Literature DB >> 31762284

One-Pot Absolute Stereochemical Identification of Alcohols via Guanidinium Sulfate Crystallization.

Beau R Brummel1, Kinsey G Lee1, Colin D McMillen1, Joseph W Kolis1, Daniel C Whitehead1.   

Abstract

A novel technique for the absolute stereochemical determination of alcohols has been developed that uses crystallization of guanidinium salts of organosulfates. The simple one-pot, two-step process leverages facile formation of guandinium organosulfate single crystals for the straightforward determination of the absolute stereochemistry of enantiopure alcohols by means of X-ray crystallography. The strong hydrogen bonding network drives the stability of the crystal lattice and allows for a diverse range of organic alcohol substrates to be analyzed.

Entities:  

Year:  2019        PMID: 31762284     DOI: 10.1021/acs.orglett.9b03792

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  2 in total

1.  Limitations of Trifluoromethylbenzoimidazolylbenzoic Acid as a Chiral Derivatizing Agent to Assign Absolute Configuration for β-Chiral Aminoalcohols.

Authors:  Michal Kriegelstein; David Profous; Adam Přibylka; Antonín Lyčka; Petr Cankař
Journal:  ACS Omega       Date:  2022-04-04

2.  Total Synthesis of (+)-Cochlearol B by an Approach Based on a Catellani Reaction and Visible-Light-Enabled [2+2] Cycloaddition.

Authors:  Alistair D Richardson; Trenton R Vogel; Emily F Traficante; Kason J Glover; Corinna S Schindler
Journal:  Angew Chem Int Ed Engl       Date:  2022-06-23       Impact factor: 16.823

  2 in total

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