Tin- and Germanium-Substituted Enol Ethers from Fischer Carbene Complexes and Group 14 Vinyl Derivatives

Trialkyltin- or trialkylgermanium-substituted enol ethers 5 and 2-alkoxy-1,3-butadienes 7 have been prepared by the reaction of Fischer carbene complexes 1−3 and 6 with vinylstannanes and -germanes 4. The opening of the metallacyclobutane intermediate by metalloid migration has been shown by using a 2,2-dideuteriated olefin.

Tags
Data and Resources
To access the resources you must log in

This item has no data

Identity

Description: The Identity category includes attributes that support the identification of the resource.

Field Value
PID https://www.doi.org/10.1021/om9703999.s001
PID https://www.doi.org/10.1021/om9703999
URL https://pubs.acs.org/doi/abs/10.1021/om9703999
URL https://pubs.acs.org/doi/pdf/10.1021/om9703999
URL https://academic.microsoft.com/#/detail/2073827057
URL http://dx.doi.org/10.1021/om9703999
URL https://figshare.com/articles/journal_contribution/Tin-_and_Germanium-Substituted_Enol_Ethers_from_Fischer_Carbene_Complexes_and_Group_14_Vinyl_Derivatives/3780189
Access Modality

Description: The Access Modality category includes attributes that report the modality of exploitation of the resource.

Field Value
Access Right Open Access
Attribution

Description: Authorships and contributors

Field Value
Author José Barluenga
Author Rosario González
Author Francisco J. Fañanás
Publishing

Description: Attributes about the publishing venue (e.g. journal) and deposit location (e.g. repository)

Field Value
Collected From figshare; Crossref; Microsoft Academic Graph
Hosted By Organometallics; figshare
Publication Date 2016-08-27
Additional Info
Field Value
Language English
Resource Type Other literature type; Article
system:type publication
Management Info
Field Value
Source https://science-innovation-policy.openaire.eu/search/publication?articleId=dedup_wf_001::be408c4c709a6a2cd2d83f30a205b0d3
Author jsonws_user
Last Updated 25 December 2020, 04:15 (CET)
Created 25 December 2020, 04:15 (CET)