An Efficient Protocol for the Synthesis of Primary Amides via Rh-Catalyzed Rearrangement of Aldoximes
Published 2018 View Full Article
- Home
- Publications
- Publication Search
- Publication Details
Title
An Efficient Protocol for the Synthesis of Primary Amides via Rh-Catalyzed Rearrangement of Aldoximes
Authors
Keywords
-
Journal
ChemistrySelect
Volume 3, Issue 12, Pages 3474-3478
Publisher
Wiley
Online
2018-04-06
DOI
10.1002/slct.201800265
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- Water-tolerant bis(allyl)-ruthenium(IV) catalysts: An account of their applications
- (2017) Javier Francos et al. INORGANICA CHIMICA ACTA
- Nabscessins A and B, Aminocyclitol Derivatives from Nocardia abscessus IFM 10029T
- (2017) Shoko Hara et al. JOURNAL OF NATURAL PRODUCTS
- A selective hydration of nitriles catalysed by a Pd(OAc) 2 -based system in water
- (2017) Daniel D. Sanz Sharley et al. TETRAHEDRON LETTERS
- Amidation of carboxylic acids via the mixed carbonic carboxylic anhydrides and its application to synthesis of antidepressant (1 S ,2 R )-tranylcypromine
- (2017) Tetsuya Ezawa et al. TETRAHEDRON-ASYMMETRY
- External or internal surface of H-ZSM-5 zeolite, which is more effective for the Beckmann rearrangement reaction?
- (2017) Yueying Chu et al. Catalysis Science & Technology
- Copper-catalyzed one-pot oxidative amidation between methylarenes and amines
- (2017) Yuhang Yang et al. RSC Advances
- Ru-Ferrite-Decorated Graphene (RuFG): A Sustainable and Efficient Catalyst for Conversion of Aromatic Aldehydes and Nitriles to Primary Amides in Aqueous Medium
- (2017) Ramen Jamatia et al. ACS Sustainable Chemistry & Engineering
- Aminofluorene-Mediated Biomimetic Domino Amination–Oxygenation of Aldehydes to Amides
- (2016) Santanu Ghosh et al. ORGANIC LETTERS
- Highly efficient synthesis of primary amides via aldoximes rearrangement in water under air atmosphere catalyzed by an ionic ruthenium pincer complex
- (2016) Fa-Liu Yang et al. RSC Advances
- Palladium nanoparticles immobilized on an amine-functionalized MIL-101(Cr) as a highly active catalyst for oxidative amination of aldehydes
- (2016) Mrinal Saikia et al. RSC Advances
- Catalytic synthesis of amides via aldoximes rearrangement
- (2015) Pascale Crochet et al. CHEMICAL COMMUNICATIONS
- An efficient ruthenium(iv) catalyst for the selective hydration of nitriles to amides in water under mild conditions
- (2014) Eder Tomás-Mendivil et al. CHEMICAL COMMUNICATIONS
- Nanoparticle catalysts for nitrile hydration
- (2014) Emma L. Downs et al. COORDINATION CHEMISTRY REVIEWS
- Metal-catalyzed nitrile hydration reactions: The specific contribution of ruthenium
- (2014) Rocío García-Álvarez et al. JOURNAL OF ORGANOMETALLIC CHEMISTRY
- Tandem Synthesis of N-Alkylated Amides from Aldoximes and Alcohols by Using a Ru/Ir Dual-Catalyst System
- (2013) Feng Li et al. ChemCatChem
- Safety Profile of Modafinil Across a Range of Prescribing Indications, Including Off-Label Use, in a Primary Care Setting in England
- (2013) Miranda Davies et al. DRUG SAFETY
- A general and practical oxidation of alcohols to primary amides under metal-free conditions
- (2013) Xiao-Feng Wu et al. GREEN CHEMISTRY
- Thiazolyl-phosphine hydrochloride salts: effective auxiliary ligands for ruthenium-catalyzed nitrile hydration reactions and related amide bond forming processes in water
- (2013) Rocío García-Álvarez et al. GREEN CHEMISTRY
- Iron-catalysed oxidative amidation of alcohols with amines
- (2013) Silvia Gaspa et al. ORGANIC & BIOMOLECULAR CHEMISTRY
- Rearrangement of aldoximes to amides in water under air atmosphere catalyzed by water-soluble iridium complex [Cp*Ir(H2O)3][OTf]2
- (2013) Chunlou Sun et al. Catalysis Science & Technology
- Efficient and practical transition metal-free catalytic hydration of organonitriles to amides
- (2012) Tao Tu et al. GREEN CHEMISTRY
- Palladium(II) Containing γ-Keggin Silicodecatungstate That Efficiently Catalyzes Hydration of Nitriles
- (2012) Tomohisa Hirano et al. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
- An efficient copper(II)-catalyzed direct access to primary amides from aldehydes under neat conditions
- (2012) Nemai C. Ganguly et al. TETRAHEDRON LETTERS
- An alternate synthesis of enantiomerically pure levetiracetam (Keppra®)
- (2012) M. Mujahid et al. TETRAHEDRON-ASYMMETRY
- Direct amide formation from unactivated carboxylic acids and amines
- (2011) C. Liana Allen et al. CHEMICAL COMMUNICATIONS
- Metal-catalysed approaches to amide bond formation
- (2011) C. Liana Allen et al. CHEMICAL SOCIETY REVIEWS
- Efficient and Substrate-Specific Hydration of Nitriles to Amides in Water by Using a CeO2 Catalyst
- (2011) Masazumi Tamura et al. CHEMISTRY-A EUROPEAN JOURNAL
- Rethinking amide bond synthesis
- (2011) Vijaya R. Pattabiraman et al. NATURE
- Copper-catalyzed rearrangement of oximes into primary amides
- (2011) Sumeet K. Sharma et al. TETRAHEDRON LETTERS
- Copper(II)-catalyzed hydration of nitriles with the aid of acetaldoxime
- (2011) Xiao-Yun Ma et al. TETRAHEDRON LETTERS
- Bis(allyl)ruthenium(IV) Complexes Containing Water-Soluble Phosphane Ligands: Synthesis, Structure, and Application as Catalysts in the Selective Hydration of Organonitriles into Amides
- (2010) Victorio Cadierno et al. CHEMISTRY-A EUROPEAN JOURNAL
- Efficient Iodine-Mediated Beckmann Rearrangement of Ketoximes to Amides under Mild Neutral Conditions
- (2010) Nemai Ganguly et al. SYNTHESIS-STUTTGART
- Cost efficient synthesis of amides from oximes with indium or zinc catalysts
- (2010) C. Liana Allen et al. TETRAHEDRON LETTERS
- Significant Self-Acceleration Effects of Nitrile Additives in the Rhodium-Catalyzed Conversion of Aldoximes to Amides: A New Mechanistic Aspect
- (2009) Min Kim et al. ADVANCED SYNTHESIS & CATALYSIS
- Amide bond formation: beyond the myth of coupling reagents
- (2008) Eric Valeur et al. CHEMICAL SOCIETY REVIEWS
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