𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Reaction of chlorosulfonylthiolene- and -thiolane-1,1-dioxides with amines and hydroxycompounds

✍ Scribed by A. A. Tukhar'; Yu. V. Bezuglyi; V. P. Foremnaya; A. G. Bratunets; A. M. Shakhvorost

Publisher
Springer US
Year
1989
Tongue
English
Weight
342 KB
Volume
25
Category
Article
ISSN
0009-3122

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

The reaction of hydrogen atoms with 1-bu
The reaction of hydrogen atoms with 1-butanethiol and thiolane the role of chemically activated 1-butanethiol
✍ Osamu Horie; Junya Nishino; Akira Amano 📂 Article 📅 1978 🏛 John Wiley and Sons 🌐 English ⚖ 590 KB

## Abstract The reaction of 1‐butanethiol with hydrogen atoms has been studied at temperatures of 295° and 576° K under the pressure of 660 Pa, using a conventional discharge‐flow apparatus. The reaction products (besides hydrogen sulfide and methane) under the low conversion range (∼10%) consisted

Properties and Reactions of Substituted
Properties and Reactions of Substituted 1,2-Thiazetidine 1,1-Dioxides: 3-Acetoxy-1,2-thiazetidine 1,1-Dioxide, Synthesis and Reactions with C-Nucleophiles
✍ Schwenkkraus, Peter ;Merkle, Stefan ;Otto, Hans-Hartwig 📂 Article 📅 1997 🏛 John Wiley and Sons 🌐 English ⚖ 670 KB

## 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

Ring-Enlargement and Ring-Opening Reacti
Ring-Enlargement and Ring-Opening Reactions of 1,2-Thiazetidin-3-one 1,1-Dioxides with Ammonia and Primary Amines as Nucleophiles
✍ Tonya R. Todorova; Anthony Linden; Heinz Heimgartner 📂 Article 📅 1999 🏛 John Wiley and Sons 🌐 German ⚖ 264 KB 👁 1 views

The N-benzyl-and N-alkyl-substituted 1,2-thiazetidin-3-one 1,1-dioxides 1b ± d reacted readily with NH 3 and primary amines via ring opening. The reaction with NH 3 proceeded at À 788 3 room temperature yielding ring-opened adducts via nucleophilic attack of NH 3 at the sulfonyl group, whereas the r