About: Enantioselective Diels-Alder reaction of simple alpha,beta-unsaturated ketones with a cinchona alkaloid catalyst

Facets (new session)
Description
Metadata
Settings
- owl:sameAs
- Inference Rule:

About: Enantioselective Diels-Alder reaction of simple alpha,beta-unsaturated ketones with a cinchona alkaloid catalyst Goto Sponge Distinct Permalink

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

scientific article published on 06 February 2008

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в лютому 2008 (uk) artículu científicu espublizáu en febreru de 2008 (ast) scientific article published on 06 February 2008 (en)
publication date	wds:Q80636898-A2BA3640-214E-488D-AD9C-7141368B3049
publication date	2008-02-06 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q80636898-EAF9AD31-57BF-409B-9A4E-B82EC112DFF9
language of work or name	English
author name string	wds:Q80636898-16E596F3-E90B-44C4-84D6-7BEF54AF7E15 wds:Q80636898-25813C6B-F1CF-4018-A770-AEDD4E6C1B5A wds:Q80636898-47CD82E3-D863-4A8B-8715-918838A718BE wds:Q80636898-4968193C-841A-48B4-B52A-D212496CFC6E wds:Q80636898-6A4BE383-5E0A-4442-B244-B1E81A279DDB
author name string	Ravi P Singh Li Deng Xiaojie Lu Heng Su Keith Bartelson
rdfs:label	Enantioselective Diels-Alder reaction of simple alpha,beta-unsaturated ketones with a cinchona alkaloid catalyst (en) Enantioselective Diels-Alder reaction of simple alpha,beta-unsaturated ketones with a cinchona alkaloid catalyst (nl)
skos:prefLabel	Enantioselective Diels-Alder reaction of simple alpha,beta-unsaturated ketones with a cinchona alkaloid catalyst (en) Enantioselective Diels-Alder reaction of simple alpha,beta-unsaturated ketones with a cinchona alkaloid catalyst (nl)
name	Enantioselective Diels-Alder reaction of simple alpha,beta-unsaturated ketones with a cinchona alkaloid catalyst (en) Enantioselective Diels-Alder reaction of simple alpha,beta-unsaturated ketones with a cinchona alkaloid catalyst (nl)
author	wds:Q80636898-F7AB60B5-0159-4215-A076-7D6D88FBAB7F
author	Yi Wang
title	wds:Q80636898-2DC26370-6AE2-4F05-93C1-FF35167A5DE8
title	Enantioselective Diels-Alder reaction of simple alpha,beta-unsaturated ketones with a cinchona alkaloid catalyst (en)
page(s)	wds:Q80636898-98DC6F67-21A3-4329-9CB6-7CE58FF81959
page(s)	2422-2423
instance of	wds:Q80636898-7C23E647-A6BD-4948-BDED-1C429CBC4C62
instance of	scholarly article
main subject	wds:Q80636898-2091D2B7-BBC9-4DF7-9E53-37B70920294D
main subject	enantioselectivity
PubMed ID	wds:Q80636898-B5351B43-121D-4250-83B1-53A5DD5B47B7
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/18251543
PubMed ID	18251543
published in	wds:Q80636898-5A8F1540-7396-45E4-A4C1-C163D105985A
published in	Journal of the American Chemical Society
issue	wds:Q80636898-25167A8E-7AFC-45A7-A379-46A81E46EDF0
volume	wds:Q80636898-D2AEC7B8-7E4B-4AE9-91D9-F2BEBD23B24B
issue	8
volume	130
DOI	wds:Q80636898-E3F82995-32BD-41A5-B1B1-BE8247D72146
DOI	http://dx.doi.org/10.1021/JA078251W
DOI	10.1021/JA078251W
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q80636898
is cites work of	Enantioselective organocatalytic α-fluorination of cyclic ketones Catalytic enantioselective peroxidation of alpha,beta-unsaturated ketones Catalytic asymmetric epoxidation of cyclic enones Enantioselective formal aza-Diels-Alder reactions of enones with cyclic imines catalyzed by primary aminothioureas Chiral squaramide derivatives are excellent hydrogen bond donor catalysts Catalytic Asymmetric [4 + 2] Additions with Aliphatic Nitroalkenes Chiral NHC-catalyzed oxodiene Diels-Alder reactions with alpha-chloroaldehyde bisulfite salts Asymmetric aza-Michael reactions of alpha,beta-unsaturated ketones with bifunctional organic catalysts Catalytic asymmetric hydroperoxidation of alpha,beta-unsaturated ketones: an approach to enantiopure peroxyhemiketals, epoxides, and aldols Construction of bispirooxindoles containing three quaternary stereocentres in a cascade using a single multifunctional organocatalyst. Primary-Amine-Catalyzed Enantioselective Intramolecular Aldolizations Asymmetric Synthesis of [2.2.2]-Bicyclic Lactones via All-Carbon Inverse-Electron-Demand Diels-Alder Reaction Asymmetric approach toward chiral cyclohex-2-enones from anisoles via an enantioselective isomerization by a new chiral diamine catalyst Mechanism and selectivity of cinchona alkaloid catalyzed [1,3]-shifts of allylic trichloroacetimidates Cinchona alkaloid catalyzed enantioselective amination of α,β-unsaturated ketones: an asymmetric approach to Δ(2)-pyrazolines Strong and Confined Acids Control Five Stereogenic Centers in Catalytic Asymmetric Diels-Alder Reactions of Cyclohexadienones with Cyclopentadiene
is cites work of	wds:Q33797177-4F4897AC-CCF9-487A-A683-DB5F5768E493 wds:Q37120806-34B67D50-B12A-4738-A11B-C2B9C65F8C4B wds:Q46636872-720E17AD-3BCA-4ED7-AC31-3D7E9395AB68 wds:Q89743882-A8C1C8E5-0566-4CEC-9DB0-3BCD37249CE7 wds:Q37240683-125A3F53-A79C-4B35-94B5-F8A72F03DF1E wds:Q41856190-DA9E6DA4-FAFC-4533-9262-8F1A0937665D wds:Q90233406-9749D88B-80E2-4370-A1AD-8A0BD7A3F9B6 wds:Q37357445-05C3BCED-A95D-4569-96D9-5B1B1884B0FE wds:Q37309821-C2C7D6B4-7CD2-4D8E-B9A3-C3E4D41117D5 wds:Q35607000-3CC4A0E6-8B6F-4D7D-9041-C4EEE67D54C4 wds:Q82054147-30063C96-97ED-4EE2-9A03-4B56E3853CAA wds:Q36381329-A3A9623A-0D01-4D44-9BEC-BD55130F2328 wds:Q37120775-D5D11F37-3C03-4733-97D7-C170D8237005 wds:Q36954622-5D75FEB1-87C0-4B3D-AE27-5F27A80F4D78 wds:Q46008342-FC886BA6-0C21-48F1-8765-D407C7DE6B1E wds:Q58173088-D0851C51-2261-4BD5-87FC-0B18D71EB866

Faceted Search & Find service v1.16.117 as of May 05 2024

Alternative Linked Data Documents: ODE Content Formats:

RDF

ODATA

Microdata

About

OpenLink Virtuoso version 07.20.3239 as of May 5 2024, on Linux (x86_64-centos_6-linux-gnu), Single-Server Edition (378 GB total memory, 194 GB memory in use)
Data on this page belongs to its respective rights holders.
Virtuoso Faceted Browser Copyright © 2009-2024 OpenLink Software