标题
Gold Catalysis in Micellar Systems
作者
关键词
-
出版物
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
Volume 50, Issue 34, Pages 7820-7823
出版商
Wiley
发表日期
2011-07-02
DOI
10.1002/anie.201101396
参考文献
相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。- Gold-Catalyzed Nucleophilic Cyclization of Functionalized Allenes: A Powerful Access to Carbo- and Heterocycles
- (2011) Norbert Krause et al. CHEMICAL REVIEWS
- Manipulating Micellar Environments for Enhancing Transition Metal-Catalyzed Cross-Couplings in Water at Room Temperature
- (2011) Bruce H. Lipshutz et al. JOURNAL OF ORGANIC CHEMISTRY
- TPGS-750-M: A Second-Generation Amphiphile for Metal-Catalyzed Cross-Couplings in Water at Room Temperature
- (2011) Bruce H. Lipshutz et al. JOURNAL OF ORGANIC CHEMISTRY
- Recent Advances in Asymmetric Gold Catalysis
- (2010) Sujata Sengupta et al. ChemCatChem
- Stereoselective Negishi-like Couplings Between Alkenyl and Alkyl Halides in Water at Room Temperature
- (2010) Arkady Krasovskiy et al. ORGANIC LETTERS
- Combined coinage metal catalysis for the synthesis of bioactive molecules
- (2010) Norbert Krause et al. PURE AND APPLIED CHEMISTRY
- Gold and platinum catalysis—a convenient tool for generating molecular complexity
- (2009) Alois Fürstner CHEMICAL SOCIETY REVIEWS
- Silver and Gold Catalysis for Cycloisomerization Reactions
- (2009) Philippe Belmont et al. EUROPEAN JOURNAL OF ORGANIC CHEMISTRY
- Towards sustainable homogeneous gold catalysis: cycloisomerization of functionalized allenes in water
- (2009) Christian Winter et al. GREEN CHEMISTRY
- AllylicEthersas Educts for Suzuki−Miyaura Couplings in Water at Room Temperature
- (2009) Takashi Nishikata et al. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
- Zn-Mediated, Pd-Catalyzed Cross-Couplings in Water at Room TemperatureWithoutPrior Formation of Organozinc Reagents
- (2009) Arkady Krasovskiy et al. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
- PQS-2: ring-closing- and cross-metathesis reactions on lipophilic substrates; in water only at room temperature, with in-flask catalyst recycling
- (2009) Bruce H. Lipshutz et al. TETRAHEDRON
- Gold-Catalyzed Synthesis of 2,5-Dihydrofurans in Ionic Liquids
- (2008) Özge Aksιn et al. ADVANCED SYNTHESIS & CATALYSIS
- Ring-Closing Metathesis at Room Temperature within Nanometer Micelles using Water as the Only Solvent
- (2008) Bruce H. Lipshutz et al. ADVANCED SYNTHESIS & CATALYSIS
- Coinage Metal-Assisted Synthesis of Heterocycles
- (2008) Nitin T. Patil et al. CHEMICAL REVIEWS
- Gold-Catalyzed Organic Transformations
- (2008) Zigang Li et al. CHEMICAL REVIEWS
- Ligand Effects in Homogeneous Au Catalysis
- (2008) David J. Gorin et al. CHEMICAL REVIEWS
- Alternative Synthetic Methods through New Developments in Catalysis by Gold
- (2008) Antonio Arcadi CHEMICAL REVIEWS
- Gold-Catalyzed Cycloisomerizations of Enynes: A Mechanistic Perspective
- (2008) Eloísa Jiménez-Núñez et al. CHEMICAL REVIEWS
- Recent Developments in Enantioselective Gold(I) Catalysis
- (2008) Ross A. Widenhoefer CHEMISTRY-A EUROPEAN JOURNAL
- Room-Temperature Suzuki−Miyaura Couplings in Water Facilitated by Nonionic Amphiphiles†
- (2008) Bruce H. Lipshutz et al. ORGANIC LETTERS
- Heck Couplings at Room Temperature in Nanometer Aqueous Micelles†
- (2008) Bruce H. Lipshutz et al. ORGANIC LETTERS
- Micellar Catalysis of Suzuki−Miyaura Cross-Couplings with Heteroaromatics in Water
- (2008) Bruce H. Lipshutz et al. ORGANIC LETTERS
- Olefin Cross-Metathesis Reactions at Room Temperature Using the Nonionic Amphiphile “PTS”: Just Add Water†
- (2008) Bruce H. Lipshutz et al. ORGANIC LETTERS
- Golden opportunities in catalysis
- (2008) Norbert Krause et al. PURE AND APPLIED CHEMISTRY
- Gold-catalyzed reactions of C–H bonds
- (2008) Rachid Skouta et al. TETRAHEDRON
- Gold-catalysed reactions of alcohols: isomerisation, inter- and intramolecular reactions leading to C–C and C–heteroatom bonds
- (2008) Jacques Muzart TETRAHEDRON
Find the ideal target journal for your manuscript
Explore over 38,000 international journals covering a vast array of academic fields.
SearchAsk a Question. Answer a Question.
Quickly pose questions to the entire community. Debate answers and get clarity on the most important issues facing researchers.
Get Started