CrossRef enabled

PAC Archives

Archive →

Pure Appl. Chem., 1987, Vol. 59, No. 12, pp. 1605-1612

http://dx.doi.org/10.1351/pac198759121605

Stereoelectronic effects on bond length and reactivity

A. J. Kirby

CrossRef Cited-by theme picture

CrossRef Cited-by Linking

  • Lazareva N. F., Lazarev I. M.: Electronic effects of 2-azasilatran-3-one groups. Russ J Gen Chem 2013, 83, 1649. <http://dx.doi.org/10.1134/S1070363213090041>
  • Roversi Elena, Scopelliti Rosario, Solari Euro, Estoppey Raphaël, Vogel Pierre, Braña Pedro, Menéndez Bibiana, Sordo José A.: The Hetero-Diels-Alder Addition of Sulfur Dioxide to 1-Fluorobuta-1,3-dienes: The Sofa Conformations Preferred by 6-Fluorosultines (6-Fluoro-3,6-dihydro-1,2-oxathiin-2-oxides) Enjoy Enthalpic and Conformational Anomeric Effects. Chem Eur J 2002, 8, 1336. <http://dx.doi.org/10.1002/1521-3765(20020315)8:6<1336::AID-CHEM1336>3.0.CO;2-R>
  • Jochem Georg, Breitsameter Florian, Schier Annette, Schmidpeter Alfred: Structure and dissociation of ylidyl chlorophosphanes. Heteroatom Chem 1996, 7, 239. <http://dx.doi.org/10.1002/(SICI)1098-1071(199608)7:4<239::AID-HC5>3.0.CO;2-0>
  • Schick Gerold, Loew Armin, Nieger Martin, Niecke Edgar: On the reaction of aminobis(diorganylamino)phosphanes with halogenophosphanes—P-hydrogeno(iminophosphoranyl)-halogenophosphanes and P-hydrogeno(iminophosphoranyl)-σ2, λ3-iminophosphanes. Heteroatom Chem 1996, 7, 427. <http://dx.doi.org/10.1002/(SICI)1098-1071(199611)7:6<427::AID-HC5>3.0.CO;2-5>
  • Schrödel Hans-Peter, Jochem Georg, Schmidpeter Alfred, Nöth Heinrich: Yliddiyl-halogenphosphan-Oligomere (Ph3PCPX)n – eine strukturell vielfältige Verbindungsfamilie. Angew Chem 1995, 107, 2006. <http://dx.doi.org/10.1002/ange.19951071714>
  • Schmidpeter Alfred, Nöth Heinrich, Jochem Georg, Schrödel Hans-Peter, Karaghiosoff Konstantin: Ylidyl-dihalogenphosphane – Strukturbilder einer sich anbahnenden Dissoziation. Chem Ber 1995, 128, 379. <http://dx.doi.org/10.1002/cber.19951280410>
  • 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>
  • Grützmacher Hansjörg, Pritzkow Hans: Drei unabhängige Moleküle in der Elementarzelle eines Phosphor-Ylids; Änderungen der Molekülgeometrie bei der Rotation um die Phosphor-Kohlenstoff-Ylidbindung. Angew Chem 1992, 104, 92. <http://dx.doi.org/10.1002/ange.19921040131>
  • Dubois Jacques-Emile, Cossé-Barbi Aliette: Strain release in conformational and geometric adaptation of moderately and highly congested systems: Interplay of small structural effects. Struct Chem 1991, 2, 89. <http://dx.doi.org/10.1007/BF00676620>
  • Katritzky Alan R., Luce Hudson H., Anders Ernst, Sullivan John M.: Experimental test of structural predictions of semiempirical methods: Bis (1,2-dioxa-4,6-diazacycloheptano)[4′,5′,6′: 1,6,5][4″,5″,6″: 2,3,4]-1,2,4,5-tetraazacyclohexane, A 7:6:7-Tricyclic system correctly calculated by AM1 as more stable than its 6:6:6-Tricyclic isomer. Chem Ber 1989, 122, 1989. <http://dx.doi.org/10.1002/cber.19891221026>
  • Böhm Karin, Gössinger Edda, Müller Renate: A versatile regio- and stereospecific annulation method - II. Tetrahedron 1989, 45, 1391. <http://dx.doi.org/10.1016/0040-4020(89)80137-1>