Ring Openings of Substituted Cyclobutanes Induced by Grignard Reagents. II. 2,2,4,4-Tetramethyl-3-dimethylaminocyclobutanone *
β Scribed by Weintraub, Leonard; Wilson, Armin; Goldhamer, David L.; Hollis, Donald P.
- Book ID
- 127038046
- Publisher
- American Chemical Society
- Year
- 1965
- Tongue
- English
- Weight
- 543 KB
- Volume
- 30
- Category
- Article
- ISSN
- 0022-3263
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
Starting fiom 5-unsubstituted or 5-alkyl-, aryl-, beteroarylsubstituted 3-diethylamino-4arylisothiazole 1 ,I-dioxides by base induced ring opening 3-alkoxypropenamidines were synthesized in excellent yields in a mild and effcient way. When 5-bromo-3-diethylamino-4~arylisothiazole 1,1dioxide was use
## 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
## Lewis Acid-Mediated SN2 Type Displacement by Grignard Reagents on Chiral Perhydropyrido[2, 3, 4]oxadiazine.