Direct Preparation of Key Intermediates in Heterocycle Synthesis Employing Novel Pd-Catalyzed Alpha-Arylation
采用新型 Pd 催化 α-芳基化直接制备杂环合成中的关键中间体
基本信息
- 批准号:428983-2011
- 负责人:
- 金额:$ 1.78万
- 依托单位:
- 依托单位国家:加拿大
- 项目类别:Engage Grants Program
- 财政年份:2011
- 资助国家:加拿大
- 起止时间:2011-01-01 至 2012-12-31
- 项目状态:已结题
- 来源:
- 关键词:
项目摘要
The majority of pharmaceutical compounds derive their beneficial properties from the presence of a
大多数药物化合物的有益性质来自于它们的药学上可接受的盐的存在。
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)
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Stradiotto, Mark其他文献
Palladium-catalyzed synthesis of indoles via ammonia cross-coupling-alkyne cyclization
- DOI:
10.1039/c1cc11874a - 发表时间:
2011-01-01 - 期刊:
- 影响因子:4.9
- 作者:
Alsabeh, Pamela G.;Lundgren, Rylan J.;Stradiotto, Mark - 通讯作者:
Stradiotto, Mark
Sequential one-pot three-step synthesis of polysubstituted 4-(5-(trifluoromethyl)-1H-pyrazol-4-yl)-1H-1,2,3-triazole systems
- DOI:
10.1039/c7ra07960e - 发表时间:
2017-01-01 - 期刊:
- 影响因子:3.9
- 作者:
Bonacorso, Helio G.;Dal Forno, Gean M.;Stradiotto, Mark - 通讯作者:
Stradiotto, Mark
Intramolecular Hydroamination of Unactivated Alkenes with Secondary Alkyl- and Arylamines Employing [Ir(COD)Cl]2 as a Catalyst Precursor
- DOI:
10.1021/ol900174f - 发表时间:
2009-03-19 - 期刊:
- 影响因子:5.2
- 作者:
Hesp, Kevin D.;Stradiotto, Mark - 通讯作者:
Stradiotto, Mark
A P,N-Ligand for Palladium-Catalyzed Ammonia Arylation: Coupling of Deactivated Aryl Chlorides, Chemoselective Arylations, and Room Temperature Reactions
- DOI:
10.1002/anie.201000526 - 发表时间:
2010-01-01 - 期刊:
- 影响因子:16.6
- 作者:
Lundgren, Rylan J.;Peters, Brendan D.;Stradiotto, Mark - 通讯作者:
Stradiotto, Mark
[Ir(COD)Cl]2 as a Catalyst Precursor for the Intramolecular Hydroamination of Unactivated Alkenes with Primary Amines and Secondary Alkyl- or Arylamines: A Combined Catalytic, Mechanistic, and Computational Investigation
- DOI:
10.1021/ja908316n - 发表时间:
2010-01-13 - 期刊:
- 影响因子:15
- 作者:
Hesp, Kevin D.;Tobisch, Sven;Stradiotto, Mark - 通讯作者:
Stradiotto, Mark
Stradiotto, Mark的其他文献
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{{ truncateString('Stradiotto, Mark', 18)}}的其他基金
Innovations in Cross-coupling via Mechanistically Guided Base-Metal Catalyst Design
通过机械引导的贱金属催化剂设计实现交叉偶联创新
- 批准号:
RGPIN-2019-04288 - 财政年份:2022
- 资助金额:
$ 1.78万 - 项目类别:
Discovery Grants Program - Individual
Exploiting Nickel Cross-coupling Catalysis for the Practical Synthesis and Functionalization of Pharmaceutically Relevant Organic Molecules
利用镍交叉偶联催化进行药物相关有机分子的实际合成和功能化
- 批准号:
561675-2021 - 财政年份:2021
- 资助金额:
$ 1.78万 - 项目类别:
Alliance Grants
Innovations in Cross-coupling via Mechanistically Guided Base-Metal Catalyst Design
通过机械引导的贱金属催化剂设计实现交叉偶联创新
- 批准号:
RGPIN-2019-04288 - 财政年份:2021
- 资助金额:
$ 1.78万 - 项目类别:
Discovery Grants Program - Individual
The pursuit of an expedient route to a proprietary agrochemical intermediate based on chemoselective metal-catalyzed alpha arylation
寻求基于化学选择性金属催化α芳基化的专有农用化学中间体的便捷途径
- 批准号:
566272-2021 - 财政年份:2021
- 资助金额:
$ 1.78万 - 项目类别:
Alliance Grants
Innovations in Cross-coupling via Mechanistically Guided Base-Metal Catalyst Design
通过机械引导的贱金属催化剂设计实现交叉偶联创新
- 批准号:
RGPIN-2019-04288 - 财政年份:2020
- 资助金额:
$ 1.78万 - 项目类别:
Discovery Grants Program - Individual
Nickel-Catalyzed Synthesis and N-Arylation of Biologically Active Sulfonamides
镍催化生物活性磺酰胺的合成和 N-芳基化
- 批准号:
542827-2019 - 财政年份:2019
- 资助金额:
$ 1.78万 - 项目类别:
Engage Grants Program
Innovations in Cross-coupling via Mechanistically Guided Base-Metal Catalyst Design
通过机械引导的贱金属催化剂设计实现交叉偶联创新
- 批准号:
RGPIN-2019-04288 - 财政年份:2019
- 资助金额:
$ 1.78万 - 项目类别:
Discovery Grants Program - Individual
Advancing Late Metal Catalysis: DalPhos Ligand Design, Mechanism, and New Reactivity
推进晚期金属催化:DalPhos 配体设计、机制和新反应性
- 批准号:
RGPIN-2014-04807 - 财政年份:2018
- 资助金额:
$ 1.78万 - 项目类别:
Discovery Grants Program - Individual
Advancing Late Metal Catalysis: DalPhos Ligand Design, Mechanism, and New Reactivity
推进晚期金属催化:DalPhos 配体设计、机制和新反应性
- 批准号:
RGPIN-2014-04807 - 财政年份:2017
- 资助金额:
$ 1.78万 - 项目类别:
Discovery Grants Program - Individual
Advancing Late Metal Catalysis: DalPhos Ligand Design, Mechanism, and New Reactivity
推进晚期金属催化:DalPhos 配体设计、机制和新反应性
- 批准号:
RGPIN-2014-04807 - 财政年份:2016
- 资助金额:
$ 1.78万 - 项目类别:
Discovery Grants Program - Individual
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