Abstract
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.
This is a preview of subscription content, access via your institution
Access options
Subscribe to this journal
Receive 51 print issues and online access
$199.00 per year
only $3.90 per issue
Buy this article
- Purchase on SpringerLink
- Instant access to the full article PDF.
USD 39.95
Prices may be subject to local taxes which are calculated during checkout
Similar content being viewed by others
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).
Author information
Authors and Affiliations
Rights and permissions
About this article
Cite this article
VAUGHAN, W., RUST, F. & HEARNE, G. Halogenation in the Allyl Position. Nature 156, 53 (1945). https://doi.org/10.1038/156053a0
Issue date:
DOI: https://doi.org/10.1038/156053a0


