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The cause of the rate acceleration by diethyl ether solutions of lithium perchlorate (LPDE) in organic reactions. Application to high pressure synthesis

✍ Scribed by Gérard Jenner; Ridha Ben Salem


Publisher
Elsevier Science
Year
1997
Tongue
French
Weight
536 KB
Volume
53
Category
Article
ISSN
0040-4020

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✦ Synopsis


Kinetic ';tudies of isoprene c,,clodimenzation sh~ that the accelerating effect caused b 3 LPDE (soluti~m of lithium pcrchlorate in dieth~l ether) in some organic reactions canm~t be ascribed t~ internal pressure of LPDE. The kinetic effect is cssentiall 3 duc tt~ catal3sis through Li +. Addilional arguments are pro~ ided b 3 comparison o|" } ields obtained in LPDE ((). 1 MPa) and in organic s~l~ cnts (under pressure)lbr Diels-Alder reacti~ms of ~ ari<ms electronic t~ pcs. C~m~bination of high prcssure and LPDE catal3 sis is re~ ealed as an excellent multiacti~ atitm prc~cess tt~ achie~ c dilficult s3 ntheses, but ~ml~ for 14+2] cycloadditions.


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