About: 3,3‘-Bis(diphenylphosphino)-1,1‘-disubstituted-2,2‘-biindoles: Easily Accessible, Electron-Rich, Chiral Diphosphine Ligands for Homogeneous Enantioselective Hydrogenation of Oxoesters

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About: 3,3‘-Bis(diphenylphosphino)-1,1‘-disubstituted-2,2‘-biindoles: Easily Accessible, Electron-Rich, Chiral Diphosphine Ligands for Homogeneous Enantioselective Hydrogenation of Oxoesters Goto Sponge NotDistinct Permalink

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scientific article published on 01 December 2000

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в грудні 2000 (uk) im Dezember 2000 veröffentlichter wissenschaftlicher Artikel (de) artículu científicu espublizáu n'avientu de 2000 (ast) scientific article published on 01 December 2000 (en)
publication date	wds:Q61393810-75DC9633-8169-4F73-A782-946CBFAF62BF
publication date	2000-12-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q61393810-EF7232C6-2035-4B83-9147-F7B2F27F2D42
language of work or name	English
author name string	wds:Q61393810-409CE556-4854-48EF-898C-29567C34304D wds:Q61393810-822AA8AF-D6CA-444F-9DD0-ECF67F89B277
author name string	Piccolo O Sannicolo F
rdfs:label	3,3‘-Bis(diphenylphosphino)-1,1‘-disubstituted-2,2‘-biindoles: Easily Accessible, Electron-Rich, Chiral Diphosphine Ligands for Homogeneous Enantioselective Hydrogenation of Oxoesters (en) 3,3‘-Bis(diphenylphosphino)-1,1‘-disubstituted-2,2‘-biindoles: Easily Accessible, Electron-Rich, Chiral Diphosphine Ligands for Homogeneous Enantioselective Hydrogenation of Oxoesters (nl)
skos:prefLabel	3,3‘-Bis(diphenylphosphino)-1,1‘-disubstituted-2,2‘-biindoles: Easily Accessible, Electron-Rich, Chiral Diphosphine Ligands for Homogeneous Enantioselective Hydrogenation of Oxoesters (en) 3,3‘-Bis(diphenylphosphino)-1,1‘-disubstituted-2,2‘-biindoles: Easily Accessible, Electron-Rich, Chiral Diphosphine Ligands for Homogeneous Enantioselective Hydrogenation of Oxoesters (nl)
name	3,3‘-Bis(diphenylphosphino)-1,1‘-disubstituted-2,2‘-biindoles: Easily Accessible, Electron-Rich, Chiral Diphosphine Ligands for Homogeneous Enantioselective Hydrogenation of Oxoesters (en) 3,3‘-Bis(diphenylphosphino)-1,1‘-disubstituted-2,2‘-biindoles: Easily Accessible, Electron-Rich, Chiral Diphosphine Ligands for Homogeneous Enantioselective Hydrogenation of Oxoesters (nl)
author	wds:Q61393810-2786AC57-AAC2-442D-84B0-1F18C5E99418 wds:Q61393810-79369373-78E5-4B08-9B8D-7085A90D0D67
author	Tiziana Benincori Simona Rizzo
title	wds:Q61393810-0888F822-3FD5-46BB-AABA-6CB0A5946E62
title	3,3'-Bis(diphenylphosphino)-1,1'-disubstituted-2,2'-biindoles: easily accessible, electron-rich, chiral diphosphine ligands for homogeneous enantioselective hydrogenation of oxoesters (en)
page(s)	wds:Q61393810-48096C7D-9E60-4747-9423-FD90C1A9B61E
page(s)	8340-8347
instance of	wds:Q61393810-2AD693AA-64F3-47FF-990C-982F1FA7E9F3
instance of	scholarly article
main subject	wds:Q61393810-0EC033F4-3C43-472B-955A-674DDAC5095B wds:Q61393810-78C8C69D-9694-4281-B5E3-AD2AFBF64CD4
main subject	chirality enantioselectivity
PubMed ID	wds:Q61393810-5C38326A-EB81-45B6-ADA2-07967068B1FA
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/11101394
PubMed ID	11101394
published in	wds:Q61393810-DFA9DDAF-9BB7-474E-88B5-267CC31528C1
published in	Journal of Organic Chemistry
issue	wds:Q61393810-3719C3DF-371D-44D7-8A55-F295A33E3181
volume	wds:Q61393810-55706237-FFEE-4EE1-AD61-7254CB616360
issue	24
volume	65
DOI	wds:Q61393810-0825EE32-4FF0-40A9-96F4-4A2A221FB0D0
DOI	http://dx.doi.org/10.1021/JO001207D
DOI	10.1021/JO001207D
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q61393810
is cites work of	Structure-activity relationship of imidazopyridinium analogues as antagonists of neuropeptide s receptor Effects of the electronic properties of chiral chelating diphosphines in stereoselective Diels–Alder cycloaddition reactions promoted by their transition metals complexes Conversion of two stereocenters to one or two chiral axes: atroposelective synthesis of 2,3-diarylbenzoindoles On the relation between carbonyl stretching frequencies and the donor power of chelating diphosphines in nickel dicarbonyl complexes Process-Scale Total Synthesis of Nature-Identical (−)-(S,S)-7-Hydroxycalamenal in High Enantiomeric Purity through Catalytic Enantioselective Hydrogenation Discrimination of Axial and Central Stereogenic Elements in Chiral Bis(oxazolines) Based on Atropisomeric 3,3'-Bithiophene Scaffolds Through Chiroptical Spectroscopies Rational design of cyclopropane-based chiral PHOX ligands for intermolecular asymmetric Heck reaction Ph-tetraMe-Bithienine, the First Member of the Class of Chiral Heterophosphepines: Synthesis, Electronic and Steric Properties, Metal Complexes and Catalytic Activity
is cites work of	wds:Q28833640-05B2E473-368D-4B86-B8B5-DDBE2160C13B wds:Q61393771-7A36BFA8-31F5-48FD-AAEA-E6EC9F6F846F wds:Q92485855-F82CE884-E5EF-4F3F-B526-8EA06B90467F wds:Q38901722-14DB0CF5-D8B6-491A-BD84-C3944181A2DF wds:Q61393715-C1FE009B-6916-49BC-A3C4-16DAD48C1F90 wds:Q34083149-3A9B6A9C-7D90-4970-A502-E4969AE0CA54 wds:Q61393594-3DFB3807-993F-4DC6-A555-97EC2F70D374 wds:Q88419320-235E8097-3754-4BBF-92D4-43B2695AE63F

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