About: Asymmetric catalysis. 80. Mechanistic aspects of the rhodium-catalyzed enantioselective transfer hydrogenation of .alpha.,.beta.-unsaturated carboxylic acids using formic acid/triethylamine (5:2) as the hydrogen source

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About: Asymmetric catalysis. 80. Mechanistic aspects of the rhodium-catalyzed enantioselective transfer hydrogenation of .alpha.,.beta.-unsaturated carboxylic acids using formic acid/triethylamine (5:2) as the hydrogen source Goto Sponge NotDistinct Permalink

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scholarly article by Walter Leitner et al published January 1993 in Journal of the American Chemical Society

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в січні 1993 (uk) article scientifique publié en 1993 (fr) im Januar 1993 veröffentlichter wissenschaftlicher Artikel (de) scholarly article by Walter Leitner et al published January 1993 in Journal of the American Chemical Society (en)
publication date	wds:Q60244649-1A80F603-2A76-4D82-947E-4692CED97B4F
publication date	1993-01-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q60244649-8B1D7B24-C2B3-46AF-8B60-3665E370F522
language of work or name	English
author name string	wds:Q60244649-227CF03C-D3F4-4D56-A319-83ED51EF52B5 wds:Q60244649-A7D29F35-C0EC-4FCD-AEC1-6A87B9222D01
author name string	John M. Brown Henri Brunner
rdfs:label	Asymmetric catalysis. 80. Mechanistic aspects of the rhodium-catalyzed enantioselective transfer hydrogenation of .alpha.,.beta.-unsaturated carboxylic acids using formic acid/triethylamine (5:2) as the hydrogen source (en) Asymmetric catalysis. 80. Mechanistic aspects of the rhodium-catalyzed enantioselective transfer hydrogenation of .alpha.,.beta.-unsaturated carboxylic acids using formic acid/triethylamine (5:2) as the hydrogen source (nl)
skos:prefLabel	Asymmetric catalysis. 80. Mechanistic aspects of the rhodium-catalyzed enantioselective transfer hydrogenation of .alpha.,.beta.-unsaturated carboxylic acids using formic acid/triethylamine (5:2) as the hydrogen source (en) Asymmetric catalysis. 80. Mechanistic aspects of the rhodium-catalyzed enantioselective transfer hydrogenation of .alpha.,.beta.-unsaturated carboxylic acids using formic acid/triethylamine (5:2) as the hydrogen source (nl)
name	Asymmetric catalysis. 80. Mechanistic aspects of the rhodium-catalyzed enantioselective transfer hydrogenation of .alpha.,.beta.-unsaturated carboxylic acids using formic acid/triethylamine (5:2) as the hydrogen source (en) Asymmetric catalysis. 80. Mechanistic aspects of the rhodium-catalyzed enantioselective transfer hydrogenation of .alpha.,.beta.-unsaturated carboxylic acids using formic acid/triethylamine (5:2) as the hydrogen source (nl)
author	wds:Q60244649-27CD9757-D0F6-48F7-8866-F481D74C2BFA
author	Walter Leitner
title	wds:Q60244649-13E55318-C3E7-4AFE-A580-CCCA23267BE7
title	Asymmetric catalysis. 80. Mechanistic aspects of the rhodium-catalyzed enantioselective transfer hydrogenation of .alpha.,.beta.-unsaturated carboxylic acids using formic acid/triethylamine (5:2) as the hydrogen source (en)
page(s)	wds:Q60244649-69411909-53ED-4A5A-BE81-719C50886AB6
page(s)	152-159
instance of	wds:Q60244649-616D39DC-B165-4C83-9C16-4D90E0CACCC1
instance of	scholarly article
main subject	wds:Q60244649-B98FE07E-37C1-4A6A-8B26-423331C91D1F wds:Q60244649-BB5CCF42-D151-44C5-8D55-1B13DCCD6B77
main subject	rhodium enantioselectivity
published in	wds:Q60244649-42B7ECCD-5256-4E06-9442-9493ECEC53D1
published in	Journal of the American Chemical Society
issue	wds:Q60244649-A35C7BE7-E1F2-4A54-B29F-6C9E78142EE0
volume	wds:Q60244649-E46B9086-06A1-4DF0-BED2-2AF9CAE65C95
issue	1
volume	115
number of pages	wds:Q60244649-B1993799-A6AF-40A9-AC45-8313DA7616F6
number of pages	8 (xsd:decimal)
DOI	wds:Q60244649-9100DE31-C6E6-4E17-A11C-132FD8472413
DOI	http://dx.doi.org/10.1021/JA00054A021
DOI	10.1021/JA00054A021
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q60244649
is cites work of	Mechanistic aspects of dihydrogen activation and transfer during asymmetric hydrogenation in supercritical carbon dioxide Transfer Hydrogenation of Ketones and Activated Olefins Using Chelating NHC Ruthenium Complexes Asymmetric synthesis of γ-branched amines via rhodium-catalyzed reductive amination. ‘Diopium’, a chiral phosphoniophosphine derived from Kagan's diop. Rhodium complexes and reducing catalytic properties
is cites work of	wds:Q60244583-26BDFF5A-B201-441A-8714-38F871549D1F wds:Q51736352-23C92160-7AF9-48F8-989E-DF9E5181E834 wds:Q59359267-86E71CC0-B215-4C04-8086-CD4E6074BD03 wds:Q57502985-B34B1707-D64A-4DD0-A578-3C7A2C6D8B12

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