r37980778c78--3e87a11e02d29486b799ca31fc3a1a4c

Chemical syntheses of two stereochemically unique resveratrol dimers, caraphenols B and C, have shown that their structures are misassigned. Thoughts on their potential chemical etiology led to an alternate structural proposal that has been confirmed through synthesis, one indicating that the substituents on their respective indane systems exist in a relative trans,trans orientation rather than the originally postulated all-cis arrangement.

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/ol2022406.s004
URL https://figshare.com/articles/Structural_Revision_and_Total_Synthesis_of_Caraphenol_B_and_C/2597737
URL http://dx.doi.org/10.1021/ol2022406.s004
Access Modality

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

Field Value
Access Right Open Access
Publishing

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

Field Value
Collected From figshare
Hosted By figshare
Publication Date 2016-02-22
Additional Info
Field Value
Language UNKNOWN
Resource Type Dataset
system:type dataset
Management Info
Field Value
Source https://science-innovation-policy.openaire.eu/search/dataset?datasetId=r37980778c78::3e87a11e02d29486b799ca31fc3a1a4c
Author jsonws_user
Last Updated 1 January 2021, 01:41 (CET)
Created 1 January 2021, 01:41 (CET)