Literature DB >> 17994656

A supramolecular catalyst for regioselective hydroformylation of unsaturated carboxylic acids.

Tomás Smejkal1, Bernhard Breit.   

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Year:  2008        PMID： 17994656     DOI： 10.1002/anie.200703192

Source DB:  PubMed          Journal:  Angew Chem Int Ed Engl        ISSN： 1433-7851            Impact factor:   15.336


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  17 in total

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3.  Enantioselective hydroformylation of aniline derivatives.

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4.  Ir-Catalyzed ortho-Borylation of Phenols Directed by Substrate-Ligand Electrostatic Interactions: A Combined Experimental/in Silico Strategy for Optimizing Weak Interactions.

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Review 5.  Transition Metal Catalysis Controlled by Hydrogen Bonding in the Second Coordination Sphere.

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6.  A robust polyfunctional Pd(II)-based magnetic amphiphilic nanocatalyst for the Suzuki-Miyaura coupling reaction.

Authors:  Hamideh Aghahosseini; Mohammad Reza Saadati; Seyed Jamal Tabatabaei Rezaei; Ali Ramazani; Narges Asadi; Hidenori Yahiro; Masami Mori; Nahid Shajari; Ali Reza Kazemizadeh
Journal:  Sci Rep       Date:  2021-05-13       Impact factor: 4.379

7.  Distal-selective hydroformylation using scaffolding catalysis.

Authors:  Candice L Joe; Thomas P Blaisdell; Allison F Geoghan; Kian L Tan
Journal:  J Am Chem Soc       Date:  2014-06-06       Impact factor: 15.419

8.  meta-Selective C-H Borylation of Benzylamine-, Phenethylamine-, and Phenylpropylamine-Derived Amides Enabled by a Single Anionic Ligand.

Authors:  Holly J Davis; Georgi R Genov; Robert J Phipps
Journal:  Angew Chem Int Ed Engl       Date:  2017-09-19       Impact factor: 15.336

9.  Harnessing non-covalent interactions to exert control over regioselectivity and site-selectivity in catalytic reactions.

Authors:  Holly J Davis; Robert J Phipps
Journal:  Chem Sci       Date:  2016-10-05       Impact factor: 9.825

Review 10.  Supramolecular Approaches To Control Activity and Selectivity in Hydroformylation Catalysis.

Authors:  Sandra S Nurttila; Pim R Linnebank; Tetiana Krachko; Joost N H Reek
Journal:  ACS Catal       Date:  2018-03-09       Impact factor: 13.084
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