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Corriu, R. J. P., Lanneau, G. F., Leclercq, D. (1983) Exocyclic Substitution of Five-Membered Ring Chlorophosphates: A Reexamination of the rule For Nucleophilic Substitution at Phosphorus. Phosphorus and Sulfur and the Related Elements, 18. 197-200 doi:10.1080/03086648308076000

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Reference TypeJournal (article/letter/editorial)
TitleExocyclic Substitution of Five-Membered Ring Chlorophosphates: A Reexamination of the rule For Nucleophilic Substitution at Phosphorus
JournalPhosphorus and Sulfur and the Related Elements
AuthorsCorriu, R. J. P.Author
Lanneau, G. F.Author
Leclercq, D.Author
Year1983 (December)Volume18
PublisherInforma UK Limited
DOIdoi:10.1080/03086648308076000Search in ResearchGate
Generate Citation Formats
Mindat Ref. ID9772810Long-form Identifiermindat:1:5:9772810:0
GUID0
Full ReferenceCorriu, R. J. P., Lanneau, G. F., Leclercq, D. (1983) Exocyclic Substitution of Five-Membered Ring Chlorophosphates: A Reexamination of the rule For Nucleophilic Substitution at Phosphorus. Phosphorus and Sulfur and the Related Elements, 18. 197-200 doi:10.1080/03086648308076000
Plain TextCorriu, R. J. P., Lanneau, G. F., Leclercq, D. (1983) Exocyclic Substitution of Five-Membered Ring Chlorophosphates: A Reexamination of the rule For Nucleophilic Substitution at Phosphorus. Phosphorus and Sulfur and the Related Elements, 18. 197-200 doi:10.1080/03086648308076000
In(n.d.) Phosphorus and Sulfur and the Related Elements Vol. 18. Informa UK Limited

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Corriu, R., Daffi, A., Lanneau, G. (1987) Catalyzed Methanolysis of Five Membered Ring Phosphoenolates. Phosphorus and Sulfur and the Related Elements, 30. 784 doi:10.1080/03086648708079276
Corriu, R. J. P., Lanneau, G. F., Leclercq, D. (1980) NUCLEOPHILIC ASSISTANCE IN THE FORMATION OF PYROPHOSPHONATE: EFFECTIVE SIDE-REACTION OF HALOGENOPHOSPHORUS COMPOUNDS WITH WATER IN APROTIC SOLVENTS. Phosphorus and Sulfur and the Related Elements, 9. 149-154 doi:10.1080/03086648008078233
Dahl, Otto (1983) Mechanism of Nucleophilic Substitution at Tricovalent Phosphorus. Phosphorus and Sulfur and the Related Elements, 18. 201-204 doi:10.1080/03086648308076001
CORRIU, R. J. P., DUTHEIL, J.-P., LANNEAU, G. F. (1984) ChemInform Abstract: SILICON PHOSPHORUS ANALOGIES. FLUORIDE ACTIVATION OF NUCLEOPHILIC DISPLACEMENT AT THE TETRAHEDRAL PHOSPHORUS: AN EXAMPLE OF NUCLEOPHILIC ASSISTANCE T NUCLEOPHILIC SUBSTITUTION. 3. Chemischer Informationsdienst, 15 (21) doi:10.1002/chin.198421256
Lanneau, Gérard F. (1986) SILICON-PHOSPHORUS ANALOGIES THE MECHANISM OF NUCLEOPHILIC SUBSTITUTION AT SILICON AND PHOSPHORUS ACTIVATED BY EXTERNAL NUCLEOPHILES EXTENSION OF COORDINATION OF THE REACTIVE SPECIES. Phosphorous and Sulfur and the Related Elements, 27. 43-54 doi:10.1080/03086648608072757
King, J. F., Guo, Z. R., Lock, J. D. (1994) THE EFFECT OF LOCATING THE SULFONYL GROUP IN A FIVE-MEMBERED RING ON THE BALANCE OF ELIMINATION VS. SUBSTITUTION REACTIONS OF SULFONIC ACID DERIVATIVES. Phosphorus, Sulfur, and Silicon and the Related Elements, 97. 191-197 doi:10.1080/10426509408020742
Okuyama, Tadashi (1994) Mechanisms of Nucleophilic Substitution at Sulfur. Phosphorus, Sulfur, and Silicon and the Related Elements, 95. 113-125 doi:10.1080/10426509408034205
Kolodiazhnyi, Oleg I. (2019) Stereochemistry of electrophilic and nucleophilic substitution at phosphorus. Phosphorus, Sulfur, and Silicon and the Related Elements, 194. 396-400 doi:10.1080/10426507.2018.1521409
Holmes, Robert R. (1995) THE STEREOCHEMISTRY OF NUCLEOPHILIC SUBSTITUTION AT TETRACOORDINATED SILICON. Phosphorus, Sulfur, and Silicon and the Related Elements, 99. 207-238 doi:10.1080/10426509508031346
Corriu, R. J. P. (1986) NUCLEOPHILIC SUBSTITUTIONS AT SILICON AND PHOSPHORUS. A COMPARISON OF CONTROLLING FACTORS. Phosphorous and Sulfur and the Related Elements, 27. 1-12 doi:10.1080/03086648608072754
Corriu, Robert J. P., Dutheil, Jean Pierre, Lanneau, Gerard F. (1984) Silicon phosphorus analogies. Fluoride activation of nucleophilic displacement at the tetrahedral phosphorus: an example of nucleophilic assistance to nucleophilic substitution. 3. Journal Of The American Chemical Society, 106 (4) 1060-1065 doi:10.1021/ja00316a041
 
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