The solvolyses of 5-norbornen-2-yl esters have posed a considerable problem in interpretation, especially since there are divergences between the reported results. 1,2,3 Recently, It has been suggested on the basis of a tritium labeling study that the process involves a pair of enantiomeric homoall
β¦ LIBER β¦
Secondary .beta.-deuterium effects on the rates of solvolyses of benzonorbornen-2(exo)- and -2(endo)-yl p-bromobenzenesulfonates
β Scribed by Tanida, Hiroshi; Tsushima, Tadahiko
- Book ID
- 126419073
- Publisher
- American Chemical Society
- Year
- 1971
- Tongue
- English
- Weight
- 811 KB
- Volume
- 93
- Category
- Article
- ISSN
- 0002-7863
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