Synthesis of Spirooxindoles from Carbamoyl Chlorides via Cyclopropyl Methine C(sp3)–H Activation Using Palladium Catalyst
Published 2013 View Full Article
- Home
- Publications
- Publication Search
- Publication Details
Title
Synthesis of Spirooxindoles from Carbamoyl Chlorides via Cyclopropyl Methine C(sp3)–H Activation Using Palladium Catalyst
Authors
Keywords
-
Journal
CHEMISTRY LETTERS
Volume 42, Issue 7, Pages 753-755
Publisher
The Chemical Society of Japan
Online
2013-05-28
DOI
10.1246/cl.130228
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- Palladium(0)-Catalyzed Alkynylation of C(sp3)–H Bonds
- (2013) Jian He et al. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
- Palladium-Catalyzed Picolinamide-Directed Alkylation of Unactivated C(sp3)–H Bonds with Alkyl Iodides
- (2013) Shu-Yu Zhang et al. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
- Synthesis of Functionalized Spiroindolines via Palladium-Catalyzed Methine C–H Arylation
- (2013) Tanguy Saget et al. ORGANIC LETTERS
- Silver-Promoted, Palladium-Catalyzed Direct Arylation of Cyclopropanes: Facile Access to Spiro 3,3′-Cyclopropyl Oxindoles
- (2013) Carolyn L. Ladd et al. ORGANIC LETTERS
- Palladium-Catalyzed Amidation by Chemoselective C(sp3)H Activation: Concise Route to Oxindoles Using a Carbamoyl Chloride Precursor
- (2012) Chihiro Tsukano et al. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
- Palladium(0)-Catalyzed Enantioselective CH Arylation of Cyclopropanes: Efficient Access to Functionalized Tetrahydroquinolines
- (2012) Tanguy Saget et al. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
- Activation of a C(sp3)H Bond by a Transient σ-Alkylpalladium(II) Complex: Synthesis of Spirooxindoles Through a Palladium-Catalyzed Domino Carbopalladation/C(sp3)C(sp3) Bond-Forming Process
- (2012) Tiffany Piou et al. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
- Construction of heterocyclic scaffolds via transition metal-catalyzed sp3 C–H functionalization
- (2012) Ming Zhang et al. JOURNAL OF ORGANOMETALLIC CHEMISTRY
- Ligand-Enabled Methylene C(sp3)–H Bond Activation with a Pd(II) Catalyst
- (2012) Masayuki Wasa et al. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
- Strategies for the enantioselective synthesis of spirooxindoles
- (2012) Nicolas R. Ball-Jones et al. ORGANIC & BIOMOLECULAR CHEMISTRY
- Palladium-Catalyzed Cascade Process Consisting of Isocyanide Insertion and Benzylic C(sp3)–H Activation: Concise Synthesis of Indole Derivatives
- (2012) Takeshi Nanjo et al. ORGANIC LETTERS
- Fused Indolines by Palladium-Catalyzed Asymmetric CC Coupling Involving an Unactivated Methylene Group
- (2011) Masafumi Nakanishi et al. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
- Synergistic Palladium-Catalyzed C(sp3)H Activation/C(sp3)O Bond Formation: A Direct, Step-Economical Route to Benzolactones
- (2011) Petr Novák et al. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
- Palladium-Catalyzed Direct Ethynylation of C(sp3)–H Bonds in Aliphatic Carboxylic Acid Derivatives
- (2011) Yusuke Ano et al. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
- Aerobic Pd-Catalyzed sp3C−H Olefination: A Route to Both N-Heterocyclic Scaffolds and Alkenes
- (2011) Kara J. Stowers et al. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
- Pd(II)-Catalyzed Enantioselective C–H Activation of Cyclopropanes
- (2011) Masayuki Wasa et al. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
- Flexible Strategy for Syntheses of Spirooxindoles using Palladium-Catalyzed Carbosilylation and Sakurai-Type Cyclization
- (2011) Sudhir M. Hande et al. ORGANIC LETTERS
- Palladium(0)-catalyzed cyclopropane C–H bond functionalization: synthesis of quinoline and tetrahydroquinoline derivatives
- (2011) Sophie Rousseaux et al. Chemical Science
- Challenge and progress: palladium-catalyzed sp3 C–H activation
- (2011) Hu Li et al. Catalysis Science & Technology
- Synthesis of Fluorene and Indenofluorene Compounds: Tandem Palladium-Catalyzed Suzuki Cross-Coupling and Cyclization
- (2010) Tao-Ping Liu et al. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
- Palladium-Catalyzed Ligand-Directed C−H Functionalization Reactions
- (2010) Thomas W. Lyons et al. CHEMICAL REVIEWS
- Investigation of the Mechanism of C(sp3)−H Bond Cleavage in Pd(0)-Catalyzed Intramolecular Alkane Arylation Adjacent to Amides and Sulfonamides
- (2010) Sophie Rousseaux et al. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
- Auxiliary-Assisted Palladium-Catalyzed Arylation and Alkylation of sp2and sp3Carbon−Hydrogen Bonds
- (2010) Dmitry Shabashov et al. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
- Palladium-Catalyzed Amidation of Unactivated C(sp3)H Bonds: from Anilines to Indolines
- (2009) Julia J. Neumann et al. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
- Palladium(II)-Catalyzed CH Activation/CC Cross-Coupling Reactions: Versatility and Practicality
- (2009) Xiao Chen et al. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
- Synthesis of Oxindoles by Palladium-catalyzed C–H Bond Amidation
- (2009) Tomoya Miura et al. CHEMISTRY LETTERS
- Asymmetric Syntheses of Oxindole and Indole Spirocyclic Alkaloid Natural Products
- (2009) Barry Trost et al. SYNTHESIS-STUTTGART
- Pd-catalyzed intramolecular amidation of 2-(buta-1,3-dienyl)phenylcarbamoyl chloride: a concise synthesis of spiro[indoline-3,3′-pyrrolidine]
- (2009) Haruhi Kamisaki et al. TETRAHEDRON LETTERS
- Toward General Access to the Aspidosperma-Type Terpenoid Indole Alkaloids: Synthesis of the Key 3,3-Disubstituted Piperidones through Enantioselective Intramolecular Heck-Type Reaction of Chloroformamides
- (2008) Yoshizumi Yasui et al. CHEMICAL & PHARMACEUTICAL BULLETIN
- Synthesis of β-, γ-, and δ-Lactams via Pd(II)-Catalyzed C−H Activation Reactions
- (2008) Masayuki Wasa et al. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
- Palladium-Catalyzed sp3CH Activation of Simple Alkyl Groups: Direct Preparation of Indoline Derivatives fromN-Alkyl-2-bromoanilines
- (2008) Toshiaki Watanabe et al. ORGANIC LETTERS
Create your own webinar
Interested in hosting your own webinar? Check the schedule and propose your idea to the Peeref Content Team.
Create NowAsk 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