About: Reactive ketenes through a carbonate/amine shuttle deprotonation strategy: catalytic, enantioselective alpha-bromination of acid chlorides

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About: Reactive ketenes through a carbonate/amine shuttle deprotonation strategy: catalytic, enantioselective alpha-bromination of acid chlorides Goto Sponge NotDistinct Permalink

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scientific article published on 01 June 2001

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в червні 2001 (uk) im Juni 2001 veröffentlichter wissenschaftlicher Artikel (de) artículu científicu espublizáu en xunu de 2001 (ast) scientific article published on 01 June 2001 (en)
publication date	wds:Q74062792-37DD11BE-B0E5-40F4-ABCD-CED299A54C0D
publication date	2001-06-01 00:00:00Z (xsd:dateTime)
author name string	wds:Q74062792-2C6E5D6D-F025-497D-A660-B624F01C7F6E wds:Q74062792-3219F903-C984-4A80-88E7-F627157C4A5E wds:Q74062792-3CA641F9-2DDF-4304-94A0-246078D41E24 wds:Q74062792-7FB5A33A-94EB-43EB-93A1-ECA59887CA35 wds:Q74062792-F25AC6E3-F4F8-4E0D-A129-2E996BCA5A70
author name string	A E Taggi H Wack T Lectka A M Hafez J Esterbrook
rdfs:label	Reactive ketenes through a carbonate/amine shuttle deprotonation strategy: catalytic, enantioselective alpha-bromination of acid chlorides (en) Reactive ketenes through a carbonate/amine shuttle deprotonation strategy: catalytic, enantioselective alpha-bromination of acid chlorides (nl)
skos:prefLabel	Reactive ketenes through a carbonate/amine shuttle deprotonation strategy: catalytic, enantioselective alpha-bromination of acid chlorides (en) Reactive ketenes through a carbonate/amine shuttle deprotonation strategy: catalytic, enantioselective alpha-bromination of acid chlorides (nl)
name	Reactive ketenes through a carbonate/amine shuttle deprotonation strategy: catalytic, enantioselective alpha-bromination of acid chlorides (en) Reactive ketenes through a carbonate/amine shuttle deprotonation strategy: catalytic, enantioselective alpha-bromination of acid chlorides (nl)
title	wds:Q74062792-984F2913-4519-48E5-9B2A-A05C3D348611
title	Reactive ketenes through a carbonate/amine shuttle deprotonation strategy: catalytic, enantioselective alpha-bromination of acid chlorides (en)
page(s)	wds:Q74062792-1ED3ED9C-09D6-4DDD-A920-790EB17C53C5
page(s)	2049-2051
instance of	wds:Q74062792-8828561D-5827-42B0-B47D-80F0D1F66BEB
instance of	scholarly article
main subject	wds:Q74062792-41FB54F1-9E26-416C-892A-EA992D341631
main subject	enantioselectivity
PubMed ID	wds:Q74062792-4EA335E1-6AB1-46CA-9EC0-F9212A1D4566
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/11418046
PubMed ID	11418046
published in	wds:Q74062792-2BF4B839-A50D-4A92-9E97-BC959362EC2C
published in	Organic Letters
issue	wds:Q74062792-8BA15643-CF19-4C2B-889A-FCD5968FCC34
volume	wds:Q74062792-11B34559-0B60-4FE4-8AD7-50E2739E0480
issue	13
volume	3
DOI	wds:Q74062792-FEE34BFC-A028-4022-B9AD-24BF7AF38A0A
DOI	http://dx.doi.org/10.1021/OL0160147
DOI	10.1021/OL0160147
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q74062792
is cites work of	Catalytic, asymmetric alpha-fluorination of acid chlorides: dual metal-ketene enolate activation. Acylammonium salts as dienophiles in Diels-Alder/lactonization organocascades. From bifunctional to trifunctional (tricomponent nucleophile-transition metal-lewis acid) catalysis: the catalytic, enantioselective α-fluorination of acid chlorides Quantum mechanical investigations of organocatalysis: mechanisms, reactivities, and selectivities Catalytic, asymmetric reactions of ketenes and ketene enolates. Asymmetric Organocatalysis: The Emerging Utility of α,β-Unsaturated Acylammonium Salts. Multiple roles of aryloxide leaving groups in enantioselective annulations employing α,β-unsaturated acyl ammonium catalysis.
is cites work of	wds:Q42322495-5FC18B81-40A3-412B-818D-E3C61E64C80D wds:Q35159601-035D5AC8-E975-4840-B3AA-DFBD9727FBC9 wds:Q38733277-EB5D287E-A8D3-464D-A07D-239F3B6C13A7 wds:Q36138930-AF6F43EB-C444-4BCD-8DDD-064A8C959E3E wds:Q43168999-63363FA5-1861-4A54-83A4-9662C0682142 wds:Q42714607-9A4527E6-5B83-4CA6-B8DC-3D0AC286044D wds:Q55410217-4E2E0212-7072-42EB-99A5-5AC02A40FF2E

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