About: New C(2)-Symmetrical 1,2-Diphosphanes for the Efficient Rhodium-Catalyzed Asymmetric Hydroboration of Styrene Derivatives We thank the Deutsche Forschungsgemeinschaft (Leibniz program), The Institut de Recherches Servier (Suresnes, France), and PPG-

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About: New C(2)-Symmetrical 1,2-Diphosphanes for the Efficient Rhodium-Catalyzed Asymmetric Hydroboration of Styrene Derivatives We thank the Deutsche Forschungsgemeinschaft (Leibniz program), The Institut de Recherches Servier (Suresnes, France), and PPG- Goto Sponge NotDistinct Permalink

An Entity of Type : wikibase:Item, within Data Space : wikidata.demo.openlinksw.com associated with source document(s)

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована у квітні 2001 (uk) im April 2001 veröffentlichter wissenschaftlicher Artikel (de)
publication date	wds:Q95350168-603C138F-69A1-43B0-84B5-E1BEFDE2AE88
publication date	2001-04-01 00:00:00Z (xsd:dateTime)
cites work	wds:Q95350168-14061AA4-8085-408F-8CC8-70433E077442 wds:Q95350168-CBCE0542-05EE-498C-B758-6A046DB8A276 wds:Q95350168-CF4740FB-E089-4698-AA4D-8F4416F76101 wds:Q95350168-FCBB654F-9DA2-4CEE-9133-221316E5BB22
cites work	Catalytic Enantioselective Hydrosilylation of Aromatic Ketones Using Rhodium Complexes of TADDOL-Derived Cyclic Phosphonites and Phosphites Catalytic asymmetric hydroboration/amination and alkylamination with rhodium complexes of 1,1'-(2-diarylphosphino-1-naphthyl)isoquinoline A Novel Easily Accessible Chiral Ferrocenyldiphosphine for Highly Enantioselective Hydrogenation, Allylic Alkylation, and Hydroboration Reactions Asymmetric modular synthesis of cylindrically chiral FerroPHOS ligands for the Rh-catalyzed asymmetric hydroboration
author name string	wds:Q95350168-B9697896-8735-456C-93A0-35553AB4EE89 wds:Q95350168-DEDA0DC6-855F-4077-9EA1-22CA6343C7AE
author name string	Florence Volant Stéphane Demay
rdfs:label	New C(2)-Symmetrical 1,2-Diphosphanes for the Efficient Rhodium-Catalyzed Asymmetric Hydroboration of Styrene Derivatives We thank the Deutsche Forschungsgemeinschaft (Leibniz program), The Institut de Recherches Servier (Suresnes, France), and PPG- (en) New C(2)-Symmetrical 1,2-Diphosphanes for the Efficient Rhodium-Catalyzed Asymmetric Hydroboration of Styrene Derivatives We thank the Deutsche Forschungsgemeinschaft (Leibniz program), The Institut de Recherches Servier (Suresnes, France), and PPG- (nl)
skos:prefLabel	New C(2)-Symmetrical 1,2-Diphosphanes for the Efficient Rhodium-Catalyzed Asymmetric Hydroboration of Styrene Derivatives We thank the Deutsche Forschungsgemeinschaft (Leibniz program), The Institut de Recherches Servier (Suresnes, France), and PPG- (en) New C(2)-Symmetrical 1,2-Diphosphanes for the Efficient Rhodium-Catalyzed Asymmetric Hydroboration of Styrene Derivatives We thank the Deutsche Forschungsgemeinschaft (Leibniz program), The Institut de Recherches Servier (Suresnes, France), and PPG- (nl)
name	New C(2)-Symmetrical 1,2-Diphosphanes for the Efficient Rhodium-Catalyzed Asymmetric Hydroboration of Styrene Derivatives We thank the Deutsche Forschungsgemeinschaft (Leibniz program), The Institut de Recherches Servier (Suresnes, France), and PPG- (en) New C(2)-Symmetrical 1,2-Diphosphanes for the Efficient Rhodium-Catalyzed Asymmetric Hydroboration of Styrene Derivatives We thank the Deutsche Forschungsgemeinschaft (Leibniz program), The Institut de Recherches Servier (Suresnes, France), and PPG- (nl)
author	wds:Q95350168-0F954C10-25FC-4869-AFF3-C1EC072D9352
author	Paul Knochel
title	wds:Q95350168-908434E9-3591-47EC-9399-E0A0C4D3E99B
title	New C(2)-Symmetrical 1,2-Diphosphanes for the Efficient Rhodium-Catalyzed Asymmetric Hydroboration of Styrene Derivatives We thank the Deutsche Forschungsgemeinschaft (Leibniz program), The Institut de Recherches Servier (Suresnes, France), and PPG-SIPSY for financial support. We thank also BASF AG (Ludwigshafen), Chemetall GmbH (Frankfurt), and Degussa-Hüls AG (Hanau) for the generous gift of chemicals (en)
page(s)	wds:Q95350168-3E2F3845-FBE9-4A5A-A776-7B62C272018B
page(s)	1235-1238
instance of	wds:Q95350168-8F7F30DA-2EF6-44CC-BBCC-7595C084C3C2
instance of	scholarly article
PubMed ID	wds:Q95350168-5BC8D211-A40D-495F-8E2F-B8EEE497C04E
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/11301435
PubMed ID	11301435
published in	wds:Q95350168-3B88982E-BE7F-4ABA-A517-8C2CE146CBE7
published in	Angewandte Chemie International Edition
issue	wds:Q95350168-A14F9300-9AE5-40A1-A26A-0F78EB27B5B9
volume	wds:Q95350168-E4776018-EEA7-446A-AA82-4DDCA4EE7E64
issue	7
volume	40
DOI	wds:Q95350168-94779E66-74D8-45CE-BEC2-B9417BF24BF0
DOI	http://dx.doi.org/10.1002/1521-3773(20010401)40:7%3C1235::AID-ANIE1235%3E3.0.CO;2-Y
DOI	10.1002/1521-3773(20010401)40:7<1235::AID-ANIE1235>3.0.CO;2-Y
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q95350168
is cites work of	Efficiency of natural bentonite versus synthetic organo(bis-silantriolates) as supports towards the heterogenisation of asymmetric hydroboration
is cites work of	wds:Q60162318-95211674-0D4F-4AD9-9B31-044CF29B994D

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