REACTIVITY OF METHYLENETRIPHENYLPHOSPHORANES HAVING TWO PHENYL GROUPS CONSTRAINED WITH ETHANO OR ETHENO BRIDGE

References

• Maercker , A. 1965 . Organic Reactions , Edited by: Cope , A. C. Vol. 14 , 272 New York : John Wiley & Sons .
   Google Scholar
• Brown , G. W. , Cookson , R. C. and Stevens , I. D. R. 1964 . Tetrahedron Lett. , : 1263
   Google Scholar
• Sullivan , W. W. , Ullman , D. and Shechter , H. 1969 . Tetrahedron Lett. , : 457
   Google Scholar
• Schonberg , A. , Singer , E. and Schulze-Pannier , H. 1973 . Chem. Ber. , 106 : 2663
   Google Scholar
• Sidky , M. M. and Boulos , L. S. 1984 . Phosphorus. Sulfur and Silicon , 19 : 27
   Web of Science ®Google Scholar
• Okuma , K. , Shimasaki , M. , Kojima , K. , Ohta , H. and Okazaki , R. 1993 . Chem. Lett. , 1599
   Google Scholar
• Johnson , A. W. and LaCount , R. B. 1960 . Tetrahedron , 9 : 130
   Google Scholar
• Kawamura , Y. , Sato , Y. , Horie , T. and Tsukayama , M. 1997 . Tetrahedron Left. , 38 : 7893
   Web of Science ®Google Scholar
• Kawamura , Y. , Ohama , T. and Horie , T. International Chemical Congress of Pasific Basin Societies . December 17–22 , Honolulu, USA. ORGN 535
   Google Scholar
• Staudinger , H. and Meyer , J. 1919 . Helv. Chim. Acra , 2 : 635
   Web of Science ®Google Scholar
• Pinck , L. A. and Hilbert , G. E. 1947 . J. Am. Chem. Soc. , 69 : 723
   PubMed Web of Science ®Google Scholar
• Salisbury , L. 1970 . J. Org. Chem. , 35 : 4258
   Google Scholar
• Bergmann , E. D. , Berthier , G. , Fischer , E. , Hirshberg , Y. , Lavie , D. , Loewenthal , E. and Pullman , B. 1952 . Bull. Soc. Chim. Fr. , 78
   Google Scholar
• Sidky , M. M. and Boulos , L. S. 1984 . Phosphorus, Sulfur and Silicon , 19 : 27
   Web of Science ®Google Scholar
• Sidky , Mahran , M. R. and Boulos , L. S. 1980 . Phosphorus, Sulfur and Silicon , 8 : 365
   Web of Science ®Google Scholar
• Boulos , L. S. and Sidky , M. M. 1983 . Egypt. J. Chem. , 26 : 547
   Google Scholar
• Bestrnann , H. J. and Lang , H. J. 1969 . Tetrahedron Lett. , 2101
   Google Scholar
• Stewart , J. J. P. 1989 . J. Comput. Chem. , 10 : 221 Computer claculations were carried out using the CAChe-MOPAC program (Release 6.1) available from Sony-Tektronix, Co. Semiempirical PM3 SCF-MO calculations were executed
   Web of Science ®Google Scholar
• Johnson , A. W. 1959 . J. Org. Chem. , 24 : 282 The dipole moment of fluorenylidenetriphenyl derivative measured in benzene at 25°C, was reported as 7.09 D
   Web of Science ®Google Scholar
• Butterfield , P. J. , Tebby , J. C. and King , T. J. 1978 . J. Chem. Soc., Perkin , 1 : 1237
   Google Scholar
• Albrigbt , T. A. , Gordon , M. D. , Freeman , W. J. and Schweizer , E. E. 1976 . J. Am. Chem. Soc. , 98 : 6249
   Google Scholar
• Günther , H. 1994 . NMR Spectroscopy, , 2nd ed. , 496 – 501 . Chichester : John Wiley & Sons . Chap. 11
   Google Scholar
• Berti , G. 1957 . J. Org. Chem. , 22 : 230
   Google Scholar
• Bellucci , G. , Chiappe , C. , Marioni , F. and Marchetti , F. 1991 . J. Phys. Org. Chem. , 4 : 387 Melting point was apparently different from our data. Published data seemed to be the data of the precursor, 5-dibenzosuberenol (mp 119 °C)
   Google Scholar