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Phosphorus, Sulfur, and Silicon and the Related Elements Volume 47, 1990 - Issue 1-2
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Original Articles

ORGANIC PHOSPHORUS COMPOUNDS 881 SULFONIC- AND SULFINIC ACID ANALOGUES OF GLYPHOSATE

Ludwig Maier CIBA-GEIGY AG, Agrochemicals Division, CH-4002, Basel, Switzerland
Pages 43-46 | Received 25 Apr 1989, Published online: 04 Oct 2006

Citations (6)

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Read on this site (1)

Ludwig Maier. (1999) What are the Requirements in the Glyphosate Molecule in Order to be Herbicidally Active?. Phosphorus, Sulfur, and Silicon and the Related Elements 144:1, pages 429-432.
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Articles from other publishers (5)

Kandula Madhu Kumar Reddy, Shaik Mahammad Sadik, Nagaripati Saichaithanya, Kotha Peddanna, Nemallapudi Bakthavatchala Reddy, Gundala Sravya, Zyryanov Grigory V & Cirandur Suresh Reddy. (2017) One-pot green synthesis and cytotoxicity of new α-aminophosphonates. Research on Chemical Intermediates 43:12, pages 7087-7103.
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Shamrao T. Disale, Sandip R. Kale, Sandeep S. Kahandal, Thandankorai G. Srinivasan & Radha V. Jayaram. (2012) Choline chloride·2ZnCl2 ionic liquid: an efficient and reusable catalyst for the solvent free Kabachnik–Fields reaction. Tetrahedron Letters 53:18, pages 2277-2279.
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Ludwig Maier. (2000) What are the requirements in the glyphosate molecule in order for it to be herbicidally active?. Heteroatom Chemistry 11:7, pages 454-469.
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Michel Mulliez & Carole Naudy. (1994) Synthése de Sels d'α-aminoacides sulfiniques substitués á lázote par un groupe méthane- ou p-toluéne-sulfonyle. Tetrahedron 50:18, pages 5401-5412.
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L. MAIER. (1990) ChemInform Abstract: Organic Phosphorus Compounds. Part 88. Sulfonic and Sulfinic Acid Analogues of Glyphosate.. ChemInform 21:37.
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