About: AuI-catalyzed cycloisomerization of 1,5-enynes bearing a propargylic acetate: formation of unexpected bicyclo[3.1.0]hexene

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About: AuI-catalyzed cycloisomerization of 1,5-enynes bearing a propargylic acetate: formation of unexpected bicyclo[3.1.0]hexene Goto Sponge NotDistinct Permalink

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scientific article published on 13 April 2006

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована у 2006 (uk) im Januar 2006 veröffentlichter wissenschaftlicher Artikel (de) scientific article published on 13 April 2006 (en) artículu científicu espublizáu n'abril de 2006 (ast)
publication date	wds:Q60491348-C0793AD2-5805-4585-B914-9EDD0F4A295B
publication date	2006-04-13 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q60491348-680168C2-20AB-419C-BE96-73195549CC7B
language of work or name	English
author name string	wds:Q60491348-1B1976F0-D916-4B7E-A065-6C741FF0A13B wds:Q60491348-8FF049C5-4221-4ABE-A970-A33A7B48658D
author name string	Edwin D Stevens Nicolas Marion
rdfs:label	AuI-catalyzed cycloisomerization of 1,5-enynes bearing a propargylic acetate: formation of unexpected bicyclo[3.1.0]hexene (en) AuI-catalyzed cycloisomerization of 1,5-enynes bearing a propargylic acetate: formation of unexpected bicyclo[3.1.0]hexene (nl)
skos:prefLabel	AuI-catalyzed cycloisomerization of 1,5-enynes bearing a propargylic acetate: formation of unexpected bicyclo[3.1.0]hexene (en) AuI-catalyzed cycloisomerization of 1,5-enynes bearing a propargylic acetate: formation of unexpected bicyclo[3.1.0]hexene (nl)
name	AuI-catalyzed cycloisomerization of 1,5-enynes bearing a propargylic acetate: formation of unexpected bicyclo[3.1.0]hexene (en) AuI-catalyzed cycloisomerization of 1,5-enynes bearing a propargylic acetate: formation of unexpected bicyclo[3.1.0]hexene (nl)
author	wds:Q60491348-1765B361-2E63-40AF-ABA5-D4D3C8CC1EEE wds:Q60491348-44B45C51-9F87-475F-8E48-EA3453BA6D27 wds:Q60491348-7BDA974E-2FB1-4711-8A2C-19DE8F62F77A wds:Q60491348-B3E97F3D-9B8F-48C2-8C57-C659923311CA wds:Q60491348-E43BCE05-255E-41E9-885F-14DD55154731
author	Louis Fensterbank Steven P. Nolan Max Malacria Pierre de Frémont Gilles Lemière
title	wds:Q60491348-7B17DEF1-A6C0-44B0-B0EC-726F3A053159
title	Au(I)-catalyzed cycloisomerization of 1,5-enynes bearing a propargylic acetate: formation of unexpected bicyclo[3.1.0]hexene (en)
page(s)	wds:Q60491348-8C8E734D-FD46-4148-84DC-DFAE10CCF7D9
page(s)	2048-2050
instance of	wds:Q60491348-7219891A-CA46-4FEE-A6E5-B5EF0DCF9591
instance of	scholarly article
PubMed ID	wds:Q60491348-453E4E34-FC00-4BFD-8478-F37427A812B3
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/16767271
PubMed ID	16767271
published in	wds:Q60491348-52B8F769-E286-47FC-9BA6-26E0F90A4355
published in	Chemical Communications
issue	wds:Q60491348-AC8C2A16-F0FE-4748-B6C1-E378EFC7397C
issue	19
DOI	wds:Q60491348-3F01060C-3966-4A0C-A892-993CC165FEC0
DOI	http://dx.doi.org/10.1039/B602839J
DOI	10.1039/B602839J
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q60491348
is cites work of	Ligand effects in homogeneous Au catalysis Gold(I)-Catalyzed Activation of Alkynes for the Construction of Molecular Complexity. Samb V ca: A Web Application for the Calculation of the Buried Volume of N-Heterocyclic Carbene Ligands Asymmetric syntheses of 8-oxabicyclo[3,2,1]octane and 11-oxatricyclo[5.3.1.0]undecane from glycals Electronic effects in the pt-catalyzed cycloisomerization of propargylic esters: synthesis of 2,3-disubstituted indolizines as a mechanistic probe Gold(I)-catalyzed dearomative Rautenstrauch rearrangement: enantioselective access to cyclopenta[b]indoles Scope and limitations of the dual-gold-catalysed hydrophenoxylation of alkynes A porphyrin complex of gold(I): (phosphine)gold(I) azides as cation precursors Au-Catalyzed Hexannulation and Pt-Catalyzed Pentannulation of Propargylic Ester Bearing a 2-Alkynyl-phenyl Substituent: A Comparative DFT Study Novel Benzyl- or 4-Cyanobenzyl-Substituted N-Heterocyclic (Bromo)(carbene)silver(I) and (Carbene)(chloro)gold(I) Complexes: Synthesis and Preliminary Cytotoxicity Studies NHC-containing chiral bidentate ligands: synthesis and evaluation in enantioselective copper-catalyzed conjugate addition
is cites work of	wds:Q42285500-B05649F3-6C92-47AC-A8EB-79D7B91F1946 wds:Q37225816-7A86FD2C-2A0E-406F-8451-A10C7DEBB41D wds:Q41625219-70248A05-7FCF-4459-99CD-914E104A31BE wds:Q38781751-0412EA17-D1A2-42E8-B8F2-341A6ED8ECAE wds:Q92931233-80D324D9-55FC-41FE-910C-4B468778B9E5 wds:Q42145210-DD788A6B-6E3A-4FFB-AC61-07417690EAB3 wds:Q36936385-2D39113F-68FB-485A-B9B0-9DBB61EA837A wds:Q80060158-3FB72C9E-8DAA-4E5B-91BC-CA35274E1A21 wds:Q41962217-248E73C1-E166-4BA9-A584-7FC1CED9E81C wds:Q27144118-F2E56973-2F68-40DB-B273-D82F0F466E40 wds:Q59867850-D20552A5-8066-42D6-AB13-BE17B56B5ACB

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