Preparation of ω-Hydroxy Acids by Reduction of α,ω-Methylene Diesters with NaBH4
Author:
Publisher
Informa UK Limited
Subject
Organic Chemistry
Link
http://www.tandfonline.com/doi/pdf/10.1080/00397919708004080
Reference13 articles.
1. Fieser, L. F. and Fieser, M. 1967.Reagents for Organic Synthesis, Vol. 1, 1051New York: John Wiley & Sons.
2. Volume properties of some linear and ring oligomer solutions
3. On the preparation of bilirubins of the natural ? series substituted with a propionic acid residue and a hydroxypropyl group
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1. Solvent-free synthesis of symmetric methylene diesters via direct reaction of aromatic carboxylates with 1,n-dihaloalkanes;RSC Advances;2021
2. Synthesis of the symmetrical methylene diesters from carboxylic ionic liquids;Canadian Journal of Chemistry;2017-07
3. ChemInform Abstract: Preparation of ω-Hydroxy Acids by Reduction of α,ω- Methylene Diesters with NaBH4.;ChemInform;2010-08-03
4. Solution Structure of Mesobiliverdin XIIIα Bridged Between the Propionic Acid Substituents [1];Monatshefte für Chemie / Chemical Monthly;1998-05
5. Zur Struktur des über die Propionsäurereste überbrückten Mesobilirubin XIIIα in Lösung;Monatshefte fuer Chemie/Chemical Monthly;1998
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