Discrimination of remote chirality of primary alcohols using 1,1′-binaphthyl-2,2′-DIYL phosphoroselenoyl chlorides as a chiral molecular tool-Reference-Cited by-同舟云学术

Discrimination of remote chirality of primary alcohols using 1,1′-binaphthyl-2,2′-DIYL phosphoroselenoyl chlorides as a chiral molecular tool

Published:2016-02-01 Issue:2 Volume:191 Page:163-173
ISSN:1042-6507
Container-title:Phosphorus, Sulfur, and Silicon and the Related Elements
language:en
Short-container-title:Phosphorus, Sulfur, and Silicon and the Related Elements

Author:

Murai Toshiaki¹²,Itoh Hikaru¹

Affiliation:

1. Department of Chemistry and Biomolecular Science, Faculty of Engineering, Gifu University, Yanagido, Gifu Japan

2. JST, ACT-C, Kawaguchi, Saitama, Japan

Publisher

Informa UK Limited

Subject

Inorganic Chemistry,Organic Chemistry,Biochemistry

Link

https://www.tandfonline.com/doi/pdf/10.1080/10426507.2015.1085050

Reference14 articles.

1. Long-Range Stereo-Relay: Relative and Absolute Configuration of 1,n-Glycols from Circular Dichroism of Liposomal Porphyrin Esters

2. For reviews, see (a) Wenzel, T. J. Discrimination of Chiral Compounds; John Wiley & Sons, Inc.: New Jersey, 2007. (b) Wenzel, T. J.; Chisholm, C. D. Prog. Nucl. Magn. Reson. Spectrosc. 2011, 59, 1–63.

3. A [5]HELOL Analogue That Senses Remote Chirality in Alcohols, Phenols, Amines, and Carboxylic Acids

4. 1,1‘-Binaphthyl-2,2‘-diyl Phosphoroselenoyl Chloride as a Chiral Molecular Tool for the Preparation of Enantiomerically Pure Alcohols and Amines

5. Synthesis and Characterization of Boron Complexes of Imidazo[1,5-a]pyridylalkyl Alcohols

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