**Cyclization Reactions of β,γ‐Unsaturated Derivatives of Carbonic Acid. V. Reactions of β,γ‐Unsaturated Carbamic Acid Esters with Sulfenyl Chlorides — Synthesis of 3,5,5‐Trisubstituted Oxazolidine‐2‐ones** N,N‐Disubstituted β,γ‐Unsaturated urethanes **1** have been cyclized to 3,5,5‐trisubstituted
Cyclisierungsreaktionen β, γ-ungesättigter Kohlensäurederivate. II. Reaktionen β, γ-ungesättigter Carbamidsäurederivate mit elektrophilen Reagenzien - Synthese von N-substituierten Oxazolidin-2-onen
✍ Scribed by Prof. Dr. M. Mühlstädt; Dr. R. Widera
- Publisher
- John Wiley and Sons
- Year
- 1980
- Tongue
- English
- Weight
- 522 KB
- Volume
- 322
- Category
- Article
- ISSN
- 1615-4150
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✦ Synopsis
Cyclization Reactions of β,γ‐Unsaturated Derivatives of Carbonic Acid. II. Reactions of β,γ‐Unsaturated Carbamic Acid Esters with Electrophilic Reagents — Synthesis of N‐Substituted Oxazolidine‐2‐ones
N,N‐Disubstituted β,γ‐unsaturated urethans have been cyclized to N‐substituted oxazolidine‐2‐ones by dry hydrogen chloride in methylene chloride. The N‐substituted urethan 1a reacts with hydrogen chloride to form the urethan 2a and the 2‐oxazoline 3 Reaction of 1 with bromine yields the corresponding N‐substituted 5‐bromomethyl oxazolidine‐2‐ones 6
📜 SIMILAR VOLUMES
**Cyclization Reactions of β,γ‐Unsaturated Derivatives of Carbonic Acid. IV. Synthesis of N‐Substituted Thiazolidine‐2‐ones and 2‐Alkoxy‐2‐thiazolines from β,γ‐Unsaturated Thiocarbamic Acid Esters** The reaction between N‐substituted β,γ‐unsaturated thiourethans and dry hydrogen chloride or bromine
**Cyclization Reactions of β,γ‐Unsaturated Derivatives of Carbonic Acid. VII. Synthesis of Unequivocal N‐Acylated Thiazolidine‐2‐ones and Oxazolidine‐2‐ones** A new synthetic route to N‐acylated thiazolidine‐2‐ones and oxazolidine‐2‐ones is reported: The reaction of carboxylic acid chlorides with 2