About: Cobalt-catalyzed asymmetric cyclopropanation of electron-deficient olefins

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About: Cobalt-catalyzed asymmetric cyclopropanation of electron-deficient olefins Goto Sponge NotDistinct Permalink

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scientific article published on 18 September 2007

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована у вересні 2007 (uk) scientific article published on 18 September 2007 (en) artículu científicu espublizáu en setiembre de 2007 (ast)
publication date	wds:Q81314242-913A83AB-8734-4D26-8D0E-B70BEF9EE5D4
publication date	2007-09-18 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q81314242-605C1728-BAB1-4438-88CB-A218193D0F31
language of work or name	English
cites work	wds:Q81314242-2B12D7DB-BB68-4E86-9E8F-950CA6082866
cites work	Bis(oxazolines) as chiral ligands in metal-catalyzed asymmetric reactions. Catalytic, asymmetric cyclopropanation of olefins
author name string	wds:Q81314242-60A18FBD-72D8-4473-A337-D3A119475B30 wds:Q81314242-72C6BD8B-8464-47D3-91AE-7024F3682999
author name string	Ying Chen Joshua V Ruppel
rdfs:label	Cobalt-catalyzed asymmetric cyclopropanation of electron-deficient olefins (en) Cobalt-catalyzed asymmetric cyclopropanation of electron-deficient olefins (nl)
skos:prefLabel	Cobalt-catalyzed asymmetric cyclopropanation of electron-deficient olefins (en) Cobalt-catalyzed asymmetric cyclopropanation of electron-deficient olefins (nl)
name	Cobalt-catalyzed asymmetric cyclopropanation of electron-deficient olefins (en) Cobalt-catalyzed asymmetric cyclopropanation of electron-deficient olefins (nl)
author	wds:Q81314242-2F47E69F-4653-411E-9288-233280554936
author	Peter Zhang
title	wds:Q81314242-B4FE3DD0-1C1B-4123-B814-BAD94F2603AA
title	Cobalt-catalyzed asymmetric cyclopropanation of electron-deficient olefins (en)
page(s)	wds:Q81314242-A8A90FBA-70F7-46D1-8C0C-57D94308B4D8
page(s)	12074-12075
instance of	wds:Q81314242-00895A66-9136-4A43-ABEC-951555F87BA7
instance of	scholarly article
main subject	wds:Q81314242-0C9A1407-CE59-41D4-9EE0-3DBFD5B11A29 wds:Q81314242-5C622D7A-6CAA-485A-A5ED-E25597CDD469
main subject	cobalt cyclopropanation
PubMed ID	wds:Q81314242-76F1251D-B30D-4588-817D-2B9A44F32264
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/17877352
PubMed ID	17877352
published in	wds:Q81314242-57E0FC49-6EE8-455F-B632-DDAC094444F9
published in	Journal of the American Chemical Society
issue	wds:Q81314242-30C14DCA-E677-49B0-9959-8CB0B860D8C0
volume	wds:Q81314242-AF99207A-27C7-44FC-B4B7-248E4D05B5CE
issue	40
volume	129
DOI	wds:Q81314242-DE0953D4-BD59-4EE4-ACB8-A580A7A6DD36
DOI	http://dx.doi.org/10.1021/JA074613O
DOI	10.1021/JA074613O
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q81314242
is cites work of	Synthesis, pharmacological characterization, and structure-activity relationship studies of small molecular agonists for the orphan GPR88 receptor. Stereoselective Radical C-H Alkylation with Acceptor/Acceptor-Substituted Diazo Reagents via Co(II)-Based Metalloradical Catalysis Characterization of Tunable Radical Metal-Carbenes: Key Intermediates in Catalytic Cyclopropanation. Cobalt(II)-catalyzed asymmetric olefin cyclopropanation with α-ketodiazoacetates Asymmetric Radical Cyclopropanation of Alkenes with In Situ-Generated Donor-Substituted Diazo Reagents via Co(II)-Based Metalloradical Catalysis Regioselective synthesis of multisubstituted furans via metalloradical cyclization of alkynes with α-diazocarbonyls: construction of functionalized α-oligofurans. Diastereoselective Radical-Type Cyclopropanation of Electron-Deficient Alkenes Mediated by the Highly Active Cobalt(II) Tetramethyltetraaza[14]annulene Catalyst Metalloradical approach to 2H-chromenes. Characterization of Porphyrin-Co(III)-'Nitrene Radical' Species Relevant in Catalytic Nitrene Transfer Reactions Exceptional selectivity in cyclopropanation reactions catalyzed by chiral cobalt(II)-porphyrin catalysts Porphyrin Cobalt(III) "Nitrene Radical" Reactivity; Hydrogen Atom Transfer from Ortho-YH Substituents to the Nitrene Moiety of Cobalt-Bound Aryl Nitrene Intermediates (Y = O, NH). Catalytic and Biocatalytic Iron Porphyrin Carbene Formation: Effects of Binding Mode, Carbene Substituent, Porphyrin Substituent, and Protein Axial Ligand. Metalloradical activation of α-formyldiazoacetates for the catalytic asymmetric radical cyclopropanation of alkenes. Catalytic Radical Process for Enantioselective Amination of C(sp3)-H Bonds Rhodium-catalyzed enantioselective cyclopropanation of electron deficient alkenes. Diverse Engineered Heme Proteins Enable Stereodivergent Cyclopropanation of Unactivated Alkenes. Stereodivergent Rhodium(III)-Catalyzed cis-Cyclopropanation Enabled by Multivariate Optimization Cyclopropanation Reactions Mediated by Group 9 Metal Porphyrin Complexes Carbene radicals in cobalt(II)-porphyrin-catalysed carbene carbonylation reactions; a catalytic approach to ketenes Stereoselective Intramolecular Cyclopropanation of α-Diazoacetates via Co(II)-Based Metalloradical Catalysis. Chiral cyclopentadienyl Rh-catalyzed enantioselective cyclopropanation of electron-deficient olefins enable rapid access to UPF-648 and oxylipin natural products Cyclopropanations via Heme Carbenes: Basic Mechanism and Effects of Carbene Substituent, Protein Axial Ligand, and Porphyrin Substitution. Metal-Diazo Radicals of α-Carbonyl Diazomethanes [Co(MeTAA)] Metalloradical Catalytic Route to Ketenes via Carbonylation of Carbene Radicals Rh(III)-Catalyzed C-H Activation-Initiated Directed Cyclopropanation of Allylic Alcohols
is cites work of	wds:Q57800789-46F21DA9-DB5C-48E1-8BFA-7660642855AE wds:Q35153979-950E8EDA-9231-4BD0-8A3C-EECAEC6F013A wds:Q36570787-290C993E-D5CD-4771-8536-B3A7906F7D6D wds:Q64266919-9ACE6C7B-A80C-4971-8665-1DD524FF5ECF wds:Q36670936-EA995FF9-2096-4C9C-A6D9-53C29147F802 wds:Q46591390-E7E3DCEB-1D14-4908-9ED8-3F12958B011F wds:Q37605771-98ADEAFD-526C-41F0-A57B-7598DBFC77FF wds:Q34315051-BCD06D66-8680-4A92-A218-2D82DF6194E6 wds:Q34548536-96C83D38-C53A-4CD3-8C70-E2E0F7DB2FDB wds:Q56740053-BF3184AE-9231-46E6-BEF5-24BB78FADA0B wds:Q33705747-08E6821F-E4F4-4D11-A8F0-08910C2917AA wds:Q42271761-4A1ADA81-5E34-4D73-9EFF-1131FE5670BD wds:Q52597441-57B1607A-A484-4035-95E7-08160411C052 wds:Q35787250-6B8F523F-B110-4ACE-9224-432582787C80 wds:Q43142935-14A3A4E6-DB0C-485E-AE4F-C90607D7D9A1 wds:Q90396639-F8330E23-7DCD-48EF-BED8-7A5D2794AB62 wds:Q34190065-76900937-6592-449C-95A5-A80D6C88548A wds:Q34912950-211C0189-9498-4636-AA2E-69A58498D0AC wds:Q34376980-ADF13127-79C1-49ED-9C33-E072C7EC79E8 wds:Q41671212-8AA890D7-891D-47F6-BC99-1B637E96F80B wds:Q47264065-11BA14EF-CF21-4900-9E27-CDA38335CB16 wds:Q93175240-376C6220-1439-46E9-AFD9-74ABEA3037B4 wds:Q33918230-400BCB7E-F3D3-45FA-8BBA-E9D26774A9ED wds:Q37172196-A5DD511E-2D47-403E-83F1-8F9636EB1D8B wds:Q59079382-EC0E7038-09F8-4681-A539-B4A95E6FD310

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