Issue 33, 2001
From the journal:

CrystEngComm

Hideko Koshima,*a   Daisuke Matsushigea  and  Masashi Miyauchia  

* Corresponding authors

a Department of Applied Chemistry, Faculty of Engineering, Ehime University, Matsuyama, Japan
E-mail: koshima@en3.ehime-u.ac.jp

Abstract

A salt crystal of 2,5-diisopropyl-4′-carboxybenzophenone and (S)-phenylethylamine underwent enantiospecific photocyclization via single crystal-to-single crystal transformation to give (R)-(+)-cyclobutenol in almost quantitative optical yield and 100% chemical yield.

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Article information

DOI
https://doi.org/10.1039/B103517G
Article type
Paper
Submitted
19 Apr 2001
Accepted
27 Jun 2001

CrystEngComm, 2001,3, 141-143

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Enantiospecific single crystal-to-single crystal photocyclization of 2,5-diisopropyl-4′-carboxybenzophenone in the salt crystals with (S)- and (R)-phenylethylamine

H. Koshima, D. Matsushige and M. Miyauchi, CrystEngComm, 2001, 3, 141 DOI: 10.1039/B103517G

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