✦ LIBER ✦

2-Dimethylcarbamoyl-1,3,2-dioxazolidine, 2-dimethylcarbamoyl- and 2h-perhydro-1,3,2-dioxazines

✍ Scribed by V. F. Rudchenko; V. I. Shevchenko; R. G. Kostyanovskii

Book ID: 112443325
Publisher: Springer
Year: 1985
Tongue: English
Weight: 92 KB
Volume: 34
Category: Article
ISSN: 1573-9171
DOI: 10.1007/bf00950173

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Conformational transformations of perhyd

Conformational transformations of perhydro-1,3,2-dioxazine

✍ Kuznetsov, V. V. 📂 Article 📅 2012 🏛 Springer 🌐 English ⚖ 139 KB

Conformational preference of perhydro-1,

Conformational preference of perhydro-1,3,2-dioxazine inside nanotubes

✍ Kuznetsov, V. V. 📂 Article 📅 2014 🏛 Springer 🌐 English ⚖ 582 KB

Methyl 1,6-dihydro-1-(dimethylcarbamoyl)

Methyl 1,6-dihydro-1-(dimethylcarbamoyl)-4-methyl-6-oxo-2-phenyl-3-pyridinecarboxylate

✍ Pilati, T. 📂 Article 📅 1990 🏛 International Union of Crystallography 🌐 English ⚖ 348 KB

2,4-Bis(dimethylcarbamoyl)-1,1-dioxo-3-p

2,4-Bis(dimethylcarbamoyl)-1,1-dioxo-3-phenyl-1λ6,2,4,3-thiadiazaboretidin: Ein BN2S-Ring durch „Einschiebungsreaktion” von Sulfonyldiisocyanat

✍ Prof. Dr. Herbert W. Roesky; Dr. Sushil K. Mehrotra 📂 Article 📅 1978 🏛 John Wiley and Sons 🌐 English ⚖ 225 KB 👁 1 views

Die aktivierten Ester ( 4 ) liefern sowohl rnit Aminosaureestern als auch rnit Aminosaureester-hydrogenchloriden/Triethylamin bei -10 bis 0°C innerhalb weniger Stunden die N-Acylpeptidester (5)131 in sehr hohen Ausbeuten''] (Tabelle 2).

2,4-Bis(dimethylcarbamoyl)-1,1-dioxo-3-p

2,4-Bis(dimethylcarbamoyl)-1,1-dioxo-3-phenyl-1λ6,2,4,3-thiadiazaboretidine: a BN2S Ring by “Insertion” of Sulfonyl Diisocyanate

✍ Prof. Dr. Herbert W. Roesky; Dr. Sushil K. Mehrotra 📂 Article 📅 1978 🏛 John Wiley and Sons 🌐 English ⚖ 122 KB 👁 1 views

(2S,3aR,7aR)-Perhydro-1H-1,3-benzimidazo

(2S,3aR,7aR)-Perhydro-1H-1,3-benzimidazol-1-ium-2-carboxylate

✍ Biskupska, Inga ;Jaruta, Katarzyna ;Gdaniec, Maria 📂 Article 📅 2006 🏛 International Union of Crystallography 🌐 English ⚖ 195 KB

The title compound, C 8 H 14 N 2 O 2 , exists in the solid state in a zwitterionic form. The imidazolidinium fragment adopts an envelope conformation. The carboxylate group is involved in an intramolecular N + -HÁ Á ÁO À hydrogen bond.