With simple, aqueous acids, epoxides ring-open to give the anti 1,2-diol. ... Ring opening of epoxides by various nucleophiles is a very powerful tool in ...
www.chem.uky.edu/courses/che232/JEA/ln/4a.%20Ethers.pdf
(return to syllabus)
clem.mscd.edu/~wiederm/oc2chp/oc2chpethers/page8.htm
Ring strain makes epoxides more reactive than simple ethers. ... Epoxide chemistry will be discussed more in Chapter 16. ... Ring Opening of Epoxides...
www.mhhe.com/physsci/chemistry/carey/student/olc/graphi... www.mhhe.com/physsci/chemistry/carey/student/olc/graphics/carey04oc/ref/ch15ringopeningepoxides.html
Ring strain makes epoxides more reactive than simple ethers. ... Epoxide chemistry will be discussed more in Chapter 16. ... reaction of epoxide with organometallic reagents...
www.mhhe.com/physsci/chemistry/carey/student/olc/ch15ri... www.mhhe.com/physsci/chemistry/carey/student/olc/ch15ringopeningepoxides.html
reactivity of the epoxides by ring-opening can be enhanced ..... nucleophile for epoxide ring opening reactions due to its low ...
www.bentham.org/coc/sample/coc9-1/0001D.pdf
Epoxide - Wikipedia, the free encyclopedia
An epoxide is a cyclic ether with three ring atoms. This ring approximately defines an equilateral triangle, which makes it highly strained. The strained ring makes epoxides more reactive than other...
en.wikipedia.org/wiki/Epoxide
Akbar Heydari*, Morteza Mehrdad, Aziz Maleki, Nafiseh Ahmadi ... *Chemistry Department, Tarbiat Modarres University, P. O. Box 14155-4838, Tehran, Iran, Email: akbar.heydari gmx.de ... see article for more examples...
www.organic-chemistry.org/abstracts/literature/340.shtm
Author Topic: Non-terminal epoxide ring opening (Lewis acid catalysts) (Read 581 times) ... There is some little information about metal salen complexes that can work for general epoxide ring opening, but most of them either make a selective opening to OH,OH or other types.
www.chemicalforums.com/index.php?topic=35420.0
The Medscape Journal ... Allergy & Clinical Immunology ... Diabetes & Endocrinology...
www.medscape.com/medline/abstract/15599916
Reaction of aniline with various glycidic ethers gave the amino alcohols by regioselective nucleophilic attack at the terminal carbon atom of the epoxide ring as the only/major product. Zinc(II) perchlorate hexahydrate was found to be the best catalyst compared to other metal perchlorates.
www.medscape.com/medline/abstract/17411096