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Synthetic Communications
An International Journal for Rapid Communication of Synthetic Organic Chemistry
Volume 26, 1996 - Issue 1
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Original Articles

Concise Approach to 1-thiaHydantocidin

Clemens Lamberth SANDOZ AGRO Ltd., Chemical Research, CH-4002 Basel, Switzerland
&
Stefan Blarer SANDOZ AGRO Ltd., Chemical Research, CH-4002 Basel, Switzerland
Pages 75-81 | Received 15 May 1995, Published online: 21 Aug 2006

Citations (19)

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StewartK. Richardson, AmyR. Howell & Rosa Taboada. (2006) SYNTHESIS AND PROPERTIES OF PSICO-NUCLEOSIDES. Organic Preparations and Procedures International 38:2, pages 101-176.
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Clemens Lamberth. (2004) Sulfur chemistry in crop protection . Journal of Sulfur Chemistry 25:1, pages 39-62.
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Articles from other publishers (17)

Ian J. Rosenstein. 2004. Organic Reactions. Organic Reactions 1 654 .
Clemens Lamberth. 2019. Imides. Imides 335 352 .
Martín Soto, Humberto Rodríguez-Solla & Raquel Soengas. 2019. Carbohydrate-spiro-heterocycles. Carbohydrate-spiro-heterocycles 171 213 .
Raquel Soengas, Gustavo da Silva & Juan Estévez. (2017) Synthesis of Spironucleosides: Past and Future Perspectives. Molecules 22:11, pages 2028.
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Katalin Czifrák, András Páhi, Szabina Deák, Attila Kiss-Szikszai, Katalin E. Kövér, Tibor Docsa, Pál Gergely, Kyra-Melinda Alexacou, Maria Papakonstantinou, Demetres D. Leonidas, Spyros E. Zographos, Evangelia D. Chrysina & László Somsák. (2014) Glucopyranosylidene-spiro-iminothiazolidinone, a new bicyclic ring system: Synthesis, derivatization, and evaluation for inhibition of glycogen phosphorylase by enzyme kinetic and crystallographic methods. Bioorganic & Medicinal Chemistry 22:15, pages 4028-4041.
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Inés Pérez-Martín & Ernesto Suárez. 2012. Encyclopedia of Radicals in Chemistry, Biology and Materials. Encyclopedia of Radicals in Chemistry, Biology and Materials.
Tien Q. Pham, Stephen G. Pyne, Brian W. Skelton & Allan H. White. (2005) Synthesis of Carbocyclic Hydantocidins via Regioselective and Diastereoselective Phosphine-Catalyzed [3 + 2]-Cycloadditions to 5-Methylenehydantoins. The Journal of Organic Chemistry 70:16, pages 6369-6377.
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Clemens Lamberth. (2005) Nucleoside Chemistry in Crop Protection. HETEROCYCLES 65:3, pages 667.
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N.W.A. Geraghty. 2005. Comprehensive Organic Functional Group Transformations II. Comprehensive Organic Functional Group Transformations II 27 128 .
Jean-Pierre Praly, Guo-Rong Chen, Joëlle Gola & Georg Hetzer. (2000) Stereocontrolled Access to Higher Sugars (Non-1-en-4-ulopyranosyl Derivatives) and Glycomimetics [3-(β-D-Glycopyranosyl)-1-propenes and(3Z)-4,8-Anhydro-nona-1,3-dienitols]. European Journal of Organic Chemistry 2000:16, pages 2831-2838.
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Annabelle Renard, Mitsuharu Kotera, Marie-Christine Brochier & Jean Lhomme. (2000) Deoxyhydantocidin: Synthesis by Base-Catalyzed Spiro Cyclization and Interconversion with the 1′-Epimer. European Journal of Organic Chemistry 2000:9, pages 1831-1840.
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Leo A. Paquette, Stephen Brand & Carsten Behrens. (1999) An Enantioselective Ring Expansion Route Leading to Furanose and Pyranose Nucleosides Featuring Spirodiketopiperazines at the Anomeric Position. The Journal of Organic Chemistry 64:6, pages 2010-2025.
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Erzsébet Ősz, László Szilágyi, László Somsák & Attila Bényei. (1999) Syntheses of novel glycosylidene-spiro-heterocycles related to hydantocidin. Tetrahedron 55:8, pages 2419-2430.
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. (1998) Joint European IIS Conference. Central European division and UK chapter. Journal of Labelled Compounds and Radiopharmaceuticals 41:11, pages 1017-1082.
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Erzsébet Õsz, Erzsébet Sós, László Somsák, László Szilágyi & Zoltán Dinya. (1997) A straightforward route to hydantocidin analogues with pyranose ring structure. Tetrahedron 53:16, pages 5813-5824.
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Tilmann W. Brandstetter, Carmen de la Fuente, Yong-ha Kim, Louise N. Johnson, Sarah Crook, Paul M.de Q. Lilley, David J. Watkin, Katerina E. Tsitsanou, Spyros E. Zographos, Enangelia D. Chrysina, Nikos G. Oikonomakos & George W.J. Fleet. (1996) Glucofuranose analogues of hydantocidin. Tetrahedron 52:32, pages 10721-10736.
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C. LAMBERTH & S. BLARER. (2010) ChemInform Abstract: Concise Approach to 1‐Thiahydantocidin.. ChemInform 27:22.
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