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Current Organic Chemistry

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ISSN (Print): 1385-2728
ISSN (Online): 1875-5348

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Erratum

Newer Developments in the Synthesis of P-Heterocycles

Author(s):

Volume 23, Issue 19, 2019

Page: [2141 - 2141] Pages: 1

DOI: 10.2174/138527282319191219122010

Abstract

Due to an overlook the reference nos. 1, 6, 8, 15, 16, 34, 40, 41, 46, 47, 48, 68, 74, 80, 81 & 96 were published erroneously in the article, entitled: “Newer Developments in the Synthesis of P-Heterocycles” in “Current Organic Chemistry”, 2019, Vol. 23, No. 12, pp. 1342- 1355.”

Erratum For:
Newer Developments in the Synthesis of P-Heterocycles

« Previous
[1]
Keglevich, G. Application of Microwave Irradiation in the Synthesis of P-Heterocycles.In: Green Synthetic Approaches for Biologically Relevant Heterocycles; Brahmachari, G., Ed.; Elsevier: Amsterdam, 2015, pp. 559-570.
[http://dx.doi.org/10.1016/B978-0-12-800070-0.00020-7]
[6]
Keglevich, G.; Bálint, E.; Kiss, N.Z. The Use of MW in Organophosphorus Chemistry.In: Milestones in Microwave Chemistry – SpringerBriefs in Molecular Science; Keglevich, G., Ed.; Springer: Switzerland, 2016, pp. 47-76.
[http://dx.doi.org/10.1007/978-3-319-30632-2_3]
[8]
Keglevich, G.; Kiss, N.Z.; Bálint, E.; Bagi, P.; Grün, A.; Kovács, T.; Henyecz, R.; Ábrányi-Balogh, P. Milestones in Microwave-assisted Organophosphorus Chemistry. Phosphorus Sulfur Silicon Relat. Elem, 2016, 191, SI, 1416-1420.
[http://dx.doi.org/10.1080/10426507.2016.1211657]
[15]
Minami, T.; Okauchi, T. Vinyl- and Arylphosphorus Derivatives.In: Comprehensive Organic Functional Group Transformations II; Katritzky, A.R.; Taylor, R.J.K., Eds.; Elsevier: Oxford, 2005, pp. 853-907.
[http://dx.doi.org/10.1016/B0-08-044655-8/00038-6]
[16]
Cristau, H-J.; Virieux, D. Product Class 40: Arylphosphinic Acids and Derivatives In: Science of Synthesis: Houben-Weyl Methods of Molecular Transformations, 1st ed.; Ramsden, C.A.; Bellus, D., Eds.; Georg Thieme Verlag: Stuttgart; 2007.Vol. 31b, p. 1963.
[http://dx.doi.org/10.1055/sos-SD-031-02233]
[34]
Keglevich, G.; Mucsi, Z. Interpretation of the Rate Enhancing Effect of Microwaves.In: Microwave Chemistry; Cravotto, G.; Carnaroglio, D., Eds.; De Gruyter: Berlin, 2017, pp. 53-64.
[http://dx.doi.org/10.1515/9783110479935-004]
[40]
Amitrano, R.; Koch, P.; Neuber, M.; Neumann, D.; Petrovic, P.; Roos, M.; Vedder, C. ALLESSAN CAP- A Highly Versatile and Affordable Coupling Agent In: Peptides for Youth: Advances in Experimental Medicine and Biology, Del Valle, S.; Escher, E.; Lubell, W.D., Eds.; Springer: New York. 2009, 611, pp. 193-194.
[41]
Schwarz, M. n-Propane Phosphonic Acid Anhydride - A Condensation Reagent. Synlett, 2000, 2000(9), 1369.
[46]
Henyecz, R.; Milen, M.; Kánai, K.; Keglevich, G. The Use of the T3P® Reagent in the Synthesis of Phosphinic and Phosphonic Derivatives.In: Organophosphorus Chemistry-Novel Developments; Keglevich, G., Ed.; De Gruyter: Berlin, 2018, pp. 148-157.
[http://dx.doi.org/10.1515/9783110535839-007]
[47]
Frank, A.W. Phosphorus Acids (Thio-, Seleno Analogs) and Derivatives.In: Organic Phosphorus Compounds; Kosolapoff, G.M.; Maier, L., Eds.; J. Wiley & Sons, Inc.: New York, 1972, Vol. 4, pp. 264-265.
[48]
Houben-Weyl, Methoden der organischen Chemie, Phosphor-Verbindungen II, Band E2, Regitz, M., Ed.; Georg Thieme Verlag: Stuttgart, 1982; pp. 142-143, pp. 310-313.
[68]
Kovács, T.; Keglevich, G. Deoxygenation of Phosphine Oxides.In: Organophosphorus Chemistry – Novel Developments; Keglevich, G., Ed.; De Gruyter: Berlin, 2018, pp. 179-198.
[http://dx.doi.org/10.1515/9783110535839-009]
[74]
Kovács, T.; Keglevich, G. The deoxygenation of phosphine oxides under green chemical conditions. Phosphorus Sulfur Silicon Relat. Elem., 2016, 191, 359-366.
[http://dx.doi.org/10.1080/10426507.2015.1065259]
[80]
O’Brien, C.J.; Nixon, Z.S.; Holohan, A.J.; Kunkel, S.R.; Tellez, J.L.; Doonan, B.J.; Coyle, E.E.; Lavigne, F.; Kang, L.J.; Przeworski, K.C.; Part, I. The development of the catalytic wittig reaction. Chem. Eur. J, 2013, 19(45), 15281-15289.
[http://dx.doi.org/10.1002/chem.201301444] [PMID: 24115040]
[81]
O’Brien, C.J.; Lavigne, F.; Coyle, E.E.; Holohan, A.J.; Doonan, B.J. Breaking the ring through a room temperature catalytic Wittig reaction. Chem. Eur. J, 2013, 19(19), 5854-5858.
[http://dx.doi.org/10.1002/chem.201300546] [PMID: 23526683]
[96]
O’Brien, C.J. Catalytic Wittig and Mitsunobu reactions. WO 2010118042, 2010; U.S. Patent US 8901365, 2014.

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