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

Saudi Chemical Society

Publication Date

2009-12-31

Country of Publication

Saudi Arabia

No. of Pages

3

Main Subjects

Chemistry

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