About: The Copper-catalyzed Decomposition of Diazoketones1

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scholarly article by Peter Yates published November 1952 in Journal of the American Chemical Society

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в листопаді 1952 (uk) im November 1952 veröffentlichter wissenschaftlicher Artikel (de) scholarly article by Peter Yates published November 1952 in Journal of the American Chemical Society (en)
publication date	wds:Q56815405-2107F4C1-79D9-4B09-8292-0B67F3839834
publication date	1952-11-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q56815405-50B5DB32-A8C8-445E-B66E-D2EF76A9918D
language of work or name	English
author name string	wds:Q56815405-03C2A1A8-9362-4B82-8AE0-F14D5156E8F3
author name string	Peter Yates
rdfs:label	The Copper-catalyzed Decomposition of Diazoketones1 (en) The Copper-catalyzed Decomposition of Diazoketones1 (nl)
skos:prefLabel	The Copper-catalyzed Decomposition of Diazoketones1 (en) The Copper-catalyzed Decomposition of Diazoketones1 (nl)
name	The Copper-catalyzed Decomposition of Diazoketones1 (en) The Copper-catalyzed Decomposition of Diazoketones1 (nl)
title	wds:Q56815405-E1A54CCB-E80A-4C04-8221-A0885913F55C
title	The Copper-catalyzed Decomposition of Diazoketones1 (en)
page(s)	wds:Q56815405-A5503B23-7647-4B3A-B9CA-D28E48A9F6E5
page(s)	5376-5381
instance of	wds:Q56815405-422CF774-6D7A-450C-9EB9-A60C22D834D0
instance of	scholarly article
main subject	wds:Q56815405-BE0A1A4D-CE35-44FF-9CDE-C428BB11A5A4
main subject	copper
published in	wds:Q56815405-B56ABDAC-0D66-4E9D-BBA0-8A3A0E7AD5A2
published in	Journal of the American Chemical Society
issue	wds:Q56815405-A996C097-0500-434E-AF7A-419354F27158
volume	wds:Q56815405-82C562D8-28EF-4F57-8B86-E9AC80D7501D
issue	21
volume	74
DOI	wds:Q56815405-81702BA0-F379-45D4-98AE-34A3C083520B
DOI	http://dx.doi.org/10.1021/JA01141A047
DOI	10.1021/JA01141A047
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q56815405
is cites work of	On the Reaction of Diazoacetyl Compounds with Pepsin Transition metal catalysed reactions of diazocompounds - II insertion in the hydroxylic bond Intermolecular carbene S-H insertion catalysed by engineered myoglobin-based catalysts†. Myoglobin-catalyzed intermolecular carbene N-H insertion with arylamine substrates Cytochrome P450-Catalyzed Insertion of Carbenoids into N-H Bonds Catalytic X-H insertion reactions based on carbenoids Rhodium-Catalysed Enantioselective C-H Functionalization in Asymmetric Synthesis Dimensioning the Term Carbenoid. Catalytic insertion of diazo compounds into N-H bonds: the copper alternative α-Diazocarbonyl Chemistry - Target Driven Applications The inactivation of pepsin by an equimolar amount of 1-diazo-4-phenylbutanone-2 Facts are the enemy of truth-reflections on serendipitous discovery and unforeseen developments in asymmetric catalysis Enantioselective carbenoid insertion into C(sp(3))-H bonds Catalyst-Free Difunctionalization of Activated Alkenes in Water: Efficient Synthesis of β-Keto Sulfides and Sulfones. Stevens rearrangement of thioethers with arynes: a facile access to multi-substituted β-keto thioethers. Chiral dirhodium(II) carboxylates and carboxamidates as effective chemzymes in asymmetric synthesis of three-membered carbocycles Rhodium-carbenoid mediated O-H insertion reactions. O-H insertion vs. H-abstraction and effect of catalyst A Cu-catalyzed four-component cascade reaction to construct β-ester-γ-amino ketones.
is cites work of	wds:Q29391805-A0C03421-D3BC-4A67-9476-EA173ADD066D wds:Q59899117-99BE3B0E-B9FC-4337-8DED-23D8F4E12421 wds:Q60439926-03B9B6E2-E17B-42C4-B4A9-CBC7389E89C2 wds:Q69869775-AA979659-7EF7-4C05-8C46-A13E3CBD70AA wds:Q26747268-05FAB39C-378C-4B60-B6A8-CB60CB28CEB0 wds:Q48123608-AA8010D1-4B18-493B-B5E4-C7D0D3F8E6AA wds:Q38081361-DFE8CCC8-8EFF-48CA-BE91-80906711EEBF wds:Q60408106-15097531-AF9B-4B2F-AC21-30FE46B602AE wds:Q85590593-4B3A264F-AF7B-476D-8316-03F21D37D082 wds:Q38713825-913944C4-61E4-4350-8700-D802A4A3BCBC wds:Q37531521-ABCE3855-1E53-4224-A54D-2FD2C63A5828 wds:Q34808960-2A3EE712-EE57-4A30-97C5-771171F988F5 wds:Q38231755-E24436EB-8F65-4649-AEF0-C616C92A93FF wds:Q51320793-D9F19803-1692-43C4-8907-A95AB7119929 wds:Q35761129-5E7DBC3C-B38B-45ED-B50E-6E96E290BBE3 wds:Q48150850-3C10139D-D01B-4FC3-B617-89A193A49B0A wds:Q71210730-CACB872C-42F9-4A91-B888-8FECA55DC25D wds:Q78821390-F79F99D4-5A66-4EEE-AC9F-FDC4353774C6

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