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Synthetic Communications
An International Journal for Rapid Communication of Synthetic Organic Chemistry
Volume 25, 1995 - Issue 22
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Original Articles

New Reagents for the Reductive Quenching of Ozonolysis Reactions

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Pages 3589-3595 | Received 11 Apr 1995, Published online: 23 Sep 2006

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Thomas J. Fisher & Patrick H. Dussault. (2017) Alkene ozonolysis. Tetrahedron 73:30, pages 4233-4258.
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Jan Hendrik Wübbeler, Sebastian Hiessl, Christina Meinert, Anja Poehlein, Jörg Schuldes, Rolf Daniel & Alexander Steinbüchel. (2015) The genome of Variovorax paradoxus strain TBEA6 provides new understandings for the catabolism of 3,3′-thiodipropionic acid and hence the production of polythioesters. Journal of Biotechnology 209, pages 85-95.
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Barbara Satola, Jan Hendrik Wübbeler & Alexander Steinbüchel. (2012) Metabolic characteristics of the species Variovorax paradoxus. Applied Microbiology and Biotechnology 97:2, pages 541-560.
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Jan Hendrik Wübbeler, Nadine Bruland, Milena Wozniczka & Alexander Steinbüchel. (2010) Biodegradation of the xenobiotic organic disulphide 4,4′-dithiodibutyric acid by Rhodococcus erythropolis strain MI2 and comparison with the microbial utilization of 3,3′-dithiodipropionic acid and 3,3′-thiodipropionic acid. Microbiology 156:4, pages 1221-1233.
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N. Bruland, S. Bathe, A. Willems & A. Steinbuchel. (2009) Pseudorhodoferax soli gen. nov., sp. nov. and Pseudorhodoferax caeni sp. nov., two members of the class Betaproteobacteria belonging to the family Comamonadaceae. INTERNATIONAL JOURNAL OF SYSTEMATIC AND EVOLUTIONARY MICROBIOLOGY 59:11, pages 2702-2707.
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Slavcho Rakovsky, Metody Anachkov & Gennady Zaikov. (2009) Fields of Ozone Applications. Chemistry & Chemical Technology 3:2, pages 139-161.
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Nadine Bruland, Jan Hendrik Wu¨bbeler & Alexander Steinbu¨chel. (2009) 3-Mercaptopropionate Dioxygenase, a Cysteine Dioxygenase Homologue, Catalyzes the Initial Step of 3-Mercaptopropionate Catabolism in the 3,3-Thiodipropionic Acid-degrading Bacterium Variovorax paradoxus. Journal of Biological Chemistry 284:1, pages 660-672.
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G.E. Zaikov, S. Rakovsky & M. Anachkov. 2000. Kirk-Othmer Encyclopedia of Chemical Technology. Kirk-Othmer Encyclopedia of Chemical Technology.
Richard A. Berglund & Matthew M. Kreilein. 2001. Encyclopedia of Reagents for Organic Synthesis. Encyclopedia of Reagents for Organic Synthesis.
Yung-Son Hon & Kun-Chan Wu. (2003) Polymer-supported tertiary amine in organic synthesis: a useful reagent in the conversion of alkenes to carbonyl compounds via the corresponding ozonides. Tetrahedron 59:4, pages 493-498.
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Sarbajit Banerjee & Stanislaus S. Wong. (2002) Rational Sidewall Functionalization and Purification of Single-Walled Carbon Nanotubes by Solution-Phase Ozonolysis. The Journal of Physical Chemistry B 106:47, pages 12144-12151.
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Madeline B. Graham & H. P. Tyman. (2002) Ozonization of phenols from Anacardium occidentale (cashew) . Journal of the American Oil Chemists' Society 79:7, pages 725-732.
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Andreas Kirschning, Holger Monenschein & Rüdiger Wittenberg. (2001) Functionalized Polymers-Emerging Versatile Tools for Solution-Phase Chemistry and Automated Parallel Synthesis. Angewandte Chemie International Edition 40:4, pages 650-679.
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Andreas Kirschning, Holger Monenschein & Rüdiger Wittenberg. (2001) Funktionalisierte Polymere - zukunftsträchtige Werkzeuge für die Chemie in Lösung und die automatisierte Parallelsynthese. Angewandte Chemie 113:4, pages 670-701.
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Jozef Kula. (1999) Safer ozonolysis reactions: A compilation of laboratory experience. Chemical Health & Safety 6:6, pages 21-22.
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David H. Drewry, Diane M. Coe & Steve Poon. (1999) Solid-supported reagents in organic synthesis. Medicinal Research Reviews 19:2, pages 97-148.
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S. Rimmer & J. R. Ebdon. (1996) On the effect of the use of dimethylacetamide as solvent on the work-up of polymer ozonides with polymer-supported reagents. Journal of Polymer Science Part A: Polymer Chemistry 34:17, pages 3591-3593.
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R. B. APPELL, I. A. TOMLINSON & I. HILL. (2010) ChemInform Abstract: New Reagents for the Reductive Quenching of Ozonolysis Reactions.. ChemInform 27:6.
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