Lactonization of methyl 4-aryl-5-tosyloxyhexanoate via a phenonium ion
โ Scribed by Shinji Nagumo; Tomoaki Hisano; Yo-ichiro Kakimoto; Norio Kawahara; Machiko Ono; Tsuneo Furukawa; Sanae Takeda; Hiroyuki Akita
- Publisher
- Elsevier Science
- Year
- 1998
- Tongue
- French
- Weight
- 224 KB
- Volume
- 39
- Category
- Article
- ISSN
- 0040-4039
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โฆ Synopsis
Lactonization of methyl 4-atyl-5-tosyloxy hexanoate 3 via a phenonium ion gave 7 -lactone 4 selectively under thermodynamical conditions while it afforded 6-1actone 5 preferentially under kinetic conditions.
๐ SIMILAR VOLUMES
## Abstract A facile highly regioselective process is described for the formation of 4โchloromethylโ1,3โoxazoles from 1,3โoxazole __N__โoxide/HCl salts. An explanation is presented for the high regioselectivity in deoxygenationโchlorination using POCl~3~ with HCl salts compared to the corresponding