Organic Synthesis Involving Multipolymer Reactions. Polymeric Trityllithium

Journal of the American Chemical Society

Volumn 99, Issue 12, 1977, Pages 4165-4167

  Cohen, B J ^a   Kraus, M A ^a   Patchornik, A ^a  

^a WEIZMANN INSTITUTE OF SCIENCE   (Israel)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 33847089129     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/ja00454a050     Document Type: Article

References (12)

1. Dedicated to Professor R. B. Woodward on the occasion of his 60th birthday.
2. A preliminary account of part of this work was presented at the 172nd National Meeting of the American Chemical Society, San Francisco, Calif., Aug 1976. See A. Patchornik, Polym. Prepr., Am. Chem. Soc., Div. Polym., 17,213 (1976).
3. C. G. Overberger and K. N. Sannes, Angew. Chem., Int. Ed. Engl., 13, 99 (1974).
4. C. C. Leznoff, Chem. Soc. Rev., 3, 65 (1974).
5. A. Patchornik and M. A. Kraus, Pure Appl. Chem., 43, 503 (1975).
6. M. A. Kraus and A. Patchornik, J. Am. Chem. Soc., 93, 7325 (1971).
7. J. Rebek and F. Gavina, J. Am. Chem. Soc., 97, 3453 (1975).
8. C. U. Pittman and L. R. Smith, J. Am. Chem. Soc., 97, 1749 (1975).
9. A. Patchornik and M. A. Kraus, J. Am. Chem. Soc., 92, 7587 (1970).
10. Macroreticular XE-305 “Rohm and Haas” polystyrene was used. The commercial polymer was ground to particles of 100-150 mesh size.
11. For Friedel-Crafts alkylations of polystyrene, see A. Patchornik, R. Kalir, M. Fridkin, and A. Warshawsky, U.S. Patent 3 974 110 (Aug 10, 1976).
12. R. Kalir, M. Fridkin, and A. Patchornik, Eur. J. Biochem., 42, 151 (1974).