl;Mark D. Struble;Maxime A. Siegler;Thomas Lectka - 通讯作者:
Thomas Lectka
A highly selective C–H bond fluorination unlocks conformational reporting in a complex natural product derivative
一种高选择性的 C-H 键氟化作用揭示了一种复杂天然产物衍生物中的构象报告。
- DOI:
10.1039/d5sc01857a - 发表时间:
2025-04-10 - 期刊:
- 影响因子:7.400
- 作者:
Jonah Ruskin;Roxanne Dekeyser;Nathaniel Garrison;Phoebe Williams;Maya Kramer-Johansen;Ananya Majumdar;Travis Dudding;Adam Huczyński;Thomas Lectka - 通讯作者:
Thomas Lectka
The C<img class="glyph" src="https://sdfestaticassets-us-east-1.sciencedirectassets.com/shared-assets/16/entities/sbnd" />F⋅⋅⋅H<img class="glyph" src="https://sdfestaticassets-us-east-1.sciencedirectassets.com/shared-assets/16/entities/sbnd" />CF<sub>2</sub> interaction: A combination of hydrogen bonding and <em>n</em> → <em>σ</em>* stabilization
- DOI:
10.1016/j.jfluchem.2023.110191 - 发表时间:
2023-11-01 - 期刊:
- 影响因子:
- 作者:
Nathaniel G. Garrison;Stefan Andrew Harry;Maxime A. Siegler;Guilherme Cariello;Rodrigo A. Cormanich;Thomas Lectka - 通讯作者:
Thomas Lectka
Thomas Lectka的其他文献
{{
item.title }}
{{ item.translation_title }}
- DOI:
{{ item.doi }} - 发表时间:
{{ item.publish_year }} - 期刊:
- 影响因子:{{ item.factor }}
- 作者:
{{ item.authors }} - 通讯作者:
{{ item.author }}
{{ truncateString('Thomas Lectka', 18)}}的其他基金
Two Complementary Approaches to Site-Selective HAT and ET Reactions
位点选择性 HAT 和 ET 反应的两种互补方法
- 批准号:
2350270 - 财政年份:2024
- 资助金额:
$ 27.2万 - 项目类别:
Standard Grant
Lewis Base Directed Intermolecular Hydrogen Atom Transfer
路易斯碱定向分子间氢原子转移
- 批准号:
2102116 - 财政年份:2021
- 资助金额:
$ 27.2万 - 项目类别:
Standard Grant
New Approaches to Site-Selective Fluorination
位点选择性氟化的新方法
- 批准号:
1800510 - 财政年份:2018
- 资助金额:
$ 27.2万 - 项目类别:
Continuing Grant
New Approaches to Site-Selective Fluorination
位点选择性氟化的新方法
- 批准号:
1465131 - 财政年份:2015
- 资助金额:
$ 27.2万 - 项目类别:
Standard Grant
Polycomponent Catalysis in Organic Synthesis
有机合成中的多组分催化
- 批准号:
1152996 - 财政年份:2012
- 资助金额:
$ 27.2万 - 项目类别:
Standard Grant
Activation of C-F Bonds by Aryl Carbocations
芳基碳阳离子活化 C-F 键
- 批准号:
9809433 - 财政年份:1998
- 资助金额:
$ 27.2万 - 项目类别:
Continuing Grant
相似海外基金
Catalytic Enantioselective Strain Release For The Synthesis Of Chiral Cycloalkanes
催化对映选择性应变释放用于合成手性环烷烃
- 批准号:
EP/Y02687X/1 - 财政年份:2024
- 资助金额:
$ 27.2万 - 项目类别:
Fellowship
New Catalytic Enantioselective Desymmetrisation Reactions
新的催化对映选择性去对称反应
- 批准号:
2890599 - 财政年份:2023
- 资助金额:
$ 27.2万 - 项目类别:
Studentship
Catalytic enantioselective synthesis of non-centrochiral compounds using aryne intermediate
使用芳炔中间体催化对映选择性合成非中心手性化合物
- 批准号:
22H02081 - 财政年份:2022
- 资助金额:
$ 27.2万 - 项目类别:
Grant-in-Aid for Scientific Research (B)
New Enantioselective Catalytic Desymmetrisation Reactions
新的对映选择性催化去对称反应
- 批准号:
2446223 - 财政年份:2020
- 资助金额:
$ 27.2万 - 项目类别:
Studentship
Enantioselective Catalytic Chlorosilane Reactions
对映选择性催化氯硅烷反应
- 批准号:
10046812 - 财政年份:2020
- 资助金额:
$ 27.2万 - 项目类别:
CAREER: Development of catalytic enantioselective hydrofunctionalizations of alkenes
职业:烯烃催化对映选择性氢官能化的发展
- 批准号:
1848076 - 财政年份:2019
- 资助金额:
$ 27.2万 - 项目类别:
Continuing Grant
A General Co-Catalytic Methodology for Enantioselective Photoredox Radical Cation Reactions
对映选择性光氧化还原自由基阳离子反应的通用助催化方法
- 批准号:
10001979 - 财政年份:2019
- 资助金额:
$ 27.2万 - 项目类别:
A General Co-Catalytic Methodology for Enantioselective Photoredox Radical Cation Reactions
对映选择性光氧化还原自由基阳离子反应的通用助催化方法
- 批准号:
10241313 - 财政年份:2019
- 资助金额:
$ 27.2万 - 项目类别:
Catalytic Enantioselective 1,2-Rearrangements Using Lewis Base Catalysis
使用路易斯碱催化的催化对映选择性 1,2-重排
- 批准号:
2104946 - 财政年份:2018
- 资助金额:
$ 27.2万 - 项目类别:
Studentship
Development of Catalytic Enantioselective Intermolecular Diene Hydrofunctionalization Reactions
催化对映选择性分子间二烯氢官能化反应的进展
- 批准号:
1800012 - 财政年份:2018
- 资助金额:
$ 27.2万 - 项目类别:
Standard Grant














{{item.name}}会员




