Pure and Applied Chemistry

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• Kajiyama Kazumasa, Fujimori Sayaka, Yasuoka Daisuke, Otsuka Takeshi, Miyamoto Takeshi Ken: Aroylspirophosphoranes bearing two naphth-1,8-diyl-8-oxy groups: synthesis, crystal structure, and np(Oapical)→π∗(CO) charge transfer interaction. Tetrahedron 2013, 69, 9155. <http://dx.doi.org/10.1016/j.tet.2013.08.004>
• Jiang Xin-Dong, Matsukawa Shiro, Kojima Satoshi, Yamamoto Yohsuke: Synthesis and Characterization of Antiapicophilic Arsoranes and Related Compounds. Inorg. Chem. 2012, 51, 10996. <http://dx.doi.org/10.1021/ic3014893>
• Marciano Daniele, Columbus Ishay, Elias Shlomi, Goldvaser Michael, Shoshanim Ofir, Ashkenazi Nissan, Zafrani Yossi: Role of the P–F Bond in Fluoride-Promoted Aqueous VX Hydrolysis: An Experimental and Theoretical Study. J. Org. Chem. 2012, 77, 10042. <http://dx.doi.org/10.1021/jo301549z>
• Kojima Satoshi, Nakamoto Masaaki, Matsukawa Shiro, Akiba Kin-ya: Stereomutation of a diastereomeric pair of 10-P-5 hydroxyphosphoranes. Heteroatom Chem 2011, 22, 491. <http://dx.doi.org/10.1002/hc.20712>
• Koole Leo H., Olders Edith A. T. A., Opresnik Marko, Buck Henk M.: A kinetic study of the alkaline hydrolysis of four-coordinated phosphorus (PIV) compounds. Impact of conformational transmission in the transiently formed five-coordinated (PV-TBP) intermediates on reaction rate and product distribution. Recl Trav Chim Pays-Bas 2010, 109, 55. <http://dx.doi.org/10.1002/recl.19901090205>
• Yamamoto Yohsuke, Jiang Xin-Dong: Synthesis, structure, and reaction of tricoordinate stibine and tetracoordinate stiboranide. J Organomet Chem 2010, 695, 740. <http://dx.doi.org/10.1016/j.jorganchem.2009.12.009>
• López-Cortina Susana, Medina-Arreguin Araceli, Hernández-Fernández Eugenio, Bernès Sylvain, Guerrero-Alvarez Jorge, Ordoñez Mario, Fernández-Zertuche Mario: Stereochemistry of base-induced cleavage of methoxide ion on cis- and trans-1,4-diphenylphosphorinanium salts. A different behavior with a phenyl substituent. Tetrahedron 2010, 66, 6188. <http://dx.doi.org/10.1016/j.tet.2010.05.095>
• Matsukawa Shiro, Kakuda Ken-ichiro, Jiang Xin-Dong, Fukuzaki Yuta, Zhao Wei-Li, Li Lin-Song, Shen Huai-Bin, Kojima Satoshi, Yamamoto Yohsuke: Efficient synthesis of tetradecafluoro-4-phenylheptan-4-ol by a Cannizzaro-type reaction and application of the alcohol as a bulky Martin ligand variant for a new anti-apicophilic phosphorane. Dalton Trans 2010, 39, 9823. <http://dx.doi.org/10.1039/c0dt00539h>
• Jiang Xin-Dong, Matsukawa Shiro, Yamamichi Hideaki, Kakuda Ken-ichiro, Kojima Satoshi, Yamamoto Yohsuke: Stereomutation and Experimental Determination of the Relative Stability of DiastereomericO-Equatorial Anti-Apicophilic Spirophosphoranes. Eur J Org Chem 2008, 2008, 1392. <http://dx.doi.org/10.1002/ejoc.200700971>
• Jiang Xin-Dong, Matsukawa Shiro, Yamamoto Yohsuke: Synthesis, structure and isomerization of arylphosphoranes with anti-apicophilic bonding modes using a novel bidentate ligand with two C2F5 groups. Dalton Trans 2008, 3678. <http://dx.doi.org/10.1039/b802947d>
• Jiang Xin-Dong, Kakuda Ken-ichiro, Matsukawa Shiro, Yamamichi Hideaki, Kojima Satoshi, Yamamoto Yohsuke: Synthesis and Application of a Bidentate Ligand Based on Decafluoro-3-phenyl-3-pentanol: Steric Effect of Pentafluoroethyl Groups on the Stereomutation of O-Equatorial C-Apical Spirophosphoranes. Chem Asian J 2007, 2, 314. <http://dx.doi.org/10.1002/asia.200600334>
• Stöckli Markus J., Rüedi Peter: Synthesis of Enantiomerically Pure 1,5,5-Trideuteratedcis- andtrans-2,4-Dioxa-3-phosphadecalins.31P-NMR Evidence of Covalent-Bond Formation and the Stereochemical Implications in the Course of the Inhibition ofδ-Chymotrypsin. HCA 2007, 90, 2058. <http://dx.doi.org/10.1002/hlca.200790215>
• Kajiyama Kazumasa, Yoshimune Miki, Kojima Satoshi, Akiba Kin-ya: A New Method for the Formation of Anti-apicophilic (O-cis) Spirophosphoranes – Kinetic Studies on the Stereomutation ofO-cis Arylspirophosphoranes to TheirO-trans Isomers. Eur J Org Chem 2006, 2006, 2739. <http://dx.doi.org/10.1002/ejoc.200600031>
• Tzokov Svetomir B., Momtcheva Rositza T., Petkov Dimiter D.: PHOSPHONYLATION BY A SPIROPHOSPHORANE: APPLICATION OF THE RIBOZYME CHEMISTRY IN THE BIOORGANIC SYNTHESIS. Phosphorus Sulfur Silicon Relat Elem 2004, 179, 1095. <http://dx.doi.org/10.1080/10426500490459713>
• Lee Ikchoon: Natural bond orbital analysis of the intrinsic reaction barriers in nucleophilic displacements. Int Rev Phys Chem 2003, 22, 263. <http://dx.doi.org/10.1080/0144235031000086058>
• Nakamoto Masaaki, Kojima Satoshi, Matsukawa Shiro, Yamamoto Yohsuke, Akiba Kin-ya: Stereomutation and apicophilicity of diastereomeric spirophosphoranes (10-P-5). J Organomet Chem 2002, 643-644, 441. <http://dx.doi.org/10.1016/S0022-328X(01)01440-1>
• Okuyama Tadashi, Sato Koichi, Ochiai Masahito: Reactions of 2,2-Dialkylvinyl Iodonium Salt with Halide Ions. Bull Chem Soc Jpn 2000, 73, 2341. <http://dx.doi.org/10.1246/bcsj.73.2341>
• Legrand Olivier, Brunel Jean Michel, Buono Gérard: Stereospezifische Wanderung eines P-Atoms von einem N- zu einem Csp2-Zentrum: Ringerweiterung chiraler Diazaphospholidinoxide. Angew Chem 1999, 111, 1574. <http://dx.doi.org/10.1002/(SICI)1521-3757(19990517)111:10<1574::AID-ANGE1574>3.0.CO;2-I>
• Okuyama Tadashi, Yamataka Hiroshi: A theoretical study on the reactivity of vinyl iodonium ions. Can J Chem 1999, 77, 577. <http://dx.doi.org/10.1139/v99-024>
• Furegati Stefan, Ganci Walter, Przibille Georg, Rüedi Peter: Stereochemistry of the Inhibition of δ-Chymotrypsin with Optically Activecis-Decaline-Type Organophosphates:31P-NMR studies. HCA 1998, 81, 1127. <http://dx.doi.org/10.1002/hlca.19980810526>
• Okuyama Tadashi, Takino Tomoki, Sato Koichi, Oshima Kunio, Imamura Shohei, Yamataka Hiroshi, Asano Tsutomu, Ochiai Masahito: Vinylic SN2 Reaction of 1-Decenyliodonium Salt with Halide Ions. Bull Chem Soc Jpn 1998, 71, 243. <http://dx.doi.org/10.1246/bcsj.71.243>
• Ganci Walter, Meier Eric J. M., Merckling Franco A., Przibille Georg, Ringeisen Urs, Rüedi Peter: Stereochemistry of the Inhibition of δ-Chymotrypsin with Optically Active Bicyclic Organophosphates:31P-NMR studies. HCA 1997, 80, 421. <http://dx.doi.org/10.1002/hlca.19970800208>
• Deiters Joan A., Holmes Robert R.: AB INITIO TREATMENT OF A PHOSPHORUS COORDINATE, TRIGONAL BIPYRAMIDAL TO PENTAFLUORIDE-PYRIDINE REACTION SQUARE PYRAMIDAL TO OCTAHEDRAL. Phosphorus Sulfur Silicon Relat Elem 1997, 123, 329. <http://dx.doi.org/10.1080/10426509708044220>
• Blachnik Roger, Hackmann Kerstin, Tattershall Bruce W.: Amino and μ-IMINO tetraphosphorus trisulfide compounds: NMR evidence for invertomers and bridged cages with an α- or β-P4S3 skeleton. J Polyhedron 1996, 15, 1415. <http://dx.doi.org/10.1016/0277-5387(95)00414-9>
• Huang Yande, Arif Atta M., Bentrude Wesley G.: X-RAY CRYSTALLOGRAPHIC STUDY OF PHOSPHORANES. EFFECTS ON EQUATORIAL O–P–O BOND ANGLES OF INCLUSION OF PHOSPHORUS IN A 1,3,2-DIOXAPHOSPHORINANE RING. Phosphorus Sulfur Silicon Relat Elem 1995, 103, 225. <http://dx.doi.org/10.1080/10426509508027381>
• Deiters Joan A., Holmes Robert R., Holmes Joan M.: FLUORINE AND CHLORINE APICOPHILICITIES IN FIVE-COORDINATED PHOSPHORUS AND SILICON COMPOUNDS VIA MOLECULAR ORBITAL CALCULATIONS. A MODEL FOR NUCLEOPHILIC SUBSTITUTION. Phosphorus Sulfur Silicon Relat Elem 1995, 99, 101. <http://dx.doi.org/10.1080/10426509508031340>
• Holmes Robert R.: THE STEREOCHEMISTRY OF NUCLEOPHILIC SUBSTITUTION AT TETRACOORDINATED SILICON. Phosphorus Sulfur Silicon Relat Elem 1995, 99, 207. <http://dx.doi.org/10.1080/10426509508031346>
• Kumara Swamy K. C., Holmes Joan M., Day Roberta O., Holmes Robert R.: FIRST STRUCTURAL STUDY OF A THIOPHOSPHORANE CONTAINING A SIX-MEMBERED RING. PHOSPHORUS-SULFUR VS PHOSPHORUS-OXYGEN LIGAND PREFERENCES. Phosphorus Sulfur Silicon Relat Elem 1995, 99, 257. <http://dx.doi.org/10.1080/10426509508031348>
• Swamy K. C. Kumara, Day Roberta O., Holmes Joan M., Holmes Robert R.: CONFORMATIONAL PREFERENCES OF SPIROCYCLIC PENTAOXYPHOSPHORANES VARYING IN RING SIZE. Phosphorus Sulfur Silicon Relat Elem 1995, 100, 1. <http://dx.doi.org/10.1080/10426509508037698>
• Burton Sarah D., Swamy K. C. Kumara, Holmes Joan M., Day Roberta O., Holmes Robert R.: CONFORMATIONAL PREFERENCES OF MONOCYCLIC PENTAOXYPHOSPHORANES VARYING IN RING SIZE. Phosphorus Sulfur Silicon Relat Elem 1995, 100, 23. <http://dx.doi.org/10.1080/10426509508037699>
• Swamy K. C. Kumara, Burton Sarah D., Holmes Joan M., Day Roberta O., Holmes Robert R.: CYCLIC OXYPHOSPHORANES. Phosphorus Sulfur Silicon Relat Elem 1995, 100, 67. <http://dx.doi.org/10.1080/10426509508037701>
• Day Roberta O., Sreelatha Channareddy, Deiters Joan A., Johnson Stephen E., Holmes Joan M., Howe Lori, Holmes Robert R.: ANIONIC FIVE-COORDINATED CYCLIC ORGANOFLUOROSILICATES VARYING IN RING SIZE FROM FIVE- TO SEVEN-MEMBERED. Phosphorus Sulfur Silicon Relat Elem 1995, 100, 87. <http://dx.doi.org/10.1080/10426509508037702>
• Prakasha T. K., Day Roberta O., Holmes Robert R.: DIEQUATORIAL AND AXIAL-EQUATORIAL ORIENTATIONS OF EIGHT-MEMBERED RINGS IN MONOCYCLIC PENTAOXYPHOSPHORANES CONTAINING TRIFLUOROETHOXY GROUPS. Phosphorus Sulfur Silicon Relat Elem 1995, 100, 129. <http://dx.doi.org/10.1080/10426509508037705>
• Holmes Robert R., Deiters Joan A.: CYCLIC PENTAOXYPHOSPHORANES AS MODELS FOR cAMP ACTION. AN AB INITIO APPROACH. Phosphorus Sulfur Silicon Relat Elem 1995, 100, 185. <http://dx.doi.org/10.1080/10426509508037708>
• Janzen Alexander F.: Ligand exchange and reaction mechanisms offluorinated compounds. Coord Chem Rev - 1994, 130, 355. <http://dx.doi.org/10.1016/0010-8545(94)80009-X>
• Lee Ikchoon, Kyung Kim Chan, Lee Bon-Su, Ha Tae-Kyu: Theoretical studies on the reaction of phosphoranes with anions. Journal of Molecular Structure: THEOCHEM 1993, 279, 191. <http://dx.doi.org/10.1016/0166-1280(93)90066-K>
• Yu Jaehoon, Sopchik Alan E., Arif Atta M., Bentrude Wesley G., Roeschenthaler G.-V.: Conformational properties of cyclic pentaalkoxy phosphoranes: Apical-equatorial attachment and nonchair conformation of the phosphorus-containing six-membered ring. Heteroatom Chem 1991, 2, 177. <http://dx.doi.org/10.1002/hc.520020120>
• Corriu Robert J.P., Kpoton Agapit, Poirier Monique, Royo Gérard, de Saxcé Arnaud, Colin Young J.: Pentacoordinated silicon compounds. Intramolecular ring closure, site preferences of substituents and the stability of the resulting chelates. J Organomet Chem 1990, 395, 1. <http://dx.doi.org/10.1016/0022-328X(90)85258-Z>
• Kumara Swamy K. C., Burton Sarah D., Holmes Joan M., Day Roberta O., Holmes Robert R.: CYCLIC OXYPHOSPHORANES. Phosphorus Sulfur Silicon Relat Elem 1990, 53, 437. <http://dx.doi.org/10.1080/10426509008038056>
• Swamy K. C. Kumara, Burton Sarah D., Holmes Joan M., Day Robehta O., Holmes Robert R.: Cyclic Oxyphosphoranes with Six- and Seven-Membered Rings. Phosphorus Sulfur Silicon Relat Elem 1990, 49-50, 367. <http://dx.doi.org/10.1080/10426509008038981>
• Breuer E., Karaman R., Gibson D., Goldblum A.: Structure and Reactivity of 2-Hydroxyiminobenzyl-2-oxo-4,4,5,5-tetramethyl[1,3,2]dioxaphospholanes. Phosphorus Sulfur Silicon Relat Elem 1989, 41, 433. <http://dx.doi.org/10.1080/10426508908039733>
• Cedergren Robert, Lang B.Franz, Gravel Denis: A mechanism for the RNA-catalyzed formation of 5′-phosphates The origin of nucleases. FEBS Letters 1987, 226, 63. <http://dx.doi.org/10.1016/0014-5793(87)80551-3>
• Wróblewski Andrzej E.: Analogues of branched-chain tetrafuranosides having phosphorus in the anomeric position. Tetrahedron 1986, 42, 3595. <http://dx.doi.org/10.1016/S0040-4020(01)87326-9>
• Corriu Robert J.P, Lanneau Gerard F., Leclercq Dominique: Investigations of the nucleophilic displacement at the tetrahedral phosphorus - kinetic effects of the nucleophile for a given stereochemistry. Tetrahedron 1986, 42, 5591. <http://dx.doi.org/10.1016/S0040-4020(01)88163-1>
• Märkl G., Alig B.: Zur chemie des cyclooctatetraenyldilithiums. J Organomet Chem 1984, 273, 1. <http://dx.doi.org/10.1016/0022-328X(84)80503-3>
• Wróblewski A.E.: Stereochemistry of 1,2-oxaphospholanes—I. Tetrahedron 1983, 39, 1809. <http://dx.doi.org/10.1016/S0040-4020(01)88692-0>
• Corriu Robert J.P., Lanneau Gérard F., Leclercq Dominique: Silicon-phosphorus analogies rate controlling factors in SN2(P) reactions influence of the nucleophile for a given stereochemistry. Tetrahetron Lett 1983, 24, 4323. <http://dx.doi.org/10.1016/S0040-4039(00)88331-8>
• Larsen Rolf Olaf, Aksnes Gunnar: KINETIC STUDY OF THE HORNER-REACTION. I. Phosphorous and Sulfur and the Related Elements 1983, 15, 219. <http://dx.doi.org/10.1080/03086648308073297>
• Heesing Albert, Steinkamp Heinz: Mechanismen bei elektrophilen Reaktionen von reaktiven Stickstoffverbindungen mit Phosphanen. Chem Ber 1982, 115, 2854. <http://dx.doi.org/10.1002/cber.19821150816>
• Bouchu D., Dreux J.: SYNTHESIS OF DIASTEREOISOMERIC 2,4,7-TRIOXA-3-PHOSPHA-3-R-3-THIONOBICYCLO (4.4.0) DECANES AS A MODEL FOR PHOSPHORUS NUCLEOPHILIC SUBSTITUTION STUDIES. Phosphorous and Sulfur and the Related Elements 1982, 13, 25. <http://dx.doi.org/10.1080/03086648208078979>
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