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Cyclisierungsreaktionen β,γ-ungesättigter Kohlensäurederivate. XI [1] Untersuchungen zur Stereochemie der Cyclofunktionalisierung β,γ-ungesättigter Carbamidsäureester

✍ Scribed by Prof. Dr. M. Mühlstädt; Dipl.-Chem. R. Meusinger; B. Olk; Dr. L. Weber; Dr. R. Widera


Publisher
John Wiley and Sons
Year
1986
Tongue
English
Weight
274 KB
Volume
328
Category
Article
ISSN
1615-4150

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📜 SIMILAR VOLUMES


Cyclisierungsreaktionen β, γ-ungesättigt
✍ Prof. Dr. M. Mühlstädt; Dr. R. Widera 📂 Article 📅 1980 🏛 John Wiley and Sons 🌐 English ⚖ 522 KB

**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‐o

Cyclisierungsreaktionen β,γ-ungesättigte
✍ Prof. Dr. M. Mühlstädt; Dr. R. Widera; Dipl.-Chem. B. Olk 📂 Article 📅 1982 🏛 John Wiley and Sons 🌐 English ⚖ 417 KB

**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-ungesättigt
✍ Prof. Dr. M. Mühlstädt; Dr. R. Widera 📂 Article 📅 1981 🏛 John Wiley and Sons 🌐 English ⚖ 460 KB

**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

Cyclisierungsreaktionen β,γ-ungesättigte
✍ Dr. R. Widera; Prof. Dr. M. Mühlstädt 📂 Article 📅 1982 🏛 John Wiley and Sons 🌐 English ⚖ 276 KB

**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