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Phosphorus, Sulfur, and Silicon and the Related Elements Volume 56, 1991 - Issue 1-4
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Original Articles

PHOSPHORUS-NITROGEN COMPOUNDS. PART 68.1 THE REACTIONS OF HEXACHLOROCYCLOTRIPHOSPHAZATRIENE ANDOCTACHLOROCYCLOTETRAPHOSPHAZATETRAENE WITH PENTAERYTHRITOL

Homaid A. Al-Madfa Department of Chemistry, Birkbeck College (University of London), Gordon House, Gordon Square, London, WCIH OPP, UK
,
Leylá S. Shaw Department of Chemistry, Birkbeck College (University of London), Gordon House, Gordon Square, London, WCIH OPP, UK
,
Née Gözen Department of Chemistry, Birkbeck College (University of London), Gordon House, Gordon Square, London, WCIH OPP, UK
&
Robert A. Shaw Department of Chemistry, Birkbeck College (University of London), Gordon House, Gordon Square, London, WCIH OPP, UK
Pages 133-142 | Received 02 May 1990, Published online: 23 Sep 2006

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Zhiyu Ju, Yong Ye, Le Wang, Xincheng Liao & Yufen Zhao. (2009) Synthesis and Characterization of Chloropentaaryloxycyclotriphosphazene Derivatives. Phosphorus, Sulfur, and Silicon and the Related Elements 184:8, pages 2103-2108.
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AbdullaH. Alkubaisi, SorabR. Contractor, HaroldG. Parkes, LeylaS. Shaw, Nŕe Gözen & RobertA. Shaw. (1991) PHOSPHORUS-NITROGEN COMPOUNDS. PART 69.1 THE REACTIONS OF GEMINAL TETRACHLORO-1′, 3′-PROPANEDIOXYCYCLOTRIPHOSPHAZA-TRIENE WITH PRIMARY AND SECONDARY AMINES. THE USE OF THE METHYLENE PROTONS OF THE 1′,3′-PROPANEDIOXY GROUP TO DISTINGUISH POSITIONAL AND GEOMETRIC ISOMERS. Phosphorus, Sulfur, and Silicon and the Related Elements 56:1-4, pages 143-156.
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Articles from other publishers (12)

Aylin Uslu & Serkan Yeşilot. (2015) Chiral configurations in cyclophosphazene chemistry. Coordination Chemistry Reviews 291, pages 28-67.
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Aylin Uslu, Simon J. Coles, David B. Davies, Mükremin Esen, Michael B. Hursthouse & Adem Kılıç. (2010) Effect of gem 2,2′-disubstitution and base in the formation of spiro- and ansa-1,3-propandioxy derivatives of cyclotriphosphazenes. Inorganica Chimica Acta 363:13, pages 3506-3515.
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Simon J. Coles, David B. Davies, Michael B. Hursthouse, Adem Kılıç, Şule Şahin, Robert A. Shaw & Aylin Uslu. (2007) Stereogenic properties of spiranes combined with one or two equivalent conventional centres of chirality. Journal of Organometallic Chemistry 692:13, pages 2811-2821.
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Simon J. Coles, David B. Davies, Robert J. Eaton, Michael B. Hursthouse, Adem Kılıç, Robert A. Shaw & Aylin Uslu. (2007) Stereogenic properties of spiranes combined with four equivalent conventional centres of chirality. Dalton Trans.:20, pages 2040-2047.
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Simon J. Coles, David B. Davies, Robert J. Eaton, Michael B. Hursthouse, Adem Kılıç, Robert A. Shaw & Aylin Uslu. (2006) The structural and stereogenic properties of pentaerythritoxy-bridged cyclotriphosphazene derivatives: spiro–spiro, spiro–ansa and ansa–ansa isomers. Dalton Trans.:10, pages 1302-1312.
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Aylin Uslu, Simon J. Coles, David B. Davies, Robert J. Eaton, Michael B. Hursthouse, Adem Kılıç & Robert A. Shaw. (2005) Stereoisomerism in Pentaerythritol‐Bridged Cyclotriphosphazene Tri‐Spiranes: Spiro and Ansa 1,3‐Propanediyldioxy Disubstituted Derivatives. European Journal of Inorganic Chemistry 2005:6, pages 1042-1047.
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Simon J. Coles, David B. Davies, Robert J. Eaton, Michael B. Hursthouse, Adem Kılıç, Robert A. Shaw & Aylin Uslu. (2004) Chiral Configurations of Spirane‐Bridged Cyclotriphosphazenes. European Journal of Organic Chemistry 2004:9, pages 1881-1886.
Crossref
John C. Tebby. 2001. Phosphorus-Carbon Heterocyclic Chemistry. Phosphorus-Carbon Heterocyclic Chemistry 671 705 .
. 1996. Comprehensive Heterocyclic Chemistry II. Comprehensive Heterocyclic Chemistry II 1169 1326 .
John C. Tebby. 1996. Comprehensive Heterocyclic Chemistry II. Comprehensive Heterocyclic Chemistry II 863 888 .
Christopher W. Allen. (1994) Linear, cyclic and polymeric phosphazenes. Coordination Chemistry Reviews 130:1-2, pages 137-173.
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H. A. AL‐MADFA, L. S. SHAW & R. A. SHAW. (2010) ChemInform Abstract: Phosphorus‐Nitrogen Compounds. Part 68. The Reactions of Hexachlorocyclotriphosphazatriene and Octachlorocyclotetraphosphazatetraene with Pentaerythritol.. ChemInform 22:21.
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