Steric accelerations of nucleophilic displacement and addition reactions by 2-t-butylbenzenthiolate anion
β Scribed by Dorothy Semenow Garwood; Donald C. Garwood
- Book ID
- 104222511
- Publisher
- Elsevier Science
- Year
- 1970
- Tongue
- French
- Weight
- 203 KB
- Volume
- 11
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
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## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a βFull Textβ option. The original article is trackable v
The ring opening of 3-isopropyl-2-phenyl-3-oxetanol (2a) by (42% yield) and 26 (54% yield). Other 2-phenyl-3-oxetanols such as 2b and 2c can also be employed as electrophiles, various nucleophiles has been studied. In the presence of BF 3 as a Lewis acid, a clean reaction at the less substituted C-4