The N-benzyl-and N-alkyl-substituted 1,2-thiazetidin-3-one 1,1-dioxides 1b Β± d reacted readily with NH 3 and primary amines via ring opening. The reaction with NH 3 proceeded at Γ 788 3 room temperature yielding ring-opened adducts via nucleophilic attack of NH 3 at the sulfonyl group, whereas the r
β¦ LIBER β¦
Nucleophilic ring-opening reactions of morpholin-2-ones. A resolution of dl-(secondary-alkyl)amines
β Scribed by Kashima, Choji; Harada, Kazuo
- Book ID
- 127347094
- Publisher
- American Chemical Society
- Year
- 1989
- Tongue
- English
- Weight
- 530 KB
- Volume
- 54
- Category
- Article
- ISSN
- 0022-3263
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