Deracemization of an Axially Chiral Biphenylic Structure in Chiral Micellar Aggregates-Reference-Cited by-同舟云学术

Deracemization of an Axially Chiral Biphenylic Structure in Chiral Micellar Aggregates

Published:1998-03-25 Issue:8 Volume:14 Page:1960-1962
ISSN:0743-7463
Container-title:Langmuir
language:en
Short-container-title:Langmuir

Author:

Borocci Stefano¹,Erba Maura¹,Mancini Giovanna¹,Scipioni Anita²

Affiliation:

1. Centro CNR di Studio sui Meccanismi di Reazione, c/o Dipartimento di Chimica, Università degli Studi di Roma “La Sapienza”, P.le A. Moro 5, 00185 Roma, Italy

2. Dipartimento di Chimica, Università degli Studi di Roma “La Sapienza”, P.le A. Moro 5, 00185 Roma, Italy

Publisher

American Chemical Society (ACS)

Subject

Electrochemistry,Spectroscopy,Surfaces and Interfaces,Condensed Matter Physics,General Materials Science

Link

https://pubs.acs.org/doi/pdf/10.1021/la971072f

Reference12 articles.

1. The term deracemization is used according to March, J.AdvancedOrganicChemistry, 4th ed.; John Wiley & Sons: New York, 1992; p 124, because we describe a process in which one enantiomer is converted to the other, thanks to the interaction with an outside optically active substance, so that a racemic mixture is converted to a mixture enriched in one enantiomer.

2. An example of spontaneous resolution by sublimation

3. (b) March, J.AdvancedOrganicChemistry, 4th ed.; John Wiley & Sons: New York, 1992; p 123.

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