Selective Reduction of Cyclohexanones with NaBH4 in β-Cyclodextrin, PEG-400, and Micelles-Reference-Cited by-同舟云学术

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Selective Reduction of Cyclohexanones with NaBH4 in β-Cyclodextrin, PEG-400, and Micelles

Published:2008-06-01 Issue:4 Volume:20 Page:379-385
ISSN:1061-0278
Container-title:Supramolecular Chemistry
language:en
Short-container-title:Supramolecular Chemistry

Author:

Kobetić Renata¹,Petrović-Peroković Vesna²,Ključarić Valentina³,Juršić Branko⁴,Sunko Dionis E.²

Affiliation:

1. a Department of Chemistry , Ruder Bošković Institute , Bijenička cesta 54, P.O. Box 180, 10002, Zagreb, Croatia

2. b Department of Chemistry , Faculty of Science, University of Zagreb , Horvatovac 102 a, 10002, Zagreb, Croatia

3. c MoD, Laboratory for NBC Protection , Ilica 256b, 10000, Zagreb, Croatia

4. d Department of Chemistry , University of New Orleans , New Orleans, LA, 70148, USA

Publisher

Informa UK Limited

Subject

General Chemistry

Link

https://www.tandfonline.com/doi/pdf/10.1080/10610270701268815

Reference34 articles.

1. Reactions of Diborane with Alkali Metal Hydrides and Their Addition Compounds. New Syntheses of Borohydrides. Sodium and Potassium Borohydrides1

2. The stereochemistry of cyclohexane derivatives

3. Asymmetric Induction in the Borohydride Reduction of Carbonyl Compounds by Means of a Chiral Phase-Transfer Catalyst

4. Boone , J. R. and Ashby , E. C. 1979. Topics in Stereoselectivity, Edited by: Eliel , E. L. and Allinger , N. L. vol. 11, 53New York: Interscience.

5. The Stereochemistry of Hydride Reductions

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