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On the use of seven-membered phosphorous heterocycles based on 2,2′-dihydroxy-1,1′-binaphthalene and 1,4∶3,6-dianhydro-d-mannitol in the31P NMR analysis of the enantiomeric composition of chiral alcohols

On the use of seven-membered phosphorous heterocycles based on 2,2′-dihydroxy-1,1′-binaphthalene... Some aspects of phosphorylation of 2,2′-dihydroxy-1,1′-binaphthalene (BINOL) and 1,4∶3,6-dianhydro-d-mannitol (isomannide) were investigated. The possibility of using the corresponding cyclic chloro- and amidophosphites for the analysis of enantiomeric compositions of chiral primary and secondary alcohols by31P NMR was examined. http://www.deepdyve.com/assets/images/DeepDyve-Logo-lg.png Russian Chemical Bulletin Springer Journals

On the use of seven-membered phosphorous heterocycles based on 2,2′-dihydroxy-1,1′-binaphthalene and 1,4∶3,6-dianhydro-d-mannitol in the31P NMR analysis of the enantiomeric composition of chiral alcohols

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References (14)

Publisher
Springer Journals
Copyright
Copyright © 1998 by Plenum Publishing Corporation
Subject
Chemistry; Chemistry/Food Science, general; Inorganic Chemistry; Organic Chemistry
ISSN
1066-5285
eISSN
1573-9171
DOI
10.1007/BF02495644
Publisher site
See Article on Publisher Site

Abstract

Some aspects of phosphorylation of 2,2′-dihydroxy-1,1′-binaphthalene (BINOL) and 1,4∶3,6-dianhydro-d-mannitol (isomannide) were investigated. The possibility of using the corresponding cyclic chloro- and amidophosphites for the analysis of enantiomeric compositions of chiral primary and secondary alcohols by31P NMR was examined.

Journal

Russian Chemical BulletinSpringer Journals

Published: Aug 31, 2006

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