✦ LIBER ✦

The Condensation Reaction between Sulfamide and Monoketones

✍ Scribed by Ouchi, Akira; Moeller, Therald

Book ID: 121338304
Publisher: American Chemical Society
Year: 1964
Tongue: English
Weight: 297 KB
Volume: 29
Category: Article
ISSN: 0022-3263
DOI: 10.1021/jo01030a048

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Condensation between Formaldehyde and Mo

Condensation between Formaldehyde and Monoketones. II

✍ Matsumura, Konomu 📂 Article 📅 1935 🏛 American Chemical Society 🌐 English ⚖ 183 KB

CONDENSATIONS BETWEEN FORMALDEHYDE AND M

CONDENSATIONS BETWEEN FORMALDEHYDE AND MONOKETONES. I. CONDENSATION OF 5-ACETYL-8-HYDROXYQUINOLINE WITH ALDEHYDES

✍ Matsumura, Konomu.; Sone, Chusaburo. 📂 Article 📅 1931 🏛 American Chemical Society 🌐 English ⚖ 190 KB

Monoketones as Acceptors in the Oxyphosp

Monoketones as Acceptors in the Oxyphosphorane Carbon—Carbon Condensation. Condensation of α Diketones with Monoketones and with Perfluoro Ketones. P 31 Nuclear Magnetic Resonance Spectra 1,2

✍ Ramirez, Fausto; Patwardhan, A. V.; Smith, C. P. 📂 Article 📅 1966 🏛 American Chemical Society 🌐 English ⚖ 845 KB

The elimination-condensation reaction be

The elimination-condensation reaction between dimethylaluminum hydride and methylphenylphosphine

✍ Beachley, O. T.; Victoriano, L. 📂 Article 📅 1986 🏛 American Chemical Society 🌐 English ⚖ 616 KB

Condensation Reaction Between α-Amino Ac

Condensation Reaction Between α-Amino Acid Phenylhydrazides and Carbonyl Compounds.

✍ Giancarlo Verardo; Paola Geatti; Paolo Martinuzzi; Marcello Merli; Nicoletta Ton 📂 Article 📅 2004 🏛 John Wiley and Sons ⚖ 179 KB

Condensation Reaction Between α-Amino Ac

Condensation Reaction Between α-Amino Acid Phenylhydrazides and Carbonyl Compounds

✍ Giancarlo Verardo; Paola Geatti; Paolo Martinuzzi; Marcello Merli; Nicoletta Ton 📂 Article 📅 2003 🏛 John Wiley and Sons 🌐 English ⚖ 178 KB

## Abstract The natural α‐amino acid phenylhydrazides **1a**−**d** readily react with the aldehydes **2a**−**d** and ketones **2e**−**h** to produce the 3‐(phenylamino)imidazolidin‐4‐one derivatives **4** in good yields. Their structures were confirmed by X‐ray structural analysis. Polycyclic syste