About: C2-Symmetric 4,4′,5,5′-Tetrahydrobi(oxazoles) and 4,4′,5,5′-Tetrahydro-2,2′-methylenebis[oxazoles] as Chiral Ligands for Enantioselective Catalysis Preliminary Communication

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About: C2-Symmetric 4,4′,5,5′-Tetrahydrobi(oxazoles) and 4,4′,5,5′-Tetrahydro-2,2′-methylenebis[oxazoles] as Chiral Ligands for Enantioselective Catalysis Preliminary Communication Goto Sponge NotDistinct Permalink

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rdf:type	Item
description	article (en) ലേഖനം (ml) wetenschappelijk artikel (nl) наукова стаття, опублікована в січні 1991 (uk) article scientifique publié en 1991 (fr) im Januar 1991 veröffentlichter wissenschaftlicher Artikel (de)
publication date	wds:Q56517258-5C94EC90-2DE8-415F-811E-48AE72D9C194
publication date	1991-01-30 00:00:00Z (xsd:dateTime)
cites work	wds:Q56517258-4F2BC692-5C0E-4F5D-9D73-09ACDB125943 wds:Q56517258-8E0C9022-A41C-42EF-853D-135E5EE74FAC wds:Q56517258-91CCD697-39E8-469E-A792-1F9E23A84179 wds:Q56517258-C44EC688-E5BD-4354-B836-8B8227CFACBF wds:Q56517258-F3933F72-EB38-4089-A0E0-F13D0BB5E22C
cites work	Asymmetric catalytic cyclopropanation of olefins: bis-oxazoline copper complexes A new system for catalytic enantioselective reduction of achiral ketones to chiral alcohols. Synthesis of chiral α-hydroxy acids Gaschromatographische Enantiomerentrennung an Cyclodextrinderivaten Chiral Copper-Semicorrin Complexes as Enantioselective Catalysts for the Cyclopropanation of Olefins by Diazo Compounds Highly enantioselective borane reduction of ketones catalyzed by chiral oxazaborolidines. Mechanism and synthetic implications
author name string	wds:Q56517258-2FA2A2D8-29BA-4191-B849-30C330FBAC41 wds:Q56517258-CCD4D1E7-185A-4ACD-8D23-C297896A0412 wds:Q56517258-D85DDDF3-512B-4EE9-8362-88DEAA0C6CB3 wds:Q56517258-F8543036-EE0F-4701-BDF2-84762DE48472
author name string	Dieter Müller Andreas Pfaltz Beat Weber Gisela Umbricht
rdfs:label	C2-Symmetric 4,4′,5,5′-Tetrahydrobi(oxazoles) and 4,4′,5,5′-Tetrahydro-2,2′-methylenebis[oxazoles] as Chiral Ligands for Enantioselective Catalysis Preliminary Communication (en) C2-Symmetric 4,4′,5,5′-Tetrahydrobi(oxazoles) and 4,4′,5,5′-Tetrahydro-2,2′-methylenebis[oxazoles] as Chiral Ligands for Enantioselective Catalysis Preliminary Communication (nl)
skos:prefLabel	C2-Symmetric 4,4′,5,5′-Tetrahydrobi(oxazoles) and 4,4′,5,5′-Tetrahydro-2,2′-methylenebis[oxazoles] as Chiral Ligands for Enantioselective Catalysis Preliminary Communication (en) C2-Symmetric 4,4′,5,5′-Tetrahydrobi(oxazoles) and 4,4′,5,5′-Tetrahydro-2,2′-methylenebis[oxazoles] as Chiral Ligands for Enantioselective Catalysis Preliminary Communication (nl)
name	C2-Symmetric 4,4′,5,5′-Tetrahydrobi(oxazoles) and 4,4′,5,5′-Tetrahydro-2,2′-methylenebis[oxazoles] as Chiral Ligands for Enantioselective Catalysis Preliminary Communication (en) C2-Symmetric 4,4′,5,5′-Tetrahydrobi(oxazoles) and 4,4′,5,5′-Tetrahydro-2,2′-methylenebis[oxazoles] as Chiral Ligands for Enantioselective Catalysis Preliminary Communication (nl)
title	wds:Q56517258-4338670F-5AF6-4506-91BD-A6E79AE8BE38
title	C2-Symmetric 4,4′,5,5′-Tetrahydrobi(oxazoles) and 4,4′,5,5′-Tetrahydro-2,2′-methylenebis[oxazoles] as Chiral Ligands for Enantioselective Catalysis Preliminary Communication (en)
page(s)	wds:Q56517258-C8950233-EC9C-44A0-961E-E68F76DABB4B
page(s)	232-240
instance of	wds:Q56517258-26338370-5B8A-464F-B550-FAC7192DF211
instance of	scholarly article
main subject	wds:Q56517258-1B69EDFB-8915-4030-B8FD-376DBE545B5E wds:Q56517258-41B78AFE-0D3C-4EF4-AD6F-239F8CB0F73C wds:Q56517258-6F80CE44-AAD9-42B7-86DC-698B111940C3 wds:Q56517258-EC9A97B4-E249-410C-B87A-DDB2301161D4
main subject	drug discovery catalysis chirality enantioselectivity
published in	wds:Q56517258-6D303899-E866-4C1C-B7A8-6EFDB60F2E77
published in	Helvetica Chimica Acta
issue	wds:Q56517258-6C5C3100-01D4-4EC2-A23B-F1BE8E6D5CC1
volume	wds:Q56517258-FEC2EF27-0A7B-40B0-A684-DB9563BBC934
issue	1
volume	74
DOI	wds:Q56517258-7B0D1AAB-2F92-4F67-8C5A-F33BF656C6F9
DOI	http://dx.doi.org/10.1002/HLCA.19910740123
DOI	10.1002/HLCA.19910740123
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q56517258
is cites work of	Broader, greener, and more efficient: recent advances in asymmetric transfer hydrogenation. Asymmetric Catalysis by Architectural and Functional Molecular Engineering: Practical Chemo- and Stereoselective Hydrogenation of Ketones Design of chiral ligands for asymmetric catalysis: from C2-symmetric P,P- and N,N-ligands to sterically and electronically nonsymmetrical P,N-ligands Bisoxazolines with one and two sidearms: stereodirecting ligands for copper-catalysed asymmetric allylic oxidations of alkenes C 2-Symmetric chiral bis(oxazoline)-metal complexes in catalytic asymmetric synthesis Preparation and Catalytic Enantioselective Reactions ofC3-Symmetric Tris(Oxazoline)s Derived from Kemp's Triacid Coordination chemistry of oxazoline ligands Immobilisation of bis(oxazoline)–copper complexes on clays and nanocomposites. Influence of different parameters on activity and selectivity Enantioselective Borohydride Reduction Catalyzed by Optically Active Cobalt Complexes On the mechanism of the copper-catalyzed cyclopropanation reaction A new C2-symmetric chiral bisphosphine ligand containing a bioxazole backbone: highly enantioselective hydrosilylation of ketones Synthesis of new C2-symmetric bioxazoles and application as chiral ligands in asymmetric hydrosilylation Phosphine-pyridyl and related ligands in synthesis and catalysis Copper complexes with multidentate ligands derived from l-proline. X-ray crystal structure of {[Cu(N,N′-bis[(S)-prolyl]ethylenediamine)]ClO4}2·(MeCN)2 A Novel Methodology for the Synthesis of Cyclic Carbonates Based on the Palladium-Catalyzed Cascade Reaction of 4-Methoxycarbonyloxy-2-butyn-1-ols with Phenols, Involving a Novel Carbon Dioxide Elimination-Fixation Process New chiral 2,2′:6′,2″-terpyridine ligands from the chiral pool: synthesis, crystal structure of a rhodium complex and uses in copper- and rhodium-catalyzed enantioselective cyclopropanation of styrene Syntheses and Crystal Structures of 4,5-Dihydro-2-(2?-hydroxyphenyl)oxazole-Containing Metal Complexes Preparation of enantiopure biimidazoline ligands and their use in asymmetric catalysis New benzotriazole derivatives as multifunctional ligands Homochiral coordination cages assembled from dinuclear paddlewheel nodes and enantiopure ditopic ligands: syntheses, structures and catalysis. Enantioselective mukaiyama-michael reactions of 2-carbomethoxy cyclopentenone catalyzed by chiral bis(Oxazoline)-Cu(II) complexes Asymmetric catalysis with chiral oxazolidine ligands Effect of the molar ratio of an energy source to the substrate on yeast-mediated production of 2-chloro-alpha-methylbenzyl alcohol. Synthesis with a strong hand 1,1'-Bis(oxazolin-2-yl)ferrocenes: An Investigation of Their Complexation Behavior toward [Pd(?3-allyl)Cl]2 Copper and manganese complexes with C2-multitopic ligands. X-ray crystal structure of [Cu(N,N′-bis[(S)-prolyl]phenylenediamine)H2O]. Catalytic properties Catalytic reduction of acetophenone with transition metal systems containing chiral bis(oxazolines)
is cites work of	wds:Q29541244-F8F9909E-EEA2-41B7-8F16-41535A04E530 wds:Q58214376-57692238-4BCB-48FE-B73B-D9AC7DFA3E86 wds:Q46853793-F696A201-62DA-4D48-ABBD-7640029A9FCD wds:Q61946018-FB0C6B78-A160-4D05-B57D-FFC68F832388 wds:Q60215937-29A1F4F7-8735-40E3-9162-5E95736004D2 wds:Q44404362-DFB4D0FB-6266-4649-8EE6-5497943EAFEA wds:Q44591923-595C2208-97AB-4F5A-86C1-16CD8FBC6FE2 wds:Q61884046-AC34174D-7FC8-4ECF-A832-BC1F34F9E96D wds:Q63345188-CDB44C83-D822-49B6-B935-2C10AF2FDF1D wds:Q53300372-15236AFE-A0AD-4D91-920F-2ECAE80498C4 wds:Q93237621-DA961952-BA6D-4AF2-B00B-982CF52E7F78 wds:Q53653020-3C669126-1BC4-421A-A765-4398E7D94CEB wds:Q77581860-AE35E1CA-DA1C-4BFC-8CA1-F70734CF9779 wds:Q37829921-BBF30AC7-908D-4DA4-B6C9-E0EF26DC4666 wds:Q60240483-6B585B89-0A6C-434E-B2BB-05495FCC880B wds:Q34549321-0C0728C5-0B3C-4CC0-8552-5FE0FBA020AE

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