## Abstract The 1,2‐dithiolosultam derivative 14 was obtained from the (__α__‐bromoalkylidene)propenesultam derivative 9 (__Scheme 1__). Regioselective cleavage of the two ester groups (→1b or 2b) allowed the preparation of derivatives with different substituents at C(3) in the dithiole ring (see 2
Direct synthesis of trisubstituted isothiazole 1,1-dioxides. Regioselective substitution reactions at C-3 and C-4
✍ Scribed by Britcher, Susan F.; Cochran, David W.; Phillips, Brian T.; Springer, James P.; Lumma, William C.
- Book ID
- 120045622
- Publisher
- American Chemical Society
- Year
- 1983
- Tongue
- English
- Weight
- 637 KB
- Volume
- 48
- Category
- Article
- ISSN
- 0022-3263
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
## Abstract __N__‐Silylated 3‐acetoxy‐1,2‐thiazetidine 1,1‐dioxide (5) is prepared from L‐cystine. Reactions of 5 with silyl enol ethers yield C‐3‐substituted β‐sultams 6, 12 and 15. Desilylation of 6 affords 7, which undergoes photochemical cyclization to give the bicyclic β‐sultam 10. In the cour
## Abstract The introduction of functional groups at the 4‐position of the __β__‐sultam ring was realized by the synthesis of mono‐ and disubstituted derivatives by reactions of __N__‐silylated __β__‐sultams with electrophiles in the presence of BuLi or LDA. As electrophiles, ketones, chlorosilanes