A Convenient Synthesis of 2-Phenylindene

References

• Braun , J. V. and Mantz , M. 1929 . Ber. , 62 : 1062
   Google Scholar
• Platter , P. A. , Sandrin , R. and Wyss , J. 1946 . Helv. Chirn. Acta , 29 : 1604 1606
   Google Scholar
• Mayer , E. , Sieglitz and Ludering , W. 1921 . Ber. , 54 : 1400
   Google Scholar
• Cantrell , T. S. and Shachter , H. 1967 . J. Am. Chem. Soc. , 89 : 5869
   Google Scholar
• Glaton , S. A. , Kalafer , M. and Bringer , F. M. 1970 . J. Org. Chem. , 35 : 1
   PubMedGoogle Scholar
• Bendall , V. I. and Dharmoshi , S. S. 1972 . J. Chem. Soc. Perkin. 1 , 21 : 2732
   Google Scholar
• Jayamani , M. and Pillai , C. N. 1984 . J. Catal. , 87 : 93
   Google Scholar
• Jayamani , M. , Viswanathan , B. and Pillai , C. N. 1984 . J. Catal. , 89 : 560 Alumina catalyst was prepared by the hydrolysis of aluminium isopropoxide by the moisture present in air. For details of preparation, see Ref. Alumina catalyst prepared by methods other than the above gave poor results
   Google Scholar
• NMR of 2-phenylindene, [sgrave] 3.7(s,2H),6.9–7.5(m, 10H) and 3-phenylindene [sgrave] 3.2(d,2H), 6.15(t,1H), 6.8–7.3(m,9H); NMR of a 1:1 mixture of 2- and 3-phenylindene gives the following signals: ò 3.35(d,2H), 3.6(s,3H), 6.3(t,1H) 6.8–7.8 (m,9H), the shift in value is probably due to association
   Google Scholar
• Parham , W. E. and Wright , W. D. 1957 . J. Org. Chem. , 22 : 1473
   Google Scholar
• Braun , V. and Manz . 1929 . Ber. , 62 : 1059
   Google Scholar
• Vorlander and Siebert . 1906 . Ber. , 39 : 1024
   Google Scholar
• Vaillant , M. 1954 . Ann. Chim. , 9 : 5
   Google Scholar