About: A novel and efficient route to (E)-alk-1-enyl boronic acid derivatives from (E)-1-(trimethylsilyl)alk-1-enes and a formal Suzuki–Miyaura cross-coupling reaction starting with vinylsilanes

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About: A novel and efficient route to (E)-alk-1-enyl boronic acid derivatives from (E)-1-(trimethylsilyl)alk-1-enes and a formal Suzuki–Miyaura cross-coupling reaction starting with vinylsilanes Goto Sponge NotDistinct Permalink

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Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в 1995 (uk) article scientifique publié en 1995 (fr) im Jahr 1995 veröffentlichter wissenschaftlicher Artikel (de)
publication date	wds:Q62396307-3393D4CB-3BDE-4A5C-9002-84FC15EF4619
publication date	1995-01-01 00:00:00Z (xsd:dateTime)
cites work	wds:Q62396307-004B2590-FED4-40C4-8DCB-C57D0149C84C wds:Q62396307-020D5D48-3B64-498B-AB38-AD8496B250E8 wds:Q62396307-47016C2A-471B-44E0-9AAD-8761EC9B525F wds:Q62396307-4C00D112-92F4-4447-B0A7-38683B896E22 wds:Q62396307-7529D759-DF1A-442C-A5F5-E67BA29A38BF wds:Q62396307-9D7393BC-9CE1-44FF-B444-367FEB3D046A wds:Q62396307-F968CF07-EE4E-4FAE-BF84-77CC0DEC5221
cites work	Synthetic studies via the cross-coupling reaction of organoboron derivatives with organic halides A general approach to conjugated (E,E)-dienes through sequential coupling reactions A new straightforward and general approach to dienamide natural products An Easy Route to Conjugated (allE) Tetraene Compounds via Disilyl Derivatives Exemplified by β-Parinaric Acid Methyl Ester A new approach to silylated ketones and dicarbonyl compounds with a conjugated (all E) diene or triene structure Catecholborane (1,3,2-benzodioxaorole) as a new, general monohydroboration reagent for alkynes. Convenient synthesis of alkeneboronic esters and acids from alkynes via hydroboration The Electrophilic Substitution of Allylsilanes and Vinylsilanes
author name string	wds:Q62396307-5EA55F0E-4C4E-4618-9F0C-4B8440C1A8DC wds:Q62396307-875A4827-AB5F-4082-801D-4AACA26012E0 wds:Q62396307-B31ADD90-496A-4CA8-BE8C-4A719FA31534 wds:Q62396307-CB2F30DE-BFD1-4DDD-B10A-42859C289926
author name string	Francesco Naso Gianluca M. Farinola Vito Fiandanese Luigia Mazzone
rdfs:label	A novel and efficient route to (E)-alk-1-enyl boronic acid derivatives from (E)-1-(trimethylsilyl)alk-1-enes and a formal Suzuki–Miyaura cross-coupling reaction starting with vinylsilanes (en) A novel and efficient route to (nl)
skos:prefLabel	A novel and efficient route to (E)-alk-1-enyl boronic acid derivatives from (E)-1-(trimethylsilyl)alk-1-enes and a formal Suzuki–Miyaura cross-coupling reaction starting with vinylsilanes (en) A novel and efficient route to (nl)
name	A novel and efficient route to (E)-alk-1-enyl boronic acid derivatives from (E)-1-(trimethylsilyl)alk-1-enes and a formal Suzuki–Miyaura cross-coupling reaction starting with vinylsilanes (en) A novel and efficient route to (nl)
title	wds:Q62396307-088FA097-49F7-4FA4-B5CA-14126EB23A66
title	A novel and efficient route to (E)-alk-1-enyl boronic acid derivatives from (E)-1-(trimethylsilyl)alk-1-enes and a formal Suzuki–Miyaura cross-coupling reaction starting with vinylsilanes (en)
page(s)	wds:Q62396307-55A83A75-4FDA-40F8-95CA-213BA485BDB1
page(s)	2523-2524
instance of	wds:Q62396307-E659A946-9B58-4DE2-9401-DE319D654728
instance of	scholarly article
published in	wds:Q62396307-1AEFEA66-D7EA-44CF-B5C4-61E922D20381
published in	Journal of the Chemical Society. Chemical communications
issue	wds:Q62396307-9439FF38-634C-4C44-96A2-3459E5CBF351
issue	24
DOI	wds:Q62396307-33E37561-D5E5-4FCF-A27A-5F68553DC8D6
DOI	http://dx.doi.org/10.1039/C39950002523
DOI	10.1039/C39950002523
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q62396307
is cites work of	Recent advances in the cross-coupling reactions of organoboron derivatives with organic electrophiles, 1995–1998 A straightforward route to polyenylsilanes by palladium- or nickel-catalyzed cross-coupling reactions Pd-Promoted Homocoupling Reactions of Unsaturated Silanes in Aqueous Micelles
is cites work of	wds:Q57718714-A0597544-6DF5-4E4E-B7B5-EB30B6E2DB5F wds:Q56482589-28EBDA41-2606-46EF-AA53-B751F0DA9AC3 wds:Q62396292-52AE72D3-7CE7-4690-9E57-DC421CBF750D

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