About: Silver-catalyzed carboxylation

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scientific article (publication date: 2016)

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rdf:type	Item
description	artikull shkencor (sq) wetenschappelijk artikel (nl) artículu científicu espublizáu en 2016 (ast) مقالة علمية (نشرت عام 2016) (ar) 2016 թվականին հրատարակված գիտական հոդված (hy) наукова стаття, опублікована у 2016 (uk) 2016 թուականին հրատարակուած գիտական յօդուած (hyw) scientific article (publication date: 2016) (en) im Januar 2016 veröffentlichter wissenschaftlicher Artikel (de)
publication date	wds:Q29012481-4DE357A9-286A-4849-A2DD-5DCB902406D5
publication date	2016-08-01 00:00:00Z (xsd:dateTime)
author name string	wds:Q29012481-2D3C5E7F-CAEC-4B19-A452-D978A92107C6
author name string	T Yamada
rdfs:label	Silver-catalyzed carboxylation (en) Silver-catalyzed carboxylation (ast)
skos:prefLabel	Silver-catalyzed carboxylation (en) Silver-catalyzed carboxylation (ast)
name	Silver-catalyzed carboxylation (en) Silver-catalyzed carboxylation (ast)
author	wds:Q29012481-53CDBBAD-59AE-4F15-B3AB-0E5C528280BB
author	Kohei Sekine
title	wds:Q29012481-B509CA34-11A3-4700-B4F1-692E620F7828
title	Silver-catalyzed carboxylation (en)
page(s)	wds:Q29012481-15C99939-DFFA-4BCF-A3CE-5C22F3F3AC9C
page(s)	4524-4532
instance of	wds:Q29012481-B93B2402-338A-4922-BED1-49CD3DC9231B
instance of	scholarly article
PubMed ID	wds:Q29012481-EFECE46A-C3E1-4BB1-903F-118676321022
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/26888406
PubMed ID	26888406
published in	wds:Q29012481-7DF94BF9-62BA-4400-8854-9E6C01379D20
published in	Chemical Society Reviews
issue	wds:Q29012481-D2A6C2A6-34DB-4B92-BE42-D3E7517F9C9D
volume	wds:Q29012481-F76E92EA-EBF9-40E9-A7E0-636C2152C5BE
issue	16
volume	45
DOI	wds:Q29012481-74EF32E3-D236-4F8C-89F7-132117D1BB9D
DOI	http://dx.doi.org/10.1039/C5CS00895F
DOI	10.1039/C5CS00895F
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q29012481
is cites work of	An ultrastable zirconium-phosphonate framework as bifunctional catalyst for highly active CO2 chemical transformation. Cs2CO3 as a source of carbonyl and ethereal oxygen in a Cu-catalysed cascade synthesis of benzofuran [3,2-c] quinolin-6[5-H]ones. Ni- and Fe-catalyzed Carboxylation of Unsaturated Hydrocarbons with CO2. AgI /TMG-Promoted Cascade Reaction of Propargyl Alcohols, Carbon Dioxide, and 2-Aminoethanols to 2-Oxazolidinones. Silver(I)-Promoted Cascade Reaction of Propargylic Alcohols, Carbon Dioxide, and Vicinal Diols: Thermodynamically Favorable Route to Cyclic Carbonates One-pot carboxylative cyclization of propargylic alcohols and CO2 catalysed by N -heterocyclic carbene/Ag systems Carboxylation Reactions Using Carbon Dioxide as the C1 Source via Catalytically Generated Allyl Metal Intermediates Triphenylphosphine-based functional porous polymer as an efficient heterogeneous catalyst for the synthesis of cyclic carbonates from CO2. Stereospecific Decarboxylative Nazarov Cyclization Mediated by Carbon Dioxide for the Preparation of Highly Substituted 2-Cyclopentenones. Chemical reduction of CO2 facilitated by C-nucleophiles. Toward ideal carbon dioxide functionalization A Core-Shell-Structured Silver Nanowire/Nitrogen-Doped Carbon Catalyst for Enhanced and Multifunctional Electrofixation of CO2 Metal-Free Photocatalytic Synthesis of exo-Iodomethylene 2-Oxazolidinones: An Alternative Strategy for CO2 Valorization with Solar Energy Silver-Catalyzed Oxidative C(sp3 )-P Bond Formation through C-C and P-H Bond Cleavage. Cobalt- and rhodium-catalyzed carboxylation using carbon dioxide as the C1 source An Experimental and Theoretical Study on the Unexpected Catalytic Activity of Triethanolamine for the Carboxylative Cyclization of Propargylic Amines with CO2. A simple and robust AgI/KOAc catalytic system for the carboxylative assembly of propargyl alcohols and carbon dioxide at atmospheric pressure Silver(I)-Catalyzed Intramolecular Cyclizations of Epoxide-Propargylic Esters to 1,4-Oxazine Derivatives Catalytic, Enantioselective Synthesis of Cyclic Carbamates from Dialkyl Amines by CO2-Capture: Discovery, Development, and Mechanism Across the Board: Arjan W. Kleij on Electrosynthesis for Regioselective Carboxylation of Aromatic Alkenes
is cites work of	wds:Q54269631-A44B191A-EC36-47EA-B439-0E539FDCE62A wds:Q48205292-8DDA56E5-B4E1-494E-AAFC-D7FC8CC41674 wds:Q57820334-69E71A2F-8C1A-4E94-BA1D-7C4709FA9A15 wds:Q91975535-97EF641A-3A9B-4A39-B78C-3C0D8D350712 wds:Q48094964-6009C1C3-EA43-4DFD-97D1-A1A8C21F61D6 wds:Q48642716-FED2E774-2E41-437F-BFE7-CE96D762907F wds:Q64227986-BFB78C86-813D-4B32-B2B4-C2A61646839E wds:Q91003698-9533D844-02B1-4F51-898A-40F71206E0FD wds:Q92925754-11E42D6C-2C9B-4861-A977-7A5C0A927471 wds:Q38940349-6AC09607-990A-419C-BCD1-0532873A7ED1 wds:Q47981886-50684E3D-ED7D-45F5-89D8-D09C6F8805AA wds:Q57821996-837F4A4C-2EF5-4B70-B888-3B2ED021589A wds:Q33469968-B89A6FC4-E425-4159-AC57-8C526BA8D191 wds:Q47096215-5269FD03-A86C-4FDF-8B24-535E51E42A76 wds:Q48373782-38A76725-E0C6-4CC1-9B54-6F043662328E wds:Q57820434-5E79741C-73DC-4706-B552-EC409C89E048 wds:Q37620608-06CE0719-8FBB-4704-BDA0-4909D09D6BBF wds:Q91035638-E8378A37-7454-49C4-8841-0F4CEF36ED21 wds:Q90734787-9487BA2F-69F7-4FDF-B768-0E5416336F41 wds:Q90102750-C84A75EA-510F-4163-ACED-868F9EABB7AA

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