About: PINDY: A novel, pinene-derived bipyridine ligand and its application in asymmetric, Copper(I)-catalyzed allylic oxidation

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About: PINDY: A novel, pinene-derived bipyridine ligand and its application in asymmetric, Copper(I)-catalyzed allylic oxidation Goto Sponge NotDistinct Permalink

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scientific article published on 01 October 2000

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в жовтні 2000 (uk) article scientifique publié en 2000 (fr) im Oktober 2000 veröffentlichter wissenschaftlicher Artikel (de) artículu científicu espublizáu n'ochobre de 2000 (ast) scientific article published on 01 October 2000 (en)
publication date	wds:Q73014814-5F8F9F34-1871-4511-A3E3-EE3FB7EA9441
publication date	2000-10-01 00:00:00Z (xsd:dateTime)
author name string	wds:Q73014814-05F5FF55-DE8A-4C41-8619-6EB9D04C7ED7 wds:Q73014814-45874D91-989D-46DE-AFAD-9E7B4747CEA0 wds:Q73014814-D746598D-A857-4DE1-957B-572D82F18046
author name string	Bella M Langer V V Malkov AV
rdfs:label	PINDY: A novel, pinene-derived bipyridine ligand and its application in asymmetric, Copper(I)-catalyzed allylic oxidation (en) PINDY: A novel, pinene-derived bipyridine ligand and its application in asymmetric, Copper(I)-catalyzed allylic oxidation (nl)
skos:prefLabel	PINDY: A novel, pinene-derived bipyridine ligand and its application in asymmetric, Copper(I)-catalyzed allylic oxidation (en) PINDY: A novel, pinene-derived bipyridine ligand and its application in asymmetric, Copper(I)-catalyzed allylic oxidation (nl)
name	PINDY: A novel, pinene-derived bipyridine ligand and its application in asymmetric, Copper(I)-catalyzed allylic oxidation (en) PINDY: A novel, pinene-derived bipyridine ligand and its application in asymmetric, Copper(I)-catalyzed allylic oxidation (nl)
author	wds:Q73014814-6F437389-0BE9-4B27-98A8-3483408BC1BC
author	Pavel Kocovsky
title	wds:Q73014814-7D9A5851-7F97-45C1-A9E5-2F6E03D54A81
title	PINDY: A novel, pinene-derived bipyridine ligand and its application in asymmetric, Copper(I)-catalyzed allylic oxidation (en)
page(s)	wds:Q73014814-9E673DD3-BA62-4F00-AA89-DB1B09040D98
page(s)	3047-3049
instance of	wds:Q73014814-25BE3921-FEF5-49B4-9389-113C0DE23841
instance of	scholarly article
PubMed ID	wds:Q73014814-5460A118-C380-4137-9EC9-731A098CCE0A
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/11009342
PubMed ID	11009342
published in	wds:Q73014814-73EB1088-1DD6-4A72-834A-BB0C1B102055
published in	Organic Letters
issue	wds:Q73014814-334B2B25-2559-4F90-AC21-189457DBDFBE
volume	wds:Q73014814-2FB9B268-8DFD-4152-907A-1ADE58348911
issue	20
volume	2
DOI	wds:Q73014814-E4CC5DFD-334B-49B2-85D6-A9A9D05339B4
DOI	http://dx.doi.org/10.1021/OL006111K
DOI	10.1021/OL006111K
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q73014814
is cites work of	Catalytic Asymmetric Intermolecular Allylic Functionalization of Unactivated Internal Alkenes. A Chiral Nitrogen Ligand for Enantioselective, Iridium-Catalyzed Silylation of Aromatic C-H Bonds Synthetic routes for a new family of chiral tetradentate ligands containing pyridine rings 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
is cites work of	wds:Q55692192-64D26B96-C4CC-4113-8D3B-988ACE2A4AAD wds:Q30821412-2139DA03-8555-4BDA-A2E1-F0C8BB23F07D wds:Q46075345-20FD37A4-1994-4A6C-B773-BF051902D140 wds:Q58682243-79C5D383-EC12-4F18-9901-8AA287585B56

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