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.
📜 SIMILAR VOLUMES
Solventless reactions are currently a subject of extensive interest in both inorganic and organic chemistry. [1] In particular, organic synthesis may benefit from avoiding the use of organic solvents, yet this is valid only if a whole process, including work-up operations, is free from organic solve