About: A new general method of homolytic alkylation of protonated heteroaromatic bases by carboxylic acids and iodosobenzene diacetate

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About: A new general method of homolytic alkylation of protonated heteroaromatic bases by carboxylic acids and iodosobenzene diacetate Goto Sponge NotDistinct Permalink

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Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в січні 1989 (uk) im Januar 1989 veröffentlichter wissenschaftlicher Artikel (de)
publication date	wds:Q63385850-A5935F96-E27A-4938-B90C-2DBAFA7F4FD0
publication date	1989-01-01 00:00:00Z (xsd:dateTime)
cites work	wds:Q63385850-1955204C-93C2-4911-B8AB-3EDF9DBEF2D7 wds:Q63385850-749AED65-2633-4D98-8B85-808C4B6035C9
cites work	Nucleophilic character of alkyl radicals—VI Recent aspects of homolytic aromatic substitutions
author name string	wds:Q63385850-51805BD6-0588-4EF2-A3B6-5254F51D278D wds:Q63385850-81C6AC6D-5734-4A91-BD67-B49997C1BF7B wds:Q63385850-8BFBBAFC-50EE-48FD-AC0C-28A3BC44A874 wds:Q63385850-97B32235-7EAF-46AB-848B-02D5BC3255BC
author name string	Francesca Fontana Francesco Minisci Elena Vismara Maria Claudia Nogueira Barbosa
rdfs:label	A new general method of homolytic alkylation of protonated heteroaromatic bases by carboxylic acids and iodosobenzene diacetate (en) A new general method of homolytic alkylation of protonated heteroaromatic bases by carboxylic acids and iodosobenzene diacetate (nl)
skos:prefLabel	A new general method of homolytic alkylation of protonated heteroaromatic bases by carboxylic acids and iodosobenzene diacetate (en) A new general method of homolytic alkylation of protonated heteroaromatic bases by carboxylic acids and iodosobenzene diacetate (nl)
name	A new general method of homolytic alkylation of protonated heteroaromatic bases by carboxylic acids and iodosobenzene diacetate (en) A new general method of homolytic alkylation of protonated heteroaromatic bases by carboxylic acids and iodosobenzene diacetate (nl)
title	wds:Q63385850-AA66A87D-51A8-444D-B143-39AA7B80C71A
title	A new general method of homolytic alkylation of protonated heteroaromatic bases by carboxylic acids and iodosobenzene diacetate (en)
page(s)	wds:Q63385850-512C14E6-C666-4063-9A4C-E5B3EABED4B0
page(s)	4569-4572
instance of	wds:Q63385850-85EF5F99-29FD-48EC-BF0A-C43B5821B3A5
instance of	scholarly article
main subject	wds:Q63385850-C410C827-2C15-4413-8BBE-7E91D7C75733
main subject	drug discovery
published in	wds:Q63385850-226E73D2-43E7-4E6E-A32E-BCDBB94D3DE9
published in	Tetrahedron Letters
issue	wds:Q63385850-CBF410D3-0BE1-4D4E-AB15-D343680E0E33
volume	wds:Q63385850-51B93A33-33ED-41BB-AF01-0E418FB4C5E3
issue	34
volume	30
DOI	wds:Q63385850-0D097BAA-8ACB-4418-9251-810F11E62926
DOI	http://dx.doi.org/10.1016/S0040-4039(01)80747-4
DOI	10.1016/S0040-4039(01)80747-4
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q63385850
is cites work of	Decarboxylative sp C-N coupling via dual copper and photoredox catalysis A novel and mild source of carbon-centered radicals by iodosobenzene diacetate (IBDA) and sodium azide from alcohols, ethers, aldehydes, amides and alkyl iodides Copper-mediated synthesis of drug-like bicyclopentanes
is cites work of	wds:Q59060139-4FD50E9F-E81E-44F4-A41F-0FCC55E7C43D wds:Q63385843-1CAB2545-3298-4A8E-B88D-FFACE3DF869C wds:Q89745185-9F06945C-A0B5-400B-9EA6-0B44F5033C4E

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