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Phosphorus, Sulfur, and Silicon and the Related Elements Volume 48, 1990 - Issue 1-4
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Original Articles

1,2-DIHYDROXY-ETHANE-1,2-DIPHOSPHONIC ACID DERIVATIVES: STEREOCHEMICAL INVESTIGATIONS BY NMR METHODS

Martin Murray Department of Organic Chemistry, University of Bristol, Cantock's Close, Bristol, BS8 ITS, England
,
Kevin M. Higgins Department of Organic Chemistry, University of Bristol, Cantock's Close, Bristol, BS8 ITS, England
,
Gerhard Hägele Institut für Anorganische Chemie und Strukturchemie I, Universität Düsseldorf, Universitätsstraße 1, D-4000, Düsseldorf, F. R. G.
,
Angelika Gaedcke Institut für Anorganische Chemie und Strukturchemie I, Universität Düsseldorf, Universitätsstraße 1, D-4000, Düsseldorf, F. R. G.
&
John Mikroyannidis Department of Chemistry, University of Patras, Greece
Pages 117-130 | Received 04 Sep 1989, Published online: 04 Oct 2006

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Gerhard Hägele, Joachim Dettmann, Krzysztof Huben, Stefan Jankowski, Erika Bálint & György Keglevich. (2014) 2,3-Bisphosphonosuccinic Acid Hexamethyl Ester [(CH3O)2(O)P-CH-COOCH3]2 – NMR-Spectroscopic Studies of ABX and [AM3R3X]2+Z6 Spin Systems. Phosphorus, Sulfur, and Silicon and the Related Elements 189:9, pages 1315-1327.
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Articles from other publishers (4)

Levon L. Khemchyan, Julia V. Ivanova, Sergey S. Zalesskiy, Valentine P. Ananikov, Irina P. Beletskaya & Zoya A. Starikova. (2014) Unprecedented Control of Selectivity in Nickel‐Catalyzed Hydrophosphorylation of Alkynes: Efficient Route to Mono‐ and Bisphosphonates. Advanced Synthesis & Catalysis 356:4, pages 771-780.
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Yu. V. Ivanova, L. L. Khemchyan, S. S. Zalesskii, V. P. Ananikov & I. P. Beletskaya. (2013) Synthesis of alkyl tetraphosphonates: First example of nickel catalyst for H-phosphonates addition to diynes. Russian Journal of Organic Chemistry 49:8, pages 1099-1107.
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Zvi RappoportR. S. Edmundson. 2010. Patai's Chemistry of Functional Groups. Patai's Chemistry of Functional Groups.
Zvi RappoportR. S. Edmundson. 2010. Patai's Chemistry of Functional Groups. Patai's Chemistry of Functional Groups.

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