About: Gold carbenes via 1,2-dialkoxycyclopropane ring-opening: a mass spectrometric and DFT study of the reaction pathways

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About: Gold carbenes via 1,2-dialkoxycyclopropane ring-opening: a mass spectrometric and DFT study of the reaction pathways Goto Sponge NotDistinct Permalink

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scientific article published on 20 April 2010

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована у 2010 (uk) im Januar 2010 veröffentlichter wissenschaftlicher Artikel (de) scientific article published on 20 April 2010 (en) artículu científicu espublizáu n'abril de 2010 (ast)
publication date	wds:Q59938647-2BDDEBDA-C911-4698-A961-5873AD857849
publication date	2010-04-20 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q59938647-BD5720B0-8753-444C-9982-A62D0D18F069
language of work or name	English
author name string	wds:Q59938647-594ED956-559F-4095-8937-9D9C29E2A84B
author name string	Laurent Batiste
rdfs:label	Gold carbenes via 1,2-dialkoxycyclopropane ring-opening: a mass spectrometric and DFT study of the reaction pathways (en) Gold carbenes via 1,2-dialkoxycyclopropane ring-opening: a mass spectrometric and DFT study of the reaction pathways (nl)
skos:prefLabel	Gold carbenes via 1,2-dialkoxycyclopropane ring-opening: a mass spectrometric and DFT study of the reaction pathways (en) Gold carbenes via 1,2-dialkoxycyclopropane ring-opening: a mass spectrometric and DFT study of the reaction pathways (nl)
name	Gold carbenes via 1,2-dialkoxycyclopropane ring-opening: a mass spectrometric and DFT study of the reaction pathways (en) Gold carbenes via 1,2-dialkoxycyclopropane ring-opening: a mass spectrometric and DFT study of the reaction pathways (nl)
author	wds:Q59938647-27051A9B-8990-4D00-BF19-8ADD5C182FEF wds:Q59938647-BF75808B-243C-4E05-8928-D80B0F67A45C
author	Peter Chen Alexey Fedorov
title	wds:Q59938647-DB519A38-B26F-4A6E-BD63-CB8052064D8F
title	Gold carbenes via 1,2-dialkoxycyclopropane ring-opening: a mass spectrometric and DFT study of the reaction pathways (en)
page(s)	wds:Q59938647-5A9AAEEB-E5CC-4687-97C3-929130A00F0F
page(s)	3899-3901
instance of	wds:Q59938647-617FF550-4825-4DB6-A51E-17A2AAE03770
instance of	scholarly article
PubMed ID	wds:Q59938647-D5D1F030-0B81-4A1D-8514-7BEC40B3AA79
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/20405086
PubMed ID	20405086
published in	wds:Q59938647-6A9D27FE-139D-421A-8875-0D1F1079FB6F
published in	Chemical Communications
issue	wds:Q59938647-7DCE59A0-E437-4115-A1CC-E8CB8B9907F6
volume	wds:Q59938647-AB913A3F-E5DD-44CE-A6B3-8CA41BC5CB82
issue	22
volume	46
DOI	wds:Q59938647-5B135A34-2E13-4E8B-A362-28349D6FBECC
DOI	http://dx.doi.org/10.1039/C0CC00086H
DOI	10.1039/C0CC00086H
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q59938647
is cites work of	Gold-catalyzed rearrangements and beyond Stereoselective cis-Vinylcyclopropanation via a Gold(I)-Catalyzed Retro-Buchner Reaction under Mild Conditions Gold(I) carbenes by retro-Buchner reaction: generation and fate Gold carbene or carbenoid: is there a difference? Cyclobutene vs 1,3-Diene Formation in the Gold-Catalyzed Reaction of Alkynes with Alkenes: The Complete Mechanistic Picture.
is cites work of	wds:Q42042870-4325CEDD-748E-4759-876E-FF1FF50DA8C6 wds:Q38391525-A2ED00F4-2A4E-41A0-A052-5C56F5478EA4 wds:Q41246705-3BE41D77-275B-4E7D-8285-3D1ADB95E42D wds:Q41885109-D9B8CF34-C702-4F44-9BF4-AA800B42A972 wds:Q43170746-D7E82F17-F876-466C-AA03-1AED5C382CD7

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