Letters to Editor
nature 156, 53-53 (14 July 1945) | doi:10.1038/156053a0
Halogenation in the Allyl Position
WILLIAM E. VAUGHAN , FREDERICK F. RUST & GEORGE W. HEARNE
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WE should like to make a few comments on the recent communication by W. A. Waters1 in criticism of F. S. Spring2 for stating that substitution in the allyl position of olefines is a new reaction attributable to Ziegler and his collaborators3.
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References
- Nature, 154, 772 (1944).
- Annual Reports of the Chemical Society, 40, 101 (1943).
- Annalen der Chemie, 551, 80 (1942).
- Groll and Hearne, Ind. Eng. Chem., 31, 1530 (1939). Engs and Redmond, U.S. Patent 2,077,382, April 20, 1937. Groll, Hearne, Burgin and LaFrance, U.S. Patent 2,130,084, September 13, 1938.
- Trans. Faraday Soc., 38, 340 (1942).
- J. Org. Chem., 5, 472 (1940).
- Trans. Faraday Soc., 37, 791 (1941).
- Trans. Faraday Soc., 37, 792 (1941).
- See Mayo and Walling, Chem. Rev., 87, 351 (1940).
- Vaughan and Rust, J. Org. Chem., 7, 472, 477 (1942).
- See, for example, ref. (9), (p. 358); also, Weiss, Trans. Faraday Soc., 37, 793 (1941).
- For example, see references (5) and (8).
