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Cover Feature: Absolute Configuration Assignment from Optical Rotation Data by Means of Biphenyl Chiroptical Probes (Chem. Eur. J. 22/2019)
A central‐to‐axial chirality transfer occurring when chiral molecules are linked to flexible biphenyl probes makes it possible to assign their absolute configuration from the biphenyl twist. By employing 4,4’‐disubstituted biphenyls, the twist sign, and then the absolute configuration, can be reveal...
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Published in: | Chemistry : a European journal 2019-04, Vol.25 (22), p.5597-5597 |
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container_end_page | 5597 |
container_issue | 22 |
container_start_page | 5597 |
container_title | Chemistry : a European journal |
container_volume | 25 |
creator | Vergura, Stefania Scafato, Patrizia Belviso, Sandra Superchi, Stefano |
description | A central‐to‐axial chirality transfer occurring when chiral molecules are linked to flexible biphenyl probes makes it possible to assign their absolute configuration from the biphenyl twist. By employing 4,4’‐disubstituted biphenyls, the twist sign, and then the absolute configuration, can be revealed by the sign of optical rotation. This allows for assignment of the absolute configuration of chiral α‐substituted carboxylic acids and primary amines in a non‐empirical and straightforward way by simple [α]D measurements. More information can be found in the Full Paper by S. Superchi et al. on page 5682. |
doi_str_mv | 10.1002/chem.201901165 |
format | article |
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source | Wiley-Blackwell Read & Publish Collection |
subjects | absolute configuration biphenyls chiroptical probes circular dichroism optical rotation |
title | Cover Feature: Absolute Configuration Assignment from Optical Rotation Data by Means of Biphenyl Chiroptical Probes (Chem. Eur. J. 22/2019) |
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