About: New Applications of Bis(oxazoline) Ligands in Catalysis: Asymmetric 1,2- and 1,4-Addition of ZnR2to Carbonyl Compounds

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About: New Applications of Bis(oxazoline) Ligands in Catalysis: Asymmetric 1,2- and 1,4-Addition of ZnR2to Carbonyl Compounds Goto Sponge NotDistinct Permalink

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Attributes	Values
rdf:type	Item
description	article (en) wetenschappelijk artikel (nl) наукова стаття, опублікована в грудні 2001 (uk) im Dezember 2001 veröffentlichter wissenschaftlicher Artikel (de)
publication date	wds:Q58214395-E7BA5545-999C-4E96-A580-63411E87C9E6
publication date	2001-12-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q58214395-495CC751-EF2E-4710-BAF6-B936EACC8D3E
language of work or name	English
author name string	wds:Q58214395-71ECA6FC-F9BB-407F-A98C-BCC218F5AFCE wds:Q58214395-C8BA5BB5-85F2-4C33-98DF-4190CEBEA439 wds:Q58214395-F0C33B17-5BB2-4DF1-AF1B-8237625C2C12
author name string	A Kaiser M Seitz M Schinnerl
rdfs:label	New Applications of Bis(oxazoline) Ligands in Catalysis: Asymmetric 1,2- and 1,4-Addition of ZnR2to Carbonyl Compounds (en) New Applications of Bis(oxazoline) Ligands in Catalysis: Asymmetric 1,2- and 1,4-Addition of ZnR2to Carbonyl Compounds (nl)
skos:prefLabel	New Applications of Bis(oxazoline) Ligands in Catalysis: Asymmetric 1,2- and 1,4-Addition of ZnR2to Carbonyl Compounds (en) New Applications of Bis(oxazoline) Ligands in Catalysis: Asymmetric 1,2- and 1,4-Addition of ZnR2to Carbonyl Compounds (nl)
name	New Applications of Bis(oxazoline) Ligands in Catalysis: Asymmetric 1,2- and 1,4-Addition of ZnR2to Carbonyl Compounds (en) New Applications of Bis(oxazoline) Ligands in Catalysis: Asymmetric 1,2- and 1,4-Addition of ZnR2to Carbonyl Compounds (nl)
author	wds:Q58214395-9787C5A7-45E2-4D93-AB11-FB462B474CDF
author	Oliver Reiser
title	wds:Q58214395-E47C8150-A4F4-4FCF-91F3-D4D6BCDCE812
title	New applications of bis(oxazoline) ligands in catalysis: asymmetric 1,2- and 1,4-addition of ZnR(2) to carbonyl compounds (en)
page(s)	wds:Q58214395-A2F8FC5E-93AE-4B78-83DD-2F21ACFD03BF
page(s)	4259-4262
instance of	wds:Q58214395-E67D0F80-3C15-4074-934B-CC00DF1EE899
instance of	scholarly article
PubMed ID	wds:Q58214395-8EE9CBC9-067B-4B03-AC23-92B19BF80E1F
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/11784192
PubMed ID	11784192
published in	wds:Q58214395-518D5AAF-2C54-42C3-A84A-014F9AF9B224
published in	Organic Letters
issue	wds:Q58214395-D26C13D9-C653-47AD-A691-3C50E911A692
volume	wds:Q58214395-72078630-205B-47ED-B886-625BC6F759F0
issue	26
volume	3
DOI	wds:Q58214395-0883B27F-E429-4028-A319-2D0F98AC9E0E
DOI	http://dx.doi.org/10.1021/OL016925G
DOI	10.1021/OL016925G
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q58214395
is cites work of	Asymmetric Cu(II) catalyses for cycloaddition reactions based on π-cation or n-cation interactions Enantioselective Michael Addition Reactions Diastereoselective and enantioselective conjugate addition reactions utilizing α,β-unsaturated amides and lactams Recent advances in enantioselective copper-catalyzed 1,4-addition Total Synthesis of (2RS)-α-Tocopherol through Ni-Catalyzed 1,4-Addition to a Chromenone Intermediate High efficiency and enantioselectivity in the rh-catalyzed conjugate addition of arylboronic acids using monodentate phosphoramidites Highly enantioselective Cu-catalysed asymmetric 1,4-addition of diphenylzinc to cyclohexenone Preparation of a chiral ferrocenyl derivative containing a biphenyl unit via nickel-mediated homocoupling. Copper-Catalysed, Enantioselective Desymmetrisation ofmeso Cyclic Allylic Bis(diethyl phosphates) with Organozinc Reagents Modular amino acids-based chiral ligands for copper-catalyzed enantioselective conjugation addition of diethylzinc to cyclic enones 3-substituted BINOL Schiff bases and their reductive products for catalytic asymmetric addition of diethylzinc to aldehydes Activation of nitroaldol reactions by diethylzinc and amino alcohols or diamines as promoters
is cites work of	wds:Q56805280-B3933304-F6B0-47EF-BFB1-51338F408551 wds:Q37473046-822365C7-142D-4BDD-81A2-50AE2EA7D619 wds:Q45015370-1FA83054-CB2E-48E6-AABE-239F8F3558CA wds:Q56655932-268D44FE-1714-4FE7-97C6-06461ACEC216 wds:Q57973383-BCE69AAE-4F75-4AF5-BDA5-541781038DCE wds:Q38482449-949D879F-6C79-488D-A8B7-1A2BE1EE9B42 wds:Q84409700-E4B27BCB-8646-4648-9107-DEA7873F78BE wds:Q58214371-78A7BB97-5B98-49D6-BE37-89177FD28FFD wds:Q46704182-BAFCFD8D-2DE3-4572-A9EE-8BB8BB67AE4D wds:Q46437758-DB7FBDA9-E529-43A8-8E02-C03EC198F31F wds:Q37785751-CE30E38E-C962-4A80-9544-CDA27EC6460A wds:Q79312139-C3B796DB-1C0A-492E-876C-096099EBB984

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