Catalysis of a free radical allylic displacement by allyl iodide
Joint Authors
Mahdi, Jasim G.
Dawud, Hanna M.
Kelly, David R.
Source
Journal of Saudi Chemical Society
Issue
Vol. 13, Issue 3 (31 Dec. 2009), pp.291-293, 3 p.
Publisher
Publication Date
2009-12-31
Country of Publication
Saudi Arabia
No. of Pages
3
Main Subjects
Abstract EN
The preparation of ally chlorostannan 5 was achieved into two steps via free radical displacement of the sulphone group by tributyltin radical.
The chemical structure of compound 5 was confirmed by normal spectroscopic methods, including NMR, IR and MS.
The mechanism for the free radical reaction of chlorosulphone 6 with tributyltinhydride is likely to proceed via the catalysis of the trace amount of the ideally chloride 4.
American Psychological Association (APA)
Mahdi, Jasim G.& Dawud, Hanna M.& Kelly, David R.. 2009. Catalysis of a free radical allylic displacement by allyl iodide. Journal of Saudi Chemical Society،Vol. 13, no. 3, pp.291-293.
https://search.emarefa.net/detail/BIM-250836
Modern Language Association (MLA)
Mahdi, Jasim G.…[et al.]. Catalysis of a free radical allylic displacement by allyl iodide. Journal of Saudi Chemical Society (Mar. 2009), pp.291-293.
https://search.emarefa.net/detail/BIM-250836
American Medical Association (AMA)
Mahdi, Jasim G.& Dawud, Hanna M.& Kelly, David R.. Catalysis of a free radical allylic displacement by allyl iodide. Journal of Saudi Chemical Society. 2009. Vol. 13, no. 3, pp.291-293.
https://search.emarefa.net/detail/BIM-250836
Data Type
Journal Articles
Language
English
Notes
Includes bibliographical references : p. 293
Record ID
BIM-250836